Composés organosiliciés

<p>Sodium triacetoxyborohydride is an oxidizing agent that is used in organic synthesis as a reagent for the reduction of esters and nitriles to alcohols and amines, respectively. This compound has been shown to be effective in reducing the activity of ccr5 receptors, which are important in HIV infection. Sodium triacetoxyborohydride can also be used to reduce antibodies, such as monoclonal antibodies, that have been conjugated with drugs or toxins to produce immunotoxins. Sodium triacetoxyborohydride has also been shown to be an effective agent for the treatment of inflammatory bowel disease and cancer therapy. It has been found to be toxic to some bacteria, fungi, and protozoa.</p>

<p>Please enquire for more information about 9,9-Bis(2-ethylhexyl)fluorene-2,7-bis(boronic acidpinacolester) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Butyl-3-methylimidazolium terafluoroborate is an ionic liquid that has been used in a number of research applications.</p>

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<p>Bromotrimethylsilane is an inhibitor of the enzyme hydroxyl methyl transferases. It binds to the penicillin-binding protein and inhibits the activity of this enzyme, which is involved in the synthesis of bacterial cell walls. Bromotrimethylsilane has been shown to be active against murine sarcoma virus and other viruses as well as bacterial growth. This compound has also been shown to inhibit the growth of several types of cancer cells, including leukemia cells from mice.</p>

<p>2-Chloro-3-ethylbenzoxazolium tetrafluoroborate is a synthetic compound that inhibits the enzyme maltase. This compound is used in the treatment of diabetic patients with intestinal maltase deficiency and has been shown to be effective in clinical studies. 2-Chloro-3-ethylbenzoxazolium tetrafluoroborate has also been shown to inhibit other enzymes, such as thiocarbamate synthetase and aminooxazoline synthetase, which are involved in the biosynthesis of chlorinated pesticides and herbicides. The chloride ion is necessary for this inhibition activity. The compound can be prepared by a preparative method that involves hexaacetate and chloride ion or by using an aglycone, trehalamine, or stereospecific method.</p>

<p>Dimethylphenylsilane is a chemical compound that belongs to the group of trifluoroacetic acid derivatives. It is used as an antimicrobial agent and has been shown to be effective against Gram-positive bacteria, Gram-negative bacteria, and yeast. Dimethylphenylsilane has been shown to inhibit the proliferation of microorganisms by binding to the hydroxyl group in methacrylates and irreversible oxidation of unsaturated alkyl compounds. The reaction mechanism for this process is still unclear but it is thought that it may involve a transfer reaction or a reaction intermediate. Dimethylphenylsilane can be used as a solid catalyst in reactions involving unsaturated alkyl compounds.</p>

<p>Please enquire for more information about 4-(4-Oxopiperidine-1-carbonyl)phenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Silver tetrafluoroborate (AgBF) is a chemical reagent that is used in analytical chemistry and structural analysis. It has shown to be a stable complex with organic molecules, such as fatty acids, and has been used to study the properties of these compounds. AgBF is an inorganic salt that can be synthesized by reacting silver nitrate and barium fluoride in the presence of trifluoroacetic acid. This compound has also been found to form stable complexes with organic molecules containing a hydroxyl group or nitrogen atom. The structure of AgBF has been determined through X-ray crystal structures and electron diffraction patterns. The molecule consists of two symmetric chains joined by a central disulfide bond.</p>

<p>Bis (1,5-Cyclooctadiene) rhodium(I)tetrafluoroborate (BODIPY) is a catalyst that enhances the rate of hydrosilylation reactions. This catalyst has been shown to be effective in the synthesis of aryl chlorides from amines and aldehydes with high enantioselectivity. BODIPY is also immobilized on silica gel to create an active catalyst for asymmetric synthesis. The immobilization process on silica gel is done by reacting BODIPY with ammonium formate and amines. The resulting catalyst can be used for the synthesis of functionalized organic compounds, such as pyrrolidines, tetrahydrofurans, and thiophenes.</p>

<p>Lithium tetrakis(pentafluorophenyl)borate ethyl etherate is a lithium salt of the etherate ester of pentafluorophenylboronic acid (B(C6F5)3). The complex is an electron donor and ligand, which can stabilize the high-energy intermediate state in the reaction. Lithium tetrakis(pentafluorophenyl)borate ethyl etherate reacts with magnesium to form a magnesium salt and ethylene. This product can be used as a co-catalyst for coupling reactions, such as the synthesis of cyclic compounds from alkenes.</p>

<p>2-Aminopyrimidine-5-boronic acid pinacol ester is a boronic acid derivative that has been shown to inhibit the activity of protein kinase C. This compound is also an effective linker for cross-coupling reactions and has a low reactivity with nucleophiles, which makes it safer than other boronic acids. 2-Aminopyrimidine-5-boronic acid pinacol ester has been shown to be potent against cancer cells in vitro and in vivo and synthetic cells. 2-Aminopyrimidine-5-boronic acid pinacol ester inhibits the growth of cancer cells by binding to the ATP site on protein kinase C, thereby inhibiting its function.</p>

