
Organoborane
6123 produits trouvés pour "Organoborane"
Tetrahydropyran-4-boronicacid
CAS :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 pageFormule :C5H11BO3Degré de pureté :Min. 95%Masse moléculaire :129.95 g/mol4-[4-(N-Boc)piperazin-1-yl]phenylboronic acid pinacol ester
CAS :Please enquire for more information about 4-[4-(N-Boc)piperazin-1-yl]phenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C21H33BN2O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :388.31 g/molFmoc-epsilon-aminocaproic acid-Wang resin (200-400 mesh)
Please enquire for more information about Fmoc-epsilon-aminocaproic acid-Wang resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this pageDegré de pureté :Min. 95%Bobbitt's salt
CAS :4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium tetrafluoroborate, most commonly known as Bobbitt's salt, is a cheap and benign oxidant. It’s an oxoamonium salt that is used in oxidative cleveage of C-C and C-O bonds. The most common application of Bobbitt's salts is as a catalyst for the synthesis of dimethylbenzoquinones or DMBQs.
Formule :C11H21BF4N2O2Degré de pureté :Min. 95%Couleur et forme :Red PowderMasse moléculaire :300.1 g/molN-alpha-Trityl-Nepsilon-Fmoc-L-lysine
CAS :N-alpha-Trityl-Nepsilon-Fmoc-L-lysine is a pentapeptide that is used in peptides. It has been shown to have cytotoxicity and permeability, as well as being biologically active. N-alpha-Trityl-Nepsilon-Fmoc-L-lysine has also been used in solid phase synthesis of peptides. This pentapeptide can be synthesized using the Miyaura cross coupling reaction with an ether or Suzuki cross coupling reaction. N-alpha-Trityl-Nepsilon-Fmoc-L-lysine is a bicyclic molecule that can be synthesized on a solid phase.Formule :C40H38N2O4Degré de pureté :Min. 95%Masse moléculaire :610.74 g/mol(1-Methyl-1H-pyrazol-4-yl)boronic acid
CAS :(1-Methyl-1H-pyrazol-4-yl)boronic acid is a boronic acid that has been used for the synthesis of a number of heterocyclic compounds. Boronic acids are commonly used to synthesize phosphine ligands, which are reactive and can be used in cross-coupling reactions with organic halides, triflates, and tosylates. The efficiency of the reaction depends on the functional group present on the boron atom. (1-Methyl-1H-pyrazol-4-yl)boronic acid can inhibit the activity of many types of enzymes, including those involved in bacterial DNA synthesis and protein synthesis. (1-Methyl-1H-pyrazol-4-yl)boronic acid has been shown to have pharmacokinetic properties that depend on its ionization state.Formule :C4H7BN2O2Degré de pureté :Min. 95%Masse moléculaire :125.92 g/mol(Chlorodifluoromethyl)trimethylsilane
CAS :(Chlorodifluoromethyl)trimethylsilane is a chlorinating agent that is used for the transfer of chlorine to organic compounds. The activated chlorides are converted to aldehydes, which are then reacted with terminal alkynes in the presence of sodium carbonate to produce (chlorodifluoromethyl)trimethylsilanes. This reaction produces an organosilicon compound that has been shown to inhibit certain enzymes, such as lipases and proteases. Chlorodifluoromethyl)trimethylsilane also has bioisosteres, or structural analogs, with other halogens. It can be prepared by irradiation of chlorodichloromethane at room temperature in the presence of a catalyst.Formule :C4H9ClF2SiDegré de pureté :Min. 95%Couleur et forme :Colorless PowderMasse moléculaire :158.65 g/mol4-Acetamidophenyl boronic acid
CAS :4-Acetamidophenyl boronic acid is a cross-coupling reagent that has been used in the synthesis of a variety of organic molecules. The reaction is stereoselective and proceeds with high yield. 4-Acetamidophenyl boronic acid has also been used to synthesize amides and azobenzenes, which can be substituted with chloride or uv irradiation to give chloroazobenzene or benzotriazole respectively. 4-Acetamidophenyl boronic acid has shown potent inhibition against the enzyme cyclooxygenase 2 (COX2) and acidic hydrolysis.
