Organosilicon Compounds

Please enquire for more information about 2-Methyl-6-isobutoxypyridine-3-boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about B-[3-[[2-Hydroxy-3-[3-(triethoxysilyl)propoxy]propyl]amino]phenyl]boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6-(Dimethoxymethyl)pyridin-2-ylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

S12400 - Octamethylcyclotetrasiloxane

Please enquire for more information about 6-Methoxyindole-2-boronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

High performance small molecule for OFET applications

S19625 - Trimethylsilyl methacrylate inhibited MEHQ

S11825 - Methyltrimethoxysilane

Please enquire for more information about 5-Acetyl-2-fluorophenylboronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

S15875 - Tetrakis(trimethylsiloxy)titanium

6-Ethoxy-2-naphthaleneboronic acid is a biphenyl that can be synthesized by the cross-coupling of 6-ethoxy-2-naphthol and boronic acid. The compound is a reactive, apical ligand that has been used in organometallic chemistry. It is also a hydrophobic, polyhedra ligand. 6-Ethoxy-2-naphthaleneboronic acid has been shown to have nature, advances, and inorganic properties due to its use as a ligand for metal ions in inorganic base reactions. Crystal x-ray diffraction has shown that the compound has a crystal structure with an orthorhombic symmetry. This compound was first synthesized in 1985 by researchers at the University of Michigan.br>br> The synthesis of this compound involves the reaction between trimethylsilylacetylene and 4-(6'-ethoxynaphthyl)

Please enquire for more information about N,N-Diethyl 3-boronobenzenesulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-Acetoxy-1-propenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

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S25283 - Triisopropoxysilane,95%

Please enquire for more information about 3-(Ethylsulfonamido)phenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Triphenylsilanol is a model system for the study of damaged solid catalysts. It has been shown to be thermally stable and can be used as a catalyst in organic reactions. Triphenylsilanol has an hydroxyl group, which allows it to undergo hydrolysis by hydrochloric acid. FT-IR spectroscopy has been used to determine the structure of triphenylsilanol, which is a cationic polymerization catalyst that forms hydrogen bonds with other molecules. Triphenylsilanol also forms intermolecular hydrogen bonds with magnesium salts and x-ray crystal structures have been determined.

Bis(trimethylsilyl)carbodiimide (BTSC) is a carbodiimide that has been used extensively in the chemical industry as a reagent for the synthesis of urea- and thiourea-containing polymers. It is also used to prepare immobilized dyes and fluorescent probes, to coat surfaces, and to catalyze chemical reactions. BTSC reacts with hydrogen fluoride (HF) at room temperature by forming hydrogen gas and bis(trimethylsilyl)urea, which can be quantified using gravimetric analysis. Bis(trimethylsilyl)carbodiimide reacts rapidly with chlorine gas (Cl2), yielding dichlorocarbene, which can be quantified using luminescence properties. The reaction of BTSC with silicon dioxide (SiO2) yields Si-N bonds that are useful in coating applications. Bis(trimethylsilyl)carbodiim

3-Chloro-4-fluorophenyl)boronic acid (3CFPBA) is a boronic acid that is used in asymmetric synthesis. It has high lipophilicity and can be taken up by the brain. 3CFPBA has been shown to bind to naphthalene, which is a natural compound, with a binding constant of 2.6 x 10^10 M^-1. This molecule has been found to inhibit the production of beta amyloid peptides in Alzheimer's disease . 3CFPBA also binds to other heterocycles such as furan and pyrrole, which are found in molecules such as phenol and benzene respectively.

Please enquire for more information about 3-Hydroxymethyl-4-methylphenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Dimethoxydimethylsilane is a chemical compound that is synthesized by the reaction of sodium carbonate and magnesium chloride. It has high values for particle size, light signal, thermal expansion, and light emission. Dimethoxydimethylsilane has been shown to react with water vapor to produce hydrogen gas and oxygen gas. This reaction mechanism is similar to the Haber-Bosch process used in industrialization of ammonia production. The hydroxyl group on dimethoxydimethylsilane can be cleaved by human serum, which may lead to an adverse effect on human health.

(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.

Please enquire for more information about 2-Methoxyphenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-(1H-Pyrazol-1-ylsulfonyl)phenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Methyl-1H-pyrazole-5-boronic acid pinacol ester is a reagent that is used in the synthesis of organic compounds. It can be used to synthesize an inorganic base, such as chloride, and is also used in the synthesis of chlorobenzene derivatives. 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester has been shown to react with suzuki coupling reactions and acylation reactions. This compound can also be used for the synthesis of malonate, which is a stable isotope that can be used for cancer research or other innovative applications. 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester reacts with iodomethane to form naphthalene derivatives, which are reductive amination products.

Please enquire for more information about 3-Fluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (3R,4S)-1-Benzoyl-4-phenyl-3-[(triethylsilyl)oxy]-2-azetidinone including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Fluoro-6-hydroxyphenylboronic acid is an organic compound that is used in the synthesis of pharmaceutical compounds. It is a white solid that can be obtained as a byproduct during the preparation of 3-fluorophenol. 2-Fluoro-6-hydroxyphenylboronic acid can be used as a catalyst in reactions involving trimethyl borate, butyl lithium, and hydrolysis reactions. This compound has been shown to catalyze the reaction of butyl lithium with acids such as sulfuric acid and phosphoric acid. The use of this compound in catalysis may lead to the production of pharmaceutical compounds.