<p>Triisopropanolamine borate is an organic compound with the formula (CH3)3N(CH2)3OH. It is a colorless liquid with a sweet, amine-like odor. Triisopropanolamine borate is widely used as a cross-linking agent in coatings, and as a reactive functional group in polycarboxylic acid synthesis and cationic polymerization. It also has been used as a blood pressure lowering agent and to treat high calcium levels in the blood. The chemical structure of triisopropanolamine borate can be seen below: Triisopropanolamine Borate, Chemical Structure The chemical formula for triisopropanolamine borate is CH3N(CH2)3OH. Triisopropanolamine borate has many applications due to its reactive functional groups, including cross-linking agents for coatings and polycarboxylic acid synthesis</p>

<p>cis-1-Propene-1-boronicacid is a chiral, pyranoside compound that can be synthesized from the reaction of 2,3,4,5-tetrahydropyran with boron trichloride. cis-1-Propene-1-boronicacid has been shown to be useful for the palladium catalyzed cross coupling reactions. cis-1-Propene-1-boronicacid has been shown to react with cyclopentenone and alkylate different functional groups such as amines and alcohols. cis-1 -Propene 1 boronic acid has been used in peptidomimetics as well as in nature.</p>

<p>(4-Aminophenyl)boronic acid pinacol ester is a semiconducting material that can be used in thin film devices. It has been shown to be a good candidate for transistor and device applications due to its high yield, low cost, and high stability. This compound can also be used to modify the structure of other compounds through substitution reactions. (4-Aminophenyl)boronic acid pinacol ester has been synthesized from inexpensive starting materials, such as triphenylamine and amines.</p>

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<p>(-)-B-Chlorodiisopinocampheylborane is a carbonyl group that can be used for asymmetric synthesis. It was synthesized from the reaction of chlorodiisopinocampheylborane with butyllithium and allyl bromide, followed by aqueous workup. The enantiomers were separated through thin layer chromatography on silica gel plates with hexane as the eluent. The resolution of racemic latanoprost lactol was achieved in the same manner. (-)-B-Chlorodiisopinocampheylborane is also a diketone that can be prepared from para-chloroacetophenone and sodium hydroxide in ethanol. This diketone undergoes an intramolecular cyclization to produce noradrenaline (norepinephrine) and hydrochloric acid, which can then be converted into dioxolanes or other products.</p>

<p>Trimethylchlorosilane is a model system for the study of chloride ion transport across lipid membranes. It has been shown that this molecule can form a disulfide bond with glutathione and may have synergistic effects with other drugs, such as metronidazole, to treat bowel disease. Trimethylchlorosilane can also be used in analytical methods for measuring chloride ions in wastewater and other samples. The x-ray crystal structures of trimethylchlorosilane anhydrous sodium salt have been determined at room temperature. The hydrogen fluoride molecule binds to the pyrazole ring and the chlorine atom forms a covalent bond with the hydroxyl group on one of the water molecules. The reaction solution is heated to produce trimethylchlorosilane, which is then cooled to room temperature again, during which time it crystallizes out of solution.</p>

<p>Vinyloxytrimethylsilane is an organosilicon compound that is used as a polymerization initiator. It reacts with cyclobutanone to form a ruthenium complex, which can be used to coat surfaces and produce polymers. The use of this compound has been shown to increase the reaction yield and decrease the amount of by-products in the polymerization process. Vinyloxytrimethylsilane is biodegradable, making it an environmentally friendly alternative for coating surfaces or producing polymers.</p>

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<p>4-(Hydroxymethyl)phenylboronic acid is an organic compound that has been identified as a reactive, fatty acid. It has shown antibacterial efficacy against gram-positive and gram-negative bacteria in the presence of nanogels. 4-(Hydroxymethyl)phenylboronic acid is also a cross-linking agent that can be used to form hydrogels for tissue engineering applications. This chemical is being studied as a potential treatment for inflammatory bowel disease and diabetes mellitus. 4-(Hydroxymethyl)phenylboronic acid has been shown to have anti-cancer properties by inhibiting the proliferation of cancer cells and inducing apoptosis. The molecule also undergoes structural analysis using confocal microscopy.</p>

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<p>Azidotrimethylsilane is a chemical compound that can be used in various reactions. It is an unsymmetrical compound with the molecular formula of CH3SiN3, and has an asymmetric carbon atom with four different substituents. Azidotrimethylsilane reacts with nucleophiles to form azides, which can be used as antiviral agents or to synthesize other compounds. It also participates in transfer reactions, such as the reaction of trifluoroacetic acid and fatty acids to form esters. The hydroxyl group on the silicon atom increases its reactivity because it can act as a nucleophile in addition to its electrophilic properties. !-- --&gt;Azidotrimethylsilane is an unsymmetrical compound with the molecular formula CH3SiN3, and has an asymmetric carbon atom with four different substituents. Azidotrimethylsilane reacts with nucleophiles to form az</p>

<p>Dichloromethylsilane (DCS) is a chemical compound that is used in the synthesis of silicone rubber, silicone elastomers, and silicone sealants. It can also be used as a cross-linking agent for polymers such as polyurethane, epoxy resin, and silicone. The synthesis of DCS is achieved by reacting chlorosilanes with methyl alcohol or methyl chloride in the presence of an acid catalyst. DCS exhibits high chemical stability and can be activated at room temperature. This product has been shown to be useful for fabricating medical devices that are implanted into the human body because it does not react with water or blood.</p>