Degré de pureté :Min. 95%4-Methoxycarbonylphenylboronic acid
CAS :4-Methoxycarbonylphenylboronic acid is an organic compound that can be synthesized from biphenyl. It is a diazonium salt with a bidentate ligand and a carbonyl group, which allows it to form an intermolecular hydrogen bond. The phenyl group of 4-methoxycarbonylphenylboronic acid can be oxidized to the corresponding carboxylic acid or reduced to the corresponding alcohol. 4-Methoxycarbonylphenylboronic acid is also soluble in halides, iodinations, and mercaptoacetic acid. This compound has been used as an acceptor in the oxidation of aluminium with diborane as a catalyst. 4-Methoxycarbonylphenylboronic acid has also been used to synthesize other compounds such as metronidazole (a drug) and erythromycin (an antibiotic).Formule :C8H9BO4Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :179.97 g/mol3-Pyridineboronic acid
CAS :3-Pyridineboronic acid is an antimicrobial agent that is used to treat bacterial and fungal infections. 3-Pyridineboronic acid is a prodrug that is metabolized to its active form, pyridinium boronate. This drug has been shown to be effective in the treatment of hypoxic tumors in mice, which are resistant to other anticancer drugs. 3-Pyridineboronic acid also has acidic properties and can be used as an antiseptic for the treatment of skin and eye infections. It can also be used as a hydrogen bonding partner when combined with halides, such as chloride or bromide ions. The drug binds to human serum proteins and forms an acidic complex that prevents bacterial growth by inhibiting protein synthesis. 3-Pyridineboronic acid also inhibits prostate cancer cells by competitively inhibiting the enzyme 4-pyridinylboronic acid reductase (4PBAR).Formule :C5H6BNO2Degré de pureté :Min. 95%Masse moléculaire :122.92 g/molBis (neopentylglycolato) diboron
CAS :Bis (neopentylglycolato) diboron is a boronic acid that can be used in catalytic asymmetric synthesis. The compound is prepared by the reaction of neopentyl glycol with boric acid and NaOH, followed by purification by column chromatography. Bis (neopentylglycolato) diboron is soluble in non-polar solvents. It has been shown to have uptake in cells and has been used in the preparation of conjugates for the treatment of cancer.Formule :C10H20O4B2Degré de pureté :Min. 95%Couleur et forme :White Off-White PowderMasse moléculaire :225.89 g/mol4-Methoxyphenyl boronic acid
CAS :4-Methoxyphenyl boronic acid is a molecule with a hydroxyl group and a boronic acid. It is synthesized by reacting biphenyl with trifluoroacetic acid in the presence of sodium carbonate and palladium-catalyzed coupling. 4-Methoxyphenyl boronic acid has shown to bind to the receptor for fatty acids, which may be due to its structural similarity to p-hydroxybenzoic acid. The protonated form of this molecule has been shown to react with an electrophilic carbon atom and an electron-deficient alkyl or vinyl halide, resulting in ring formation. This reaction is known as the Suzuki coupling reaction.Formule :C7H9BO3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :151.96 g/mol4-Mercaptophenylboronic acid
CAS :4-Mercaptophenylboronicacid is a boronic acid that has been used to synthesize gold nanoparticles with antimicrobial properties. Boronic acids are able to form hydrogen bonds with biological molecules such as proteins and DNA, which allows them to be used for immobilization of biomolecules. This compound is also used as a reagent for the synthesis of disulfide bonds in proteins and peptides. 4-Mercaptophenylboronicacid can be used to prepare samples for electrochemical impedance spectroscopy (EIS) and colorimetric analysis.Formule :C6H7BO2SDegré de pureté :Min. 95%Masse moléculaire :154 g/mol4-Hydroxyphenylboronic acid
