Chemical Research in 2834-05-1

This compound(11-Bromoundecanoic acid)Computed Properties of C11H21BrO2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Computed Properties of C11H21BrO2. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 11-Bromoundecanoic acid, is researched, Molecular C11H21BrO2, CAS is 2834-05-1, about Evaluation of diuretic activity of crude extracts of leaves of filicium decipiens and analysis of biomolecules present in fraction of methanolic extract using GC-MS technique. Author is Basarikatti, A. I.; Uppar, V.; Padmashali, B..

Filicium decipiens belongs to the Sapindaceae family, which is commonly known as fern tree, is found in the Western Ghats of southern India, small highland areas of East Africa and Sri Lanka and it is a medium to a large evergreen tree. It is commonly cultivated in gardens and roadsides as ornamental, noise barriers and windbreak plant. Filicium decipiens traditionally used for the treatment of diabetes in India. The leaves of Filicium decipiens have been collected from the Western Ghats of southern India, shade dried and powd. well. The finely powd. leaves have been extracted with petroleum ether, chloroform, methanol and water successively with an increase in polarity. The methanolic extract was column chromate-graphed using silica gel G 100-200 mesh to get brown color crystalline solid, which was analyzed for the presence of bioactive chem. constituents using Gas chromatog.-mass spectrometry (GC-MS) technique. GC-MS anal. revealed the presence of thirty chem. constituents. The four different crude extracts (petroleum ether, chloroform, methanol and water) of leaves of Filicium decipiens have been tested with a diuretic activity using the Lipschitz method. The methanolic extract exhibits diuretic activity.

This compound(11-Bromoundecanoic acid)Computed Properties of C11H21BrO2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Flexible application of in synthetic route 2834-05-1

This compound(11-Bromoundecanoic acid)Product Details of 2834-05-1 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Goleva, Tatyana N.; Lyamzaev, Konstantin G.; Rogov, Anton G.; Khailova, Ljudmila S.; Epremyan, Khoren K.; Shumakovich, Galina P.; Domnina, Lidia V.; Ivanova, Olga Yu.; Marmiy, Natalia V.; Zinevich, Tatiana V.; Esipov, Dmitry S.; Zvyagilskaya, Renata A.; Skulachev, Vladimir P.; Chernyak, Boris V. published an article about the compound: 11-Bromoundecanoic acid( cas:2834-05-1,SMILESS:O=C(O)CCCCCCCCCCBr ).Product Details of 2834-05-1. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:2834-05-1) through the article.

An increase in the production of reactive oxygen species (ROS) in mitochondria due to targeted delivery of redox active compounds may be useful in studies of modulation of cell functions by mitochondrial ROS. Recently, the mitochondria-targeted derivative of menadione (MitoK3) was synthesized. However, MitoK3 did not induce mitochondrial ROS production and lipid peroxidation while exerting significant cytotoxic action. Here we synthesized 1,4-naphthoquinone conjugated with alkyltriphenylphosphonium (SkQN) as a prototype of mitochondria-targeted prooxidant, and its redox properties, interactions with isolated mitochondria, yeast cells and various human cell lines were investigated. According to electrochem. measurements, SkQN was more active redox agent and, due to the absence of Me group in the naphthoquinone ring, more reactive as electrophile than MitoK3. SkQN (but not MitoK3) stimulated hydrogen peroxide production in isolated mitochondria. At low concentrations, SkQN stimulated state 4 respiration in mitochondria, decreased membrane potential, and blocked ATP synthesis, being more efficient uncoupler of oxidative phosphorylation than MitoK3. In yeast cells, SkQN decreased cell viability and induced oxidative stress and mitochondrial fragmentation. SkQN killed various tumor cells much more efficiently than MitoK3. Since many tumors are characterized by increased oxidative stress, the use of new mitochondria-targeted prooxidants may be a promising strategy for anticancer therapy.

This compound(11-Bromoundecanoic acid)Product Details of 2834-05-1 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Chemical Research in 2834-05-1

This compound(11-Bromoundecanoic acid)Application In Synthesis of 11-Bromoundecanoic acid was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 2834-05-1, is researched, SMILESS is O=C(O)CCCCCCCCCCBr, Molecular C11H21BrO2Journal, Article, Angewandte Chemie, International Edition called Fabrication of Gradient and Patterned Organic Thin Films by Bipolar Electrolytic Micelle Disruption Using Redox-Active Surfactants, Author is Zhou, Yaqian; Shida, Naoki; Tomita, Ikuyoshi; Inagi, Shinsuke, the main research direction is organic thin film electrolytic micelle disruption fabrication; bipolar electrochemistry; gradient and patterned films; micelle disruption; organic films.Application In Synthesis of 11-Bromoundecanoic acid.