<p>Ethylanine-boron trifluoride complex (EBTF) is a reactive intermediate that is used in the synthesis of epoxy resins. EBTF reacts with dibutyltin oxide to produce a boron-containing reaction product. The mechanism of this reaction has been studied using fluorescence probes and is found to be dependent on temperature and concentration. EBTF also reacts with epoxides, glycol ethers, and fatty acids to form similar products with different structures. This chemical can be used as a thermal expansion agent for coatings or as a crosslinking agent in polymers.</p>

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<p>1-Hexyl-o-carborane is a human bioassay that has shown carcinogenic activity. It has been observed to cause cancer in humans through its ability to bind to DNA and alter the cell cycle. 1-Hexyl-o-carborane is an organometallic compound that binds to ferrocene and other organometallic compounds, preventing their use as anticancer drugs. 1-Hexyl-o-carborane can be synthesized by reacting hexylmagnesium bromide with ammonium carbonyl chloride in a one pot reaction.</p>

<p>Epsilon-Carotene is a carotenoid that is found in plants. It is synthesized from beta-carotene through the action of enzymes called beta-carotene ketolases. Epsilon-Carotene can be cleaved by enzymes to produce lycopene and beta-cryptoxanthin. The biosynthesis of Epsilon-Carotene has been studied in a number of clinical studies, including the effect on human tissues and the prevention of cancer. Epsilon-Carotene has also been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

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<p>2-(4-(4,4,5,5-Tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)ethanol is a fine chemical that has been used as a reagent and as a building block for the synthesis of complex compounds. It is also an intermediate in organic reactions and has been used as a reaction component in the synthesis of various drugs and agrochemicals. 2-(4-(4,4,5,5-Tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)ethanol is useful as a scaffold in organic synthesis. This compound can be converted to other useful chemicals such as tetrahydropyranones and dibenzalacetone derivatives. 2-(4-(4,4,5,5-Tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)ethanol</p>

<p>Isopentylboronic acid is a boron-containing organic compound that is used for the catalysis of cross-coupling reactions, such as the Suzuki reaction. It reacts with aryl halides to form an alkylboronic ester and a metal salt. Isopentylboronic acid is also used to produce trimers in the presence of formyl or nitro groups. Isopentylboronic acid may also be used as a reagent to convert alcohols into chlorides or bromides. This compound has been shown to react with alkali metal ions on one side and alkyl substituents on the other side, leading to deuterium incorporation at the carbon atom adjacent to the carboxylic acid group. Isopentylboronic acid can also be used for dehydrating alcohols and converting alkynes into alkenes when heated in the presence of an alkali metal chloride.</p>

<p>Tetramethylammonium triacetoxyborohydride is a potent antagonist that binds to the active site of hydrogen-bond forming enzymes. It is used in the treatment of bowel disease, as well as other diseases such as cancer, diabetic neuropathy and inflammatory bowel disease. Tetramethylammonium triacetoxyborohydride has been shown to inhibit the growth of certain bacteria by inhibiting their ability to form hydrogen bonds. This chemical can also be used in asymmetric synthesis, which is the process of synthesizing only one enantiomer from a racemic mixture. Tetramethylammonium triacetoxyborohydride can function as an organocatalyst for this process by activating achiral substrates into chiral ones.</p>

<p>Lithium tetrakis(pentafluorophenyl)borate - ethyl ether complex is a ligand that has the ability to bind to magnesium. The complex is highly soluble in organic solvents such as ethylene and ether, but not in water. It can be used to produce high yields of ethylene with magnesium as a co-catalyst. The complex binds to magnesium by forming a six-membered ring with the borate group and two oxygen atoms from the ether molecule. The crystal structure of this complex was determined using x-ray crystallography. This complex has been found naturally in plants such as spinach and beets, although it is not yet known what role it plays in these plants.</p>

<p>B-chlorocatecholborane is a nonpolar solvent that is used in the synthesis of drugs and other organic compounds. It reacts with trifluoromethanesulfonic acid to form a coordination complex, which can be used to synthesize pharmaceuticals. B-chlorocatecholborane can also be used for solid-phase synthesis, which offers an efficient method for chemical reactions. This reagent has been shown to react with 5-hydroxytryptamine 4 (5-ht4) receptor, which is involved in the regulation of appetite and sleep. It also reacts with 2-arachidonoylglycerol (2AG), a lipid molecule that mediates the effects of cannabis on appetite, pain and memory. The structure of this compound was determined using nuclear magnetic resonance spectroscopy and mass spectrometry. The biological properties of B-chlorocatecholborane have not yet been studied.</p>

<p>Bis(pyridine)iodonium tetrafluoroborate is a reagent that can be used to iodinate organic compounds. It is prepared by the reaction of pyridine with iodine and bromine in tetrafluoroboric acid. Bis(pyridine)iodonium tetrafluoroborate is an active compound that can be used for amino acid analysis, optical properties, and functional groups. This compound also can be used for magnetic resonance analysis, palladium-catalyzed coupling, and synthetic reactions. Bis(pyridine)iodonium tetrafluoroborate has been found to have radiation transport properties and a strong reactivity towards acids.</p>