CAS :4-Hydroxyphenylboronic acid is a potential anticancer agent that has been studied in vitro and in vivo. It has been shown to inhibit the activity of p-glycoprotein, which is a protein that pumps drugs out of cells, and it is also an inhibitor of lipid kinase. 4-Hydroxyphenylboronic acid binds to the ATP binding site of the enzyme and forms covalent bonds with Lys residues on the enzyme, inhibiting its function. The compound can be detected at low concentrations using fluorescence or chemiluminescence techniques. This compound may have therapeutic benefits for antimicrobial agents as well as for cancer treatment.Formule :C6H7BO3Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :137.93 g/mol2-(4,4-Difluorocyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS :Please enquire for more information about 2-(4,4-Difluorocyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C12H19BF2O2Degré de pureté :Min. 95%Masse moléculaire :244.09 g/mol2-Pyridineboronic acid
CAS :2-Pyridineboronic acid is a chemical compound that belongs to the group of quinoline derivatives. It is used in pharmaceutical preparations, including as an intermediate for the synthesis of other compounds. 2-Pyridineboronic acid has been shown to have antiproliferative effects on cancer cells and has been found to be active against nicotinic acetylcholine receptors (NAR). The compound also inhibits lipid kinase activity, which is involved in the production of phosphatidylcholine and phosphatidylethanolamine from phosphatidylserine. 2-Pyridineboronic acid can react with hydrochloric acid and electrochemical impedance spectroscopy to produce a solution that has a detection time of about 10 minutes.Formule :C5H6BNO2Degré de pureté :Min. 95%Masse moléculaire :122.92 g/mol3-Pyridylboronic acid pinacol ester
CAS :3-Pyridylboronic acid pinacol ester is a versatile reagent that can be used in the synthesis of polymers with reactive functionalities. This compound is a crosslinker, which means that it reacts with two or more other molecules to form a covalent bond. 3-Pyridylboronic acid pinacol ester has been shown to react with ring-opening methacrylate monomers and expand their polymer backbone, which leads to an increase in the number of reactive groups on the chain. The introduction of 3-pyridylboronic acid pinacol ester can also introduce fluorescent units into polymers for use as probes for biological systems. There are many possible applications for this versatile reagent, including its use in the synthesis of imidazopyridine ligands.
Formule :C11H16BNO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :205.06 g/molN-alpha-Fmoc-Nepsilon-allyloxycarbonyl-D-lysine
CAS :N-alpha-Fmoc-Nepsilon-allyloxycarbonyl-D-lysine is a medicament that is modified with an amino group at the alpha position. It is synthesized by modification of the chain with a ganirelix acetate. N-alpha-Fmoc-Nepsilon-allyloxycarbonyl-D-lysine can be used to produce ganirelix, which inhibits the release of follicle stimulating hormone (FSH). The chemical synthesis of this drug has been shown to be successful in large scale production, and it has been shown to be effective in treating patients with prostate cancer. Impurities in this drug have been found and treated by removing the methyl ester group from the lysine residue.Formule :C25H28N2O6Degré de pureté :Min. 95%Masse moléculaire :452.5 g/molBiotinyl-ε-aminocaproyl-D-Phe-Pro-Arg-chloromethylketone
CAS :Please enquire for more information about Biotinyl-ε-aminocaproyl-D-Phe-Pro-Arg-chloromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C37H56ClN9O6SDegré de pureté :Min. 95%Masse moléculaire :790.42 g/mol4-Chlorophenylboronic acid
CAS :4-Chlorophenylboronic acid is a chemical compound that is used in the industrial preparation of biphenyl. It is produced by the Friedel-Crafts reaction between chlorine and 4-methoxyphenylboronic acid. This reaction can be carried out using a variety of solvents, such as chloroform or carbon tetrachloride. The optimal reaction conditions are acidic pH values, which are achieved by adding sodium carbonate to the solution. The product can be purified by distillation or crystallization. 4-Chlorophenylboronic acid can also be used for the synthesis of organic compounds through cross-coupling reactions with organometallic reagents, such as palladium chloride and triphenylphosphine, or through asymmetric synthesis with chiral ligands like (S)-proline and 2-(diphenylphosphino)ferrocene.Formule :C6H6BClO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :156.37 g/mol