Bipolar electrochem. could be regarded as a powerful approach for selective surface modification due to the beneficial feature that a wirelessly controllable potential distribution on bipolar electrodes (BPEs). Herein we report a bipolar electrolytic micelle disruption (BEMD) system for the preparation of shaped organic films. A U-shaped bipolar electrolytic system with a sigmoidal potential gradient on the BPE gave gradient-thin films including various interesting organic compounds, such as a polymerizable monomer, an organic pigment and aggregation induced emission (AIE) mols. The gradient feature was characterized by UV-Vis absorption, thickness measurements and surface morphol. anal. Corresponding patterned films were also fabricated using a cylindrical bipolar electrolytic setup that enables site-selective application of the potential on the BPE. Such a facile BEMD approach will open a long-term perspective with respect to organic film preparation

This compound(11-Bromoundecanoic acid)Application In Synthesis of 11-Bromoundecanoic acid was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

The important role of 2834-05-1

This compound(11-Bromoundecanoic acid)Reference of 11-Bromoundecanoic acid was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference of 11-Bromoundecanoic acid. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 11-Bromoundecanoic acid, is researched, Molecular C11H21BrO2, CAS is 2834-05-1, about Temperature-responsive star-shaped poly(2-ethyl-2-oxazoline) and poly(2-isopropyl-2-oxazoline) with central thiacalix[4]arene fragments: structure and properties in solutions. Author is Lezov, A. A.; Gubarev, A. S.; Podsevalnikova, A. N.; Senchukova, A. S.; Lebedeva, E. V.; Dudkina, M. M.; Tenkovtsev, A. V.; Nekrasova, T. N.; Andreeva, L. N.; Smyslov, R. Yu.; Gorshkova, Yu. E.; Kopitsa, G. P.; Radulescu, A.; Pipich, V.; Tsvetkov, N. V..

Temperature-responsive star-shaped poly(2-ethyl-2-oxazoline) (star-PETOX) and poly(2-isopropyl-2-oxazoline) (star-PIPOX) with arms grafted to the lower rim of thiacalix[4]arene were studied in solutions by viscometry, sedimentation velocity, light scattering, and small-angle neutron scattering. The experiments were carried out in water and THF solutions It was revealed that in THF, the studied polymers were present only as individual mols., while in aqueous solutions, in addition to individual mols., large polymer aggregates were found. Mol. characteristics of the star-PETOX and star-PIPOX samples were estimated; their behavior in THF and water was studied over a wide temperature range. It was established that a cloud point of the aqueous solution of star-PETOX (67 °C) is higher than that of a solution of star-PIPOX (35 °C). Comparison of the data obtained by dynamic light scattering and small-angle neutron scattering turned out to be fruitful in revealing all the structural levels of the organization of star-PETOX and star-PIPOX in aqueous solutions They include the level of the individual macromols. and the level of supramol. organization with a star-like architecture.

This compound(11-Bromoundecanoic acid)Reference of 11-Bromoundecanoic acid was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Archives for Chemistry Experiments of 2834-05-1

《Quaternary Ammonium Based Carboxyl Functionalized Ionic Liquid for Covalent Immobilization of Horseradish Peroxidase and Development of Electrochemical Hydrogen Peroxide Biosensor》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)Related Products of 2834-05-1.

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Electroanalysis called Quaternary Ammonium Based Carboxyl Functionalized Ionic Liquid for Covalent Immobilization of Horseradish Peroxidase and Development of Electrochemical Hydrogen Peroxide Biosensor, Author is Murphy, Manoharan; Theyagarajan, K.; Thenmozhi, Kathavarayan; Senthilkumar, Sellappan, which mentions a compound: 2834-05-1, SMILESS is O=C(O)CCCCCCCCCCBr, Molecular C11H21BrO2, Related Products of 2834-05-1.

A novel electrochem. biosensor was developed using a judiciously designed platform for the rapid and accurate determination of hydrogen peroxide (H2O2). The horseradish peroxidase (HRP) based biosensor was constructed by covalent anchoring of the enzyme to a newly synthesized quaternary ammonium-based carboxyl functionalized ionic liquid (TBA-COOH-IL) immobilized on a multiwalled carbon nanotube deposited glassy carbon electrode (MWCNT/GCE). A stable amide bond is formed between HRP enzyme and IL by utilizing the terminal -NH2 of HRP and -COOH groups of TBA-COOH-IL, while the pi-pi stacking holds the TBA-COOH-IL firmly on the MWCNT/GCE and forms HRP/TBA-COOH-IL/MWCNT/GCE. Thus fabricated HRP/TBA-COOH-IL/MWCNT/GCE displayed a well-resolved redox peak at a formal potential (E°’) of -0.32 V, which corresponds to the concealed FeIII/FeII redox center of the immobilized HRP enzyme. Further, the developed biosensor was employed for the electrocatalytic determination of H2O2 in static and dynamic conditions, which showed a wide linear range from 0.02 to 4.30 mM with a high sensitivity and low detection limit of 160.6μA mM-1 cm-2 and 6μM, resp. The excellent performance of the fabricated biosensor is attributed to the stable covalent anchoring of freely water-soluble enzyme on the newly designed, highly conducting and biocompatible platform. Furthermore, the fabricated biosensor exhibited good reproducibility with an extended long-term stability.

