Organoboranes

Stability Moisture Sensitive
Applications Chlorotriethylsilane is used in the preparation of potent silylating agent and lewis acid catalyst. Chlorotriethylsilane derivatived ethers have been shown to be more stable towards hydrolysis than are trimethyl ethers.
E0
References Alvisi, C. et al.: J. Org. Chem., 63, 1330 (1998): Higashiya, S. et al.: J. Org. Chem., 69, 6326 (2004); Hicks, J.D. et al.: Org. Lett., 9, 5621 (2007);

Applications 3-Formylphenylboronic Acid is a reactant in the synthesis of I-BET726 (GSK1324726A), a potent tetrahydroquinoline ApoA1 up-regulator and selective BET bromodomain inhibitor.
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 Gosmini, R., et. al.: J. Med. Chem., 57, 8111 (2014)

Applications Allylboronic acid pinacol ester
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications 5-Ethyl-2-fluorophenylboronic acid

Applications 5-Bromopentylboronic Acid

Applications methyl 4-(bromomethyl)-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (cas# 1626407-50-8) is a useful research chemical.

Applications 4-[[[(1,1-Dimethylethyl)diphenylsilyl]oxy]methyl]-2,2-dimethyl-1,3-dioxolane is an intermediate in the synthesis of 1,2-Dioleoyl-rac-glycerol (D482175), which is an analog of 1,3-Dioleoylglycerol (D484210) which is used in the synthesis of amphiphilic gadolinium complexes as MRI contrast agents.
References Accardo, A., et. al.: J. Mater. Chem. B., 1, 617 (2013)

Applications tert-Butyldimethyl(4-(nitrosophenyl)butoxy)silane is an intermediate used in the synthesis of (E)-S-(3-((4-((4-(4-hydroxybutyl)phenyl)diazenyl)phenyl)amino)-3-oxopropyl) methanesulfonothioate (H895230), which is a useful research chemical.

Applications (E)-2-(1-Butenyl)-1,3,2-benzodioxaborole (cas# 106094-36-4) is a compound useful in organic synthesis.

Applications tert-Butyl-(3-iodo-1,1-dimethyl-propoxy)-dimethyl-silane (cas# 105262-85-9) is used as a reagent in the preparation of Methyl Acetoacetate.
References Heslin, J. C., et al.: J. Chem. Soc. [Perkin 1]. 6, 1417 (1988)

Stability Acid Sensitive
Applications 2-tert-Butyldimethylsilyloxyethanol (cas# 102229-10-7) is a compound useful in organic synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications Benzo[b]thien-3-ylboronic acid is used in the synthesis and evaluation of dual wavelength fluorescent benzo[b]thiophene boronic acid derivatives for sugar/glycoprotein sensing.
References Akay, S., et al.: Chem. Biol. Drug Des., 70, 279 (2007)

Applications N-Pentylboronic Acid is used in the synthesis of (-)-Δ8-THC and (-)-Δ9-THC. Also it aids in the synthesis of boronic acid inhibitors of endothelial lipase.
References O'Connell, D. et al.: Bioorg. Med. Chem. Lett., 22, 1397 (2012); Cheng, L. et al.: Org. Lett., 15, 764 (2013);

Applications 1,1,1,5,7,7,7-Heptamethyl-3,3-bis[(trimethylsilyl)oxy]tetrasiloxane is used in the analysis of organosilicon compounds (eg hexamethyldisiloxane) using gas chromatography or mass spectrometry.
References Wurst, M., et al.: Chromatographia, 6, 359 (1973), Wurst, M.: Chemicky Prumysl, 22, 124 (1972)

Applications 2-Carboxyfuran-5-boronic acid, pinacol ester

Applications Di(p-anisyl)iodonium Tetrafluoborate (cas# 1426-58-0) is a compound useful in organic synthesis.

Applications Dimethoxy(methyl)silane (cas# 16881-77-9) is a useful research chemical.

Applications 1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-ol is used as a reagent in the synthesis of P4-benzoxaborole-substituted macrocyclic inhibitors of HCV NS3 protease.
References Ding, C.Z., et al.: Bioorg. Med. Chem. Lett., 20, 7317 (2010)

Applications Benzothiophene-5-boronic acid

Applications Nitro(trimethylsilyl)acetylene acts as a reagent in the synthesis, reactions, complexes, and properties of nitroalkynes as a unique class of energetic materials. Synthesis of nitro(trimethylsilyl)acetylene.
References Windler, G. K., et al.: Synthesis, 46, 2383 (2014); Schmitt, R. J., et al.: Synthesis, 2, 123 (1986)

Applications (4-((4aR)-7-(Benzyloxy)-3,4,4a,5-tetrahydro-2H-chromen-3-yl)phenoxy)(tert-butyl)dimethylsilane is an protected intermediate in the synthesis of isoflavone Daidzein (D103500) related compounds.

Applications TETRAMETHYLAMMONIUM BOROHYDRIDE (cas# 16883-45-7) is a useful research chemical.

Applications 5-Formylfuran-2-boronic Acid Neopentyl Glycol Ester is a useful reagent in lapatinib synthesis.
References Radl, S., et al.: PCT Int. Appl. (2014), WO 2014059956 A1

Please enquire for more information about 2-[4-(tert-Butyldimethylsilyloxymethyl)-2-nitrophenoxy]acetic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

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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.

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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.

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.

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.

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. !-- -->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

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.

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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.

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