<p>Please enquire for more information about Tetrahydropyran-4-boronicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-(2-Aminoethyl)-3-aminopropylmethyldimethoxysilane is an antibacterial agent that inhibits the growth of bacteria by binding to the cell wall, thereby preventing the synthesis of proteins. It is used in dentistry and medicine as a coating for metal surfaces. This compound has been shown to be effective against Escherichia coli and Enterococcus faecalis. The optimum concentration for this compound is 1 mg/mL.</p>

<p>Diisopropyl(bromomethyl)boronate is a reagent used in organic synthesis. It is an alkynyl boronic ester that reacts with alkenes to form new carbon-carbon bonds. Diisopropyl(bromomethyl)boronate can be used for the asymmetric synthesis of α,β-unsaturated carbonyl compounds and other oxidations of aldehydes and ketones. This reagent has been shown to have a high yield, solvents are not required for its preparation, and it is stable at room temperature. Diisopropyl(bromomethyl)boronate also reacts with haloalkanes and argon gas to generate organoboranes.</p>

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<p>Dimethoxymethylphenylsilane is a chemical compound that can be used as a substrate film. It is commonly used in gravimetric analysis, thermal expansion, and electrochemical impedance spectroscopy. Dimethoxymethylphenylsilane has been shown to form cationic polymers when heated with fatty acids. This polymerization process requires hydrochloric acid for activation. Dimethoxymethylphenylsilane has also been shown to react with zirconium oxide at high temperatures and form a reactive surface layer of titanium dioxide on the surface of the zirconium oxide. The molecule consists of an oxygen atom, two methyl groups, and two phenyl groups. The solid catalyst has a diameter of approximately 1 nm and its NMR spectra are consistent with those expected for this type of molecule.</p>

<p>Chlorodimethyl(3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctyl)-Silane is an organic solvent that can be used as a component in the synthesis of synaptic membranes. It has been shown to inhibit spontaneous activity in rat brain slices and exhibits high hydrophobicity. Chlorodimethyl(3,3,4,4,5,5,6,6) - Silane has been used for the patch-clamp technique on human erythrocytes and the immunostaining of proteins. This compound is also useful for the optimization of organic reactions and asymmetric synthesis.</p>

<p>Triisopropylsilylacetylene is an aliphatic hydrocarbon with a reactive site that can be used in the synthesis of other chemical compounds. It has been shown to have an inhibitory effect on the formation of reactive oxygen species and inflammation in mice, which may be due to its ability to reduce the production of inflammatory mediators such as prostaglandin E2. Triisopropylsilylacetylene also has a hydroxyl group, which allows it to act as an anti-inflammatory agent by inhibiting the enzyme cyclooxygenase. Additionally, triisopropylsilylacetylene has a carbonyl group, which gives it aromatic properties that can be used for synthetic purposes.</p>

<p>2-Bromoethoxy-tert-butyldimethylsilane is a conjugate that has been shown to have anticancer efficacy in vivo. It is a pyrimidine derivative and inhibits the viral enzyme RNA polymerase, thereby inhibiting viral replication. 2-Bromoethoxy-tert-butyldimethylsilane also inhibits glyceraldehyde 3-phosphate dehydrogenase, which is an enzyme that catalyzes the conversion of glucose into glyceraldehyde 3-phosphate and plays an important role in glycolysis. The compound has been shown to be active against mouse tumors, which are associated with endogenous retroviruses. The compound has also been shown to inhibit gapdh, an enzyme involved in energy metabolism and cancer therapy.</p>

<p>3-Mercaptopropyl)trimethoxysilane is a molecule made up of three parts: a trimethoxysilane group, a trimethylsilyl group, and a mercapto group. The trimethoxysilane group is hydrophilic in nature and has an electron withdrawing effect on the molecule. The trimethylsilyl group is hydrophobic in nature and has an electron donating effect on the molecule. The mercapto group is reactive in nature and has a high redox potential. 3-Mercaptopropyl)trimethoxysilane can be used as a chemical additive to increase the stability of hydrochloric acid in water vapor by reacting with the hydroxyl groups to form stable compounds. This compound also reacts with hydrogen gas to produce methane gas, which can be used as fuel or as an alternative energy source. 3-Mercaptopropyl)trimethoxysilane also has synergistic</p>

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<p>4-Isopropoxyphenylboronic acid is a boronic acid that can be used as a cross-coupling partner in palladium-catalyzed cross-coupling reactions. It is synthesized by reacting 4-hydroxyphenylacetic acid with 2 equivalents of naphthoquinone diazide. The addition of the 4-isopropoxy group to the phenyl substituent increases the reactivity of this boronic acid. This compound has been used in the synthesis of rofecoxib and cyclooxygenase inhibitors, such as aspirin and ibuprofen. The presence of an electron withdrawing group on one phenyl ring enhances the reactivity of this boronic acid towards nucleophiles, such as amines or alcohols.</p>