《Quaternary Ammonium Based Carboxyl Functionalized Ionic Liquid for Covalent Immobilization of Horseradish Peroxidase and Development of Electrochemical Hydrogen Peroxide Biosensor》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)Related Products of 2834-05-1.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Little discovery in the laboratory: a new route for 2834-05-1

《Highly Chemoselective Esterification from O-Aminoallylation of Carboxylic Acids: Metal- and Reagent-Free Hydrocarboxylation of Allenamides》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)Electric Literature of C11H21BrO2.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 11-Bromoundecanoic acid( cas:2834-05-1 ) is researched.Electric Literature of C11H21BrO2.Pradhan, Tapas R.; Lee, Hae Eun; Gonzalez-Montiel, Gisela A.; Cheong, Paul Ha-Yeon; Park, Jin Kyoon published the article 《Highly Chemoselective Esterification from O-Aminoallylation of Carboxylic Acids: Metal- and Reagent-Free Hydrocarboxylation of Allenamides》 about this compound( cas:2834-05-1 ) in Chemistry – A European Journal. Keywords: trans acyloxyenamide preparation regioselective chemoselective diastereoselective green chem; allenamide carboxylic acid hydrocarboxylation aminoallylation; (E)-enamides; Brønsted acid; carboxylic acids; linear selective; metal-free. Let’s learn more about this compound (cas:2834-05-1).

Metal-free hydrocarboxylation of allenamides RCH=C=CH2 (R = N-benzyl(4-methylbenzene)sulfonamide, (methoxycarbonyl)(naphthalen-1-yl)aminyl, 2-oxo-1,3-oxazolidin-3-yl, etc.) with various functionalized carboxylic acids R1C(O)OH (R1 = Me, Ph, 1-(4-nitrophenyl)ethyl, 6-chloroimidazo[1,2-a]pyridin-3-yl, etc.) was achieved with complete regio- and stereocontrol (>49:1). This environmentally compatible transformation affords γ-acyloxyenamides RCH=CHCH2OC(O)R1 with exclusive E-selectivity. Electron rich, electron poor, aliphatic, aryl, and heterocyclic carboxylic acids all gave excellent yields (avg. 89%, 47 examples). The synthetic potential of this transformation in the late-stage modification of complex natural carboxylic acids and simple modification of the products to three-carbon synthons with ample opportunity for further diversification were demonstrated. DFT studies revealed that the reaction occurs in a stepwise manner through the intermediacy of a conjugated iminium species, which is rapidly captured by the carboxylate ion, resulting in the observed linear selectivity.

《Highly Chemoselective Esterification from O-Aminoallylation of Carboxylic Acids: Metal- and Reagent-Free Hydrocarboxylation of Allenamides》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)Electric Literature of C11H21BrO2.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Simple exploration of 2834-05-1

《Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)SDS of cas: 2834-05-1.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 11-Bromoundecanoic acid(SMILESS: O=C(O)CCCCCCCCCCBr,cas:2834-05-1) is researched.Recommanded Product: 580-34-7. The article 《Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes》 in relation to this compound, is published in Catalysis Science & Technology. Let’s take a look at the latest research on this compound (cas:2834-05-1).

A series of Rh- and Ir-hybrid catalysts with varying tether lengths has been prepared by immobilization of RhI, RhIII and IrIII complexes on carbon black via radical grafting. The performance of the different catalysts was assessed for the hydrosilylation of phenylacetylene with Et3SiH. The efficiency of the catalysts was dependent on the length of the tethers to the surface. The RhIII- and IrIII hybrids afforded the β(Z)-vinylsilanes, as observed for the analogous homogeneous RhIII catalyst. No distinct product selectivity was observed when using the homogeneous RhI precursors as catalysts. However, on using the RhIII hybrid catalysts derived from the RhI precursors to promote hydrosilylation, the major products were the α-vinylsilanes and the origin of the difference in reactivity was found to be a chem. modification of the catalysts during immobilization. Substrate scope is demonstrated for a number of alkynes, and feasible mechanisms supported by DFT calculations are proposed.

《Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)SDS of cas: 2834-05-1.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

The important role of 2834-05-1

Different reactions of this compound(11-Bromoundecanoic acid)Reference of 11-Bromoundecanoic acid require different conditions, so the reaction conditions are very important.