Mesitylboronic acid is a divalent organoboron compound with the molecular formula CHB(O)OH. It is a white solid that is soluble in organic solvents, but not water. Mesitylboronic acid has been used for the palladium-catalyzed cross-coupling of aryl halides and vinylogous esters, yielding substituted pyridines. Mesitylboronic acid also catalyzes the Suzuki coupling reaction of aryl boronic acids and alkenes, producing substituted indoles. This compound has diagnostic applications due to its ability to form a fluorescent complex with certain metal ions. It also plays an important role in insulin resistance due to its ability to form cross-couplings with unsymmetrical boron compounds.

Please enquire for more information about [4-(Pyrrolidine-1-carbonyl)phenyl]boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-alpha-Fmoc-Nepsilon-2,4-dinitrophenyl-L-lysine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Methyl(R)-(+)-3-(tert-butyldimethylsilyloxy)-5-oxo-1-cyclopentene-1-heptanoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (2,6-difluoro-4-methoxyphenyl)boronic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Cyanopyridine-5-boronic acid pinacol ester is a reagent in organic synthesis. The synthesizing process is based on the reaction of boron trioxide with 3-cyanopyridine and pinacol. This reagent is used as a starting material to produce other chemicals, such as pharmaceuticals, dyes, and pesticides. It can also be used to prepare Grignard reagents for reactions with alcohols or phenols. 3-Cyanopyridine-5-boronic acid pinacol ester is an industrial chemical that is mainly used in the manufacturing of polyurethanes, acrylic fibers, and plastics.

Please enquire for more information about 3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoxazole including the price, delivery time and more detailed product information at the technical inquiry form on this page

S09600 - Hexamethyldisilane

Benzyltriethoxysilane is a polymer film cross-linking agent that is used in cationic polymerization reactions. It reacts with hydroxyl groups on the surface of metal and forms an Si-O-Si bond. This product has been shown to be reactive with human serum and can be used as a coating for medical devices. The use of benzyltriethoxysilane as a coating on contact lenses has been shown to reduce the risk of eye infections by microorganisms such as Staphylococcus aureus, which can cause corneal ulcers. Benzyltriethoxysilane can also be used as an optical sensor for hydrogen fluoride gas. It changes from yellow to colorless when it reacts with hydrogen fluoride gas.

Applications Trimethylboroxin (50% Solution in THF) is used in a diverse array of areas, including as a polymerization additive. Trimethylboroxin is also used in the preparation of CBS catalysts for asymmetric reductions. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Gilmore, N., et al.: Tetrahedron Asy., 14, 2115 (2003); Najera, C., et al.: Adv. Synth. Catal., 346, 1798 (2004);

S20280 - 5-Trimethylsilylthiazole

(R)-(+)-2-Methyl-CBS-oxazaborolidine is a dpp-iv inhibitor that is a β-unsaturated ketone. It has been shown to inhibit the enzyme histone lysine demethylase, which may be involved in the regulation of bone mass. This compound also has a pharmacokinetic profile that is characterized by high oral bioavailability, low plasma protein binding, and rapid metabolism by liver enzymes. The reaction mechanism for this compound is based on the formation of an enolate carbanion. (R)-(+)-2-Methyl-CBS-oxazaborolidine can be synthesized with high stereoselectivity and yields from reactions with simple starting materials. This synthetic route also has a number of advantages over other methods: it does not require any protecting groups, it does not use toxic solvents such as dichloromethane or chloroform, and it can be performed in anhydrous conditions

Please enquire for more information about 5-Fluoro-2-methylpyridin-4-yl Boronic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about [4-Methoxy-2-(1H-pyrazol-1-yl)phenyl]boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Carboxy-3-chlorophenylboronic acid is a pharmacological agent that has antiviral properties. It is a singlet oxygen emitting compound and can be used in the development of new strategies for antiviral therapy. 4-Carboxy-3-chlorophenylboronic acid has been shown to inhibit virus growth by blocking viral replication and inhibiting the release of single strand RNA from cells infected with influenza A virus. This compound also inhibits the activity of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase, which plays an important role in HIV infection. The emission spectrum of this compound was analysed using nanometric techniques and it has been shown to emit singlet oxygen under UV irradiation.

S05230 - Cyclohexyltrimethoxysilane

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S13600 - Phenylsilane

Tris(trimethylsilyl)silane is a reactive functional group that is used in the synthesis of monoclonal antibodies. It reacts with halides to form an intermediate, which then undergoes chain reactions with other molecules to form the final product. Tris(trimethylsilyl)silane can be used for cancer therapy and for the detection of antibodies. It has been shown that tris(trimethylsilyl)silane will react with a light emitting compound (e.g., 4-dimethylaminopyridine) and a cationic polymerization initiator (e.g., diallyldimethylammonium chloride). This reaction produces high values of light emission, which can be detected by x-ray crystal structures.

Please enquire for more information about Benzo-2,1,3-thiadiazole-4-boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

S03129 - 3-Bromo-1-triisopropylsilyl pyrrole