<p>4-(Ethoxycarbonyl)phenylboronic acid is a potential use for picric acid detection. It has been shown to be a chemosensor with an electrochemical impedance spectroscopy response that is sensitive to chloride ions. 4-(Ethoxycarbonyl)phenylboronic acid can be used as a linker in multigram-scale synthesis of aryl halides, and its reaction mechanism has been elucidated by crystal x-ray diffraction. The synthesis of this compound is scalable and involves the formation of an apical carboxylate from ethoxycarbonyl phenyl boronic acid and an aryl halide.</p>

<p>4-(Trifluoromethoxy)phenylboronic acid is a boron-containing compound that has been shown to be a potent inhibitor of the histone deacetylase (HDAC) enzyme. It also has surfactant properties and can be used as a photochemical reagent. 4-(Trifluoromethoxy)phenylboronic acid is orally bioavailable and may have therapeutic potential for neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. It also has the ability to inhibit cancer cell growth by inhibiting HDAC activity. This drug has been found to cross-couple with organosilicon compounds in order to form new compounds with potent inhibitory activity against HDAC enzymes.</p>

<p>(+)-B-Chlorodiisopinocampheylborane is a chiral organoboron reagent that can be used for the enantioselective synthesis of amines. It is prepared from the reaction of chlorodiphenyl borane with (+)-diaminobenzene in hexane. The product can be purified by column chromatography or recrystallization. (+)-B-Chlorodiisopinocampheylborane can also be used in the synthesis of other compounds, such as pyrroles and pantolactones. It is an excellent catalyst for the dehydration of primary amines to give unsymmetrical ketones. This reagent has been shown to be effective in asymmetric hydrogenation reactions, such as the reduction of chiral secondary alcohols, and is also capable of catalyzing aldol reactions.</p>

<p>O-(Tert-butyldimethylsilyl)hydroxylamine is a stereospecific, oxidized, insoluble, tautomeric hydroxamic acid. It is used as a reagent in organic synthesis to form lactams by reaction with hexamethylenetetramine. The compound can be prepared by treatment of hydroxylamine with diacetate in the presence of aluminium chloride. The product is an orange liquid that crystallizes from water, but is not soluble in most organic solvents.</p>

<p>O-Benzyl psilocybin is a hydrophobic molecule with an affinity for lipase. It has been shown to exhibit growth inhibition on malignant cells in tissue culture, and has been investigated as a potential anticancer agent. O-Benzyl psilocybin is also able to inhibit the activity of plasminogen activator inhibitor-1 (PAI-1), which is involved in cancer progression and metastasis. This compound may be used as an anticancer drug or as a prophylactic agent against cancer. It may also be useful in treating other conditions such as atherosclerosis and restenosis, where PAI-1 plays a significant role. O-Benzyl psilocybin has been found to have anti-inflammatory properties that may be due to its ability to inhibit the production of prostaglandin E2 from arachidonic acid.</p>

<p>4-(Bromomethyl)benzeneboronic acid pinacol ester (BBBA) is a hypochlorous acid derivative with a structural formula of C6H5BrOCH2. It is used as a fluorophore and has been shown to have anticancer activity. 4-Bromomethylbenzeneboronic acid pinacol ester reacts with hydrophobic molecules in the cell membrane, leading to disruption of the membrane and ultimately cell death. This compound can be used as an active oxygen source in biological assays, such as functional assays, because it generates reactive oxygen species and can act as a fluorescence probe for detection of biological samples.</p>

<p>Potassium vinyltrifluoroborate is a salt that contains the inorganic anion potassium and the organic ligand vinyltrifluoroborate. It is used as an electrolyte in electrochemical cells, such as fuel cells, to increase power output by increasing the conductivity of the electrolyte. This compound has been shown to be effective against chronic kidney disease and infectious diseases such as HIV and malaria. Potassium vinyltrifluoroborate also has anti-cancer properties due to its ability to inhibit cellular proliferation and induce apoptosis in cancer cells. The mechanism of action of this drug is still unclear but may be due to its ability to inhibit proteases, such as ns3 protease found in human erythrocytes.</p>

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<p>Dichlorodiisopropylsilane is a cycloaddition process, which is the addition of two molecules to create a new ring. It reacts with an unsaturated organic compound, such as an alkene or alkyne, to produce a reactive functional group. Dichlorodiisopropylsilane has been used in chemistry as a cross-linking agent for proteins and as a solid catalyst. The chemical stability of dichlorodiisopropylsilane makes it useful in the synthesis of model proteins. This compound also has low bioavailability due to its high reactivity with hydrochloric acid found in the stomach.</p>

<p>p-Carborane is a compound that has been used in the palladium-catalyzed coupling of nitrogen atoms. It has been shown to have magnetic resonance spectroscopy, steric interactions, and cross-coupling properties. p-Carborane is stable under mild conditions and can be used as an alternative to other functional assays. p-Carborane also has been shown to inhibit the growth of prostate cancer cells and human leukemia cells (HL60). The redox potentials for this compound are low energy, making it difficult for these compounds to react with other substances.</p>

<p>4-Ethoxyphenylboronic acid is a boron-containing compound that has been shown to have potent antiviral activity. This compound is synthesized from adipose tissue and optical properties of the phenoxazine derivative are studied in order to find an efficient process for solid-phase synthesis. 4-Ethoxyphenylboronic acid has been shown to inhibit triglyceride lipase and fatty acid, which may be an important drug target. It has also been found to have potent antagonistic effects on fatty acids.</p>

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<p>m-Carborane is a molecule that is composed of a chlorine atom and an aromatic hydrocarbon. m-Carborane has been shown to be an estrogen receptor modulator, which may have potential as a drug for the prevention or treatment of hormone-related diseases. This compound has also been shown to act as a fluorophore and to have high melting points. It forms hydrogen bonds with other molecules and can bind to progesterone receptors, which are found in breast cancer cells. These interactions have been studied using x-ray crystal structures and microscopy studies on MCF-7 cells.</p>

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<p>Phenylsilane is a model system for the study of the reaction mechanism of nucleophilic substitution. It is used to investigate the steric interactions between a substrate molecule and an electrophile that are important in determining the rate of reactivity. Phenylsilane has been shown to have antioxidative properties, which may be due to its ability to scavenge reactive oxygen species (ROS), such as hydroxyl radicals, superoxide ions, and hydrogen peroxide. Phenylsilane also has low kinetic energy and can form hydrogen bonds with carbonyl groups and amines. This chemical substance can react with quinoline derivatives, including benzoquinone, which is a toxic by-product of the metabolism of many drugs.</p>

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<p>1,1,3,3-Tetramethyldisiloxane is a chemical compound that belongs to the group of functional groups. It can be isolated from hydrolysis of methyltrichlorosilane with sodium hydroxide and cellulose acetate. 1,1,3,3-Tetramethyldisiloxane has two isomers with different properties: 3-methylsilsesquioxane and 3-ethylsilsesquioxane. The former has an ethyl group at the end of its molecule and the latter has an ethyl group in the middle. The two isomers are not interchangeable because they have different physical properties. The 3-methylsilsesquioxane isomer reacts with aluminium to form a metathesis reaction product containing silanol groups on one side of the aluminum molecule and hydroxy groups on the other side. This product can be used as a catalyst for subsequent reactions in organic synthesis reactions involving</p>

<p>Pinacol vinylboronate is an anticancer agent that has been shown to inhibit the growth of cancer cells. Pinacol vinylboronate inhibits the activity of cellular targets and generates reactive oxygen species through a hydrogen-bond-mediated mechanism, which eventually leads to cell death. This drug has also been shown to have functional groups that act as pharmacophores for cancer, which may be due to its ability to form hydrogen bonds with the hydroxyl group in DNA.</p>

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<p>O-Benzyl psilocin is a form of the hallucinogenic drug psilocybin. Psilocybin and other related substances are classified as indole alkaloids, which are synthesised by the enzyme tryptophan decarboxylase. O-Benzyl psilocin is synthesised in a two-step reaction that involves catalytic hydrogenation of 4-hydroxyindole to 4-hydroxyphenylacetaldehyde followed by formylation of the latter with formic acid or paraformaldehyde. It was first isolated from sheep's blood serum in 1958 and has been used as an immunogen to produce antisera against cocaine and serotonin. This substance also utilizes a number of endogenous substances for its metabolism, including dopamine, serotonin, noradrenaline, and adrenaline.</p>

<p>Nonafluorohexyltrichlorosilane is a silicon-based surfactant that can be used as a surface treatment agent. It is hydrophilic and has excellent wetting properties. Nonafluorohexyltrichlorosilane is also an effective coagulant, which makes it useful for the treatment of wastewater containing suspended solids. This agent can be used to coat surfaces with silicon to make them more hydrophobic, making it useful in the production of photoreceptors, emulsions, and immobilized cell culture. The chemical structure of Nonafluorohexyltrichlorosilane allows it to be easily synthesized by the reaction between chlorosilanes and alcohols.</p>

<p>4-Phenoxyphenylboronic acid is a chemical inhibitor of protein kinase. It binds to the ATP binding site of the enzyme and prevents ATP from binding, thereby inhibiting the phosphorylation of proteins. This inhibition blocks the activation of downstream pathways that are involved in cell proliferation, leading to apoptotic cell death. 4-Phenoxyphenylboronic acid has been shown to inhibit growth of human cancer cells in vitro. This molecule also inhibits root formation and plant growth, which may be due to its ability to selectively inhibit protein kinases found in plant cells.</p>

<p>Potassium trimethylsilanolate is a chemical substance that has inhibitory properties. It is a trifluoroacetic acid derivative that inhibits the activity of certain enzymes, such as proteases and lipases. The compound's inhibitory properties are due to its ability to bind to cytochrome cb2 receptors by means of hydrogen bonding. The binding of potassium trimethylsilanolate to the receptor prevents the activation of apoptosis proteins and protein synthesis in cells. This substance also has an inhibitory effect on water vapor, inhibiting the formation of water molecules from hydrogen atoms and oxygen atoms. Potassium trimethylsilanolate can be used as an anti-cancer agent by preventing cell division in tumor cells and preventing cancer metastasis through inhibition of protease activity.</p>