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 11-Bromoundecanoic acid, is researched, Molecular C11H21BrO2, CAS is 2834-05-1, about Adsorption of phenylalanine-rich sequence-defined oligomers onto Kevlar fibers for fiber-reinforced polyolefin composite materials.Reference of 11-Bromoundecanoic acid.

Oligomers comprising four or sixteen phenylalanine residues with regularly intercalated aliphatic chains of different lengths prepared by solid-phase synthesis exhibit sufficient thermal stability to be used as interfacial agents and processed for the preparation of poly(propylene-co-ethylene)-based composite materials. The investigation of their adsorption on Kevlar fibers by SEM is difficult due to the surface heterogeneity of the bare Kevlar fibers. However, oligomers with four successive phenylalanine residues have been clearly observed suggesting their better adsorption on the fiber. The quantification of those oligomers adsorbed on the fibers performed gravimetrically on pellets of fibers has however revealed no significant impact of the length of the aliphatic chain.

Different reactions of this compound(11-Bromoundecanoic acid)Reference of 11-Bromoundecanoic acid require different conditions, so the reaction conditions are very important.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Some scientific research about 2834-05-1

Different reactions of this compound(11-Bromoundecanoic acid)SDS of cas: 2834-05-1 require different conditions, so the reaction conditions are very important.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 11-Bromoundecanoic acid(SMILESS: O=C(O)CCCCCCCCCCBr,cas:2834-05-1) is researched.Application In Synthesis of Basic copper carbonate. The article 《Shaping Liquid Crystals with Gold Nanoparticles: Helical Assemblies with Tunable and Hierarchical Structures Via Thin-Film Cooperative Interactions》 in relation to this compound, is published in Advanced Materials (Weinheim, Germany). Let’s take a look at the latest research on this compound (cas:2834-05-1).

The availability of helical assemblies of plasmonic nanoparticles with precisely controlled and tunable structures can play a key role in the future development of chiral plasmonics and metamaterials. Here, a strategy to efficiently yield helical structures based on the cooperative interactions of liquid crystals and gold nanoparticles in thin films is developed. These nanocomposites exhibit exceptional long-range hierarchical order across length scales, which results from the growth mechanism of nanoparticle-coated twisted nanoribbons and their ability to form organized bundles. The helical assembly formation is governed by the presence of rationally functionalized nanoparticles. Importantly, the thickness of the achieved nanocomposites can be reversibly reconfigured owing to the polymorphic nature of the liquid crystal. The versatility of the proposed approach is demonstrated by preparing helixes assembled from nanoparticles of different geometries and dimensions (spherical and rod-like). The described strategy may become an enabling technol. for structuring nanoparticle assemblies with high precision and fabricating optically active materials.

Different reactions of this compound(11-Bromoundecanoic acid)SDS of cas: 2834-05-1 require different conditions, so the reaction conditions are very important.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Chemistry Milestones Of 2834-05-1

《Syzygium aromaticum (clove) essential oil: An alternative for the sanitization of citrus fruit in packinghouses》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)Application of 2834-05-1.

Application of 2834-05-1. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: 11-Bromoundecanoic acid, is researched, Molecular C11H21BrO2, CAS is 2834-05-1, about Syzygium aromaticum (clove) essential oil: An alternative for the sanitization of citrus fruit in packinghouses.

Citrus canker is a quarentenary disease caused by Xanthomonas citri subsp. citri (X. citri). Thus, sanitization of fresh fruit is a necessary measure before any com. activity. Therefore, we evaluated the clove essential oil (CEO), as an alternative sanitizer for the disinfection of citrus fruit in packinghouses. Tests in vitro and in vivo were carried out to determine the cell inhibitory concentration and to verify the efficacy of the oil for the disinfection of citrus fruits. In in vitro tests, CEO was able to inhibit X. citri when used at 0.75% (volume/volume). In experiments that simulate the sanitization process used in packinghouses, 5% CEO was as effective as the recommended sanitization product based on sodium hypochlorite. GC-MS results showed a high presence of eugenol derivatives as the major compounds of CEO. All results proved that CEO is a potential sanitizer that could be used as an alternative to sodium hypochlorite. Novelty impact statement : Exptl. evidence shows that the clove essential oil (CEO) has the same sanitization efficacy as sodium hypochlorite, which makes of CEO an alternative sanitizer for the decontamination of citrus fruits to be exported to the European Union. CEO is a safer and more sustainable sanitizer for the postharvest disinfection of citrus fruit.

《Syzygium aromaticum (clove) essential oil: An alternative for the sanitization of citrus fruit in packinghouses》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(11-Bromoundecanoic acid)Application of 2834-05-1.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI