Organoboranes
Found 6123 products of "Organoboranes"
2-Chloro-3-ethylbenzoxazolium tetrafluoroborate
CAS: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.Formula:C9H9BClF4NOPurity:Min. 95%Color and Shape:PowderMolecular weight:269.43 g/molm-Carborane
CAS:Controlled Productm-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.Formula:C2H12B10Purity:Min. 95%Color and Shape:White powder(solid)Molecular weight:144.23 g/molTriethyl borate
CAS: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.
Formula:C6H15BO3Purity:Min. 95%Molecular weight:145.99 g/mol2,5-Bis(4-bromophenyl)-1,1-dimethyl-3,4-diphenylsilole
CAS: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 pageFormula:C30H24Br2SiPurity:Min. 95%Molecular weight:572.41 g/molN-Hexylboronic acid
CAS: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.Formula:C6H15BO2Purity:Min. 95%Molecular weight:129.99 g/mol1-Methylindole-3-boronic acid pinacol ester
CAS:Please enquire for more information about 1-Methylindole-3-boronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C15H20BNO2Purity:Min. 95%Molecular weight:257.14 g/molE-Hexen-1-ylboronic acid
CAS:E-Hexen-1-ylboronic acid is a reactive, boron-containing compound that can be used for Suzuki coupling reactions and metathesis reactions. It is also useful in the analysis of organic compounds, due to its ability to form brightly coloured complexes with metal ions. E-Hexen-1-ylboronic acid has been shown to react with chloride, reoxidant and hexane. This compound can be used as an analytical reagent for the detection of stereoselectively in a stepwise reaction. E-Hexen-1-ylboronic acid forms crystals x-ray diffraction patterns that are characteristic of a chair conformation.Formula:C6H13BO2Purity:Min. 95%Molecular weight:127.98 g/mol4-(N-Methylamino)phenylboronic acid pinacol ester
CAS: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
Formula:C13H20BNO2Purity:Min. 95%Molecular weight:233.11 g/mol3-Chloro-4-cyanophenylboronic acid
CAS:Controlled ProductPlease enquire for more information about 3-Chloro-4-cyanophenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C7H5BClNO2Purity:Min. 95%Molecular weight:181.38 g/mol4-(4-Oxopiperidine-1-carbonyl)phenylboronic acid
CAS:Controlled ProductPlease 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 pageFormula:C12H14BNO4Purity:Min. 95%Molecular weight:247.05 g/mol(3-Mercaptopropyl)trimethoxysilane
CAS: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 synergisticFormula:C6H16O3SSiPurity:Min. 98 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:196.34 g/mol2-(Dimethylaminocarbonyl)ethylboronic acid, pinacol ester
CAS:Please enquire for more information about 2-(Dimethylaminocarbonyl)ethylboronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C11H22BNO3Purity:Min. 95%Molecular weight:227.11 g/molTrimethylchlorosilane
CAS: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.
Formula:C3H9ClSiPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:108.64 g/mol(trans)-2-Cyclopropylvinylboronic acid pinacol ester
CAS:Please enquire for more information about (trans)-2-Cyclopropylvinylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C11H19BO2Purity:Min. 95%Molecular weight:194.08 g/molTetramethylammonium triacetoxyborohydride
CAS: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.
Formula:C10H22BNO6Purity:Min. 95%Color and Shape:White PowderMolecular weight:263.1 g/mol5-Fluoropyridine-2-boronic acid
CAS:Please enquire for more information about 5-Fluoropyridine-2-boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C5H5BFNO2Purity:Min. 95%Molecular weight:140.91 g/mol4-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)
CAS: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.
Formula:C7H6BF3O3Purity:Min. 95%Molecular weight:205.93 g/molTriethoxy(propyl)silane
CAS: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.Formula:C9H22O3SiPurity:Min. 95%Molecular weight:206.35 g/molNonafluorohexyltrichlorosilane
CAS: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.
Formula:C6H4Cl3F9SiPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:381.53 g/mol9,9-Bis(2-ethylhexyl)fluorene-2,7-bis(boronic acidpinacolester)
CAS: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
Formula:C41H64B2O4Purity:Min. 95%Molecular weight:642.57 g/mol