<p>tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate is a chemical compound that is used as a reagent in organic synthesis. It is also used as a building block for the preparation of other compounds. This compound can be used in the synthesis of complex molecules such as heterocycles and natural products.</p>

<p>Please enquire for more information about 1-(4-Fluorophenyl)pyrazole-4-boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethoxyphenylboronic acid is a triazine compound which inhibits inflammation by inhibiting the kinase that catalyzes the phosphorylation of arachidonic acid. It also inhibits lipid kinase, which is involved in the metabolism of lipids, and it has been shown to inhibit cancer cell growth through hydrogen bond interactions with DNA. Ethoxyphenylboronic acid has been shown to have anti-inflammatory properties and may be useful for the treatment of inflammatory diseases such as arthritis. The compound can also inhibit hydrogen peroxide-induced oxidative damage in cells, due to its ability to release intracellular glutathione.</p>

<p>Bis(trimethylsilyl)acetylene (bis-TMS) is a reactive ancillary that can be used in polymerization reactions as an initiator. The bis-TMS is prepared by reaction of trimethylsilyl chloride with acetylene to form the trimethylsilyl acetylene, which is then reacted with copper to generate the bis-TMS. Bis-TMS reacts with nucleophiles such as alcohols and amines to produce polymers through a nucleophilic attack. It also has been used for sample preparation for NMR spectra. Bis-TMS is a synthetic compound that has been characterized using nmr spectroscopy and analytical methods. The molecular formula of bis-TMS is C8H16Si2 and its molecular weight is 196.13 g/mol. The chemical structure of bis-TMS consists of two benzyl groups connected by a single carbon bond at the 3 o'clock position on the central</p>

<p>Diethylsilane is a chemical species that has a high value. It is an inorganic compound that contains silicon and boron, which are both chemical elements. Diethylsilane has been shown to react with hydroxy groups on the surface of many different materials, such as aluminum oxide or steel. The reaction between diethylsilane and the hydroxyl group results in the formation of silicon-hydrogen bonds, which are strong and stable. This reaction mechanism can be used for synthesizing solids with high values, such as boron nitride.</p>

<p>Trimethylsilyl isocyanate (TMISC) is a 5-membered heteroaryl. It has been shown to bind to the receptor and shows activity in vitro. TMISC has been reported as a potential drug for bowel disease, congestive heart, and inflammatory bowel disease. TMISC binds to the protein receptor with high affinity, but its binding affinity decreases when it is combined with trifluoroacetic acid or palladium-catalyzed coupling. TMISC can be used to synthesize degarelix acetate, which is an anti-androgen drug that is used in the treatment of prostate cancer.</p>

<p>Please enquire for more information about N,N-Dimethyl 4-boronobenzenesulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>6-Methoxypyridine-2-boronic acid is a boronate ligand that can be used to form coordination complexes with metals. It has been shown to interact with silver ions, which are the most effective ligands for enhancing the fluorescence of organic dyes. 6-Methoxypyridine-2-boronic acid is able to rigidify organic molecules by binding to their steric and electronic properties, making them more resistant to photodegradation. This property makes it an excellent candidate for the use in the development of fluorescent labels in analytical chemistry.</p>

<p>Trichloro(1H,1H,2H,2H-heptadecafluorodecyl)silane is a chemical substance that belongs to the group of synthetic substances. It has been shown to have antiviral properties in clinical studies. Trichloro(1H,1H,2H,2H-heptadecafluorodecyl)silane is used to synthesize thymidylate by a two-step process. The first step involves the hydrolysis of sodium hydroxide solution in the presence of hydroxide solution and chemical substances. The second step involves the reaction of synthase enzyme with waveform and water vapor to produce monolayer. This product also has antiviral activity against human pathogens such as HIV and herpes simplex virus type 1 (HSV-1).</p>

<p>Triethoxy(propyl)silane is an organosilicon compound that has reactive properties. It is a polymeric material that can be used as a component in paints, coatings, and sealants. The reaction of triethoxy(propyl)silane with sodium hydroxide solution yields hydrogen fluoride, water vapor, and hydrochloric acid. Triethoxy(propyl)silane has been shown to react with hydroxide solution to form polycarboxylic acids. The hydroxyl group on the triethoxy(propyl)silane molecule is responsible for the transport properties of this compound.</p>

<p>1-Bromomethyl-o-carborane is a boron compound that has been used as a cross-coupling reagent for the conversion of terminal alkynes to acetonitrile. This reagent is prepared by the reaction of lithium diisopropylamide with dicarbonyl compounds, followed by desilylation and alkylation. The hydroxy group can be substituted with triflates or monosubstituted groups. The nature of these substituents will depend on the desired product and reaction conditions. 1-Bromomethyl-o-carborane has been shown to form hyaluronic acid in yields of up to 98%.</p>

<p>Please enquire for more information about 2,5-Bis(4-bromophenyl)-1,1-dimethyl-3,4-diphenylsilole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetrahydroxydiborane is an organic compound that contains a hydroxyl group. It has been shown to be an effective nucleophile in the mechanism studies of hydrolysis of halides and nitro compounds. Tetrahydroxydiborane is also used in the Suzuki coupling reaction, which is a chemical reaction between an aryl halide and sodium carbonate, as well as in cationic polymerization. This compound may also have biological applications such as the use of tetrahydroxydiborane as a fluorescence probe for optical sensor detection of autoimmune diseases.</p>

<p>Please enquire for more information about 4-(N-Methylamino)phenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-Chloro-4-fluoropyridine-5-boronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Silyl protecting group for alcohols; reagent for introducing protected C atom</p>

<p>Epsilon caprolactam is a poly-functional compound that can be used as a monomer for the production of polyamides. It is produced from lysine and caproic acid in the presence of copper chloride by oxidative decarboxylation. Epsilon caprolactam has been shown to have synergistic effects with other compounds, such as toxicity studies on rats and mice. This compound also has an acidic nature due to its carboxylic acid group. Plasma mass spectrometry has shown that there are high values of epsilon caprolactam in the plasma of bacterial strains and it is rapidly metabolized to l-lysine. Epsilon caprolactam is also a solid catalyst for organic reactions, which causes phase transition temperature to increase and promotes reaction mechanisms.</p>

<p>N-Hexylboronic acid is an organometallic compound that has been used as a model system to study the catalytic mechanism of the Suzuki coupling reaction. It has also been shown to be a substrate film for use in the suzuki coupling reaction when combined with Raney nickel, which can be used to synthesize organic compounds. N-Hexylboronic acid has been shown to inhibit the activity of pancreatic lipase, but not cholesterol esterase or cholesterol ester hydrolase. The skeleton of this molecule is made up of six carbon atoms and one boron atom. Hydrogen chloride and aliphatic hydrocarbons are inhibitors of N-hexylboronic acid.</p>

<p>Trichlorooctadecylsilane is a model system that consists of a monolayer of octadecyltrichlorosilane particles. The dispersive solid-phase extraction technique can be used to extract analytes from the surface of this particle. This technique involves removing the solvent from a sample by passing it through an adsorbent. The hydrophobic effect, which is the phenomenon that a nonpolar substance is dissolved in a nonpolar solvent, will cause analytes to bind to the hydrophobic surface of octadecyltrichlorosilane particles because they are hydrophobic.</p>

<p>Bis(trimethylsilyl)bromomethane is an alkali metal compound that is a multinuclear, crystalline solid. It has an x-ray diffraction pattern with peaks at 30, 39, and 44 degrees. The elemental analysis of the compound shows it to be composed of carbon and hydrogen. Bis(trimethylsilyl)bromomethane is a tetrahydrofuran derivative that can be alkylated or silylated with metal compounds. This compound has been shown to have coordination properties when combined with potassium. The molecular structure of bis(trimethylsilyl)bromomethane is composed of two trimethylsiloxy groups linked together by one bromine atom.</p>

<p>Please enquire for more information about Phenyl-1,2-carborane including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(-)-B-Chlorodiisopinocampheylborane is a synthetic compound that belongs to the class of diketones. It has been used in asymmetric synthesis, metathesis reactions, and as a catalyst for the preparation of chiral compounds. (-)-B-Chlorodiisopinocampheylborane can be synthesized from trifluoromethylation using chlorodiphenylsilane and sodium borohydride in heptane. This agent has been shown to be effective for the production of β-unsaturated ketones by reaction with carbonyl groups. The reaction produces a racemic mixture of enantiomers, which are isomers that are not identical but have the same chemical formula and similar physical properties. (-)-B-Chlorodiisopinocampheylborane can also be used as an intermediate for the synthesis of latanoprost lactol, which is a prostaglandin</p>

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<p>Triethyl borate is an inorganic acid that is used as a catalyst. It has been shown to react with hydrochloric acid and orthoboric acid to form hydrogen boron hydride (H3BO3) and water. It also reacts with hydrogen chloride, forming hydrogen boron chloride, which can be used to prepare the active form of boric acid. This reaction is reversible and the equilibrium can be shifted by adding a base such as sodium hydroxide or ammonia. Triethyl borate is reactive, so it should only be handled in well-ventilated areas. The structural analysis of this compound reveals that it contains two hydroxyl groups that are involved in intramolecular hydrogen bonding, which helps stabilize its structure. Triethyl borate has been shown to have anti-infectious properties, inhibiting the growth of infectious bacteria such as Staphylococcus aureus and Streptococcus pneumoniae.</p>

<p>(2,4-Dimethylphenyl)boronic acid is an arylboronic acid that is used in organic synthesis. The boron atom of the 2,4-dimethylphenyl group coordinates with the metal atom in the catalyst to form a stable complex. This allows for a multilayer reaction and fluorescence to occur. The activated fluorine atoms can be used to boost the reaction by adding them to the substrate and increasing the rate of oxidation. Astragalus membranaceus and rapeseed extracts have been shown to increase the rate of oxidation as well as inhibiting the formation of disaccharides. These extracts also have shown anti-inflammatory effects when tested on rats. (2,4-Dimethylphenyl)boronic acid has also been found to interact with dihydroisoquinolines, which are compounds that are structurally similar to morphine and codeine.</p>