CAS 847818-62-6
:Boronic acid, B-(1,3,5-trimethyl-1H-pyrazol-4-yl)-
Description:
Boronic acid, B-(1,3,5-trimethyl-1H-pyrazol-4-yl)-, with the CAS number 847818-62-6, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyrazole ring. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the trimethyl-substituted pyrazole moiety contributes to its unique reactivity and solubility characteristics. Boronic acids are known for their role in Suzuki coupling reactions, which are vital for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, this compound may exhibit biological activity, potentially serving as a pharmacophore in drug development. Its stability, solubility in polar solvents, and ability to participate in Lewis acid-base interactions further enhance its utility in chemical research and applications.
Formula:C6H11BN2O2
Synonyms:- Boronicacid, (1,3,5-trimethyl-1H-pyrazol-4-yl)-
- (1,3,5-Trimethyl-1H-pyrazol-4-yl)boronic acid
- (1,3,5-Trimethylpyrazol-4-yl)boronicacid
- 1,3,5-TriMethylpyrazole-4-boronic acid
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Found 4 products.
(1,3,5-Trimethyl-1H-pyrazol-4-yl)boronic acid
CAS:Formula:C6H11BN2O2Purity:97%Color and Shape:SolidMolecular weight:153.97471,3,5-Trimethylpyrazole-4-boronic acid
CAS:1,3,5-Trimethylpyrazole-4-boronic acidPurity:96%Molecular weight:153.97g/mol(1,3,5-Trimethyl-1H-pyrazol-4-yl)boronic acid
CAS:Formula:C6H11BN2O2Purity:97%Color and Shape:Liquid, No data available.Molecular weight:153.98(1,3,5-Trimethylpyrazol-4-yl)boronic Acid-d3
CAS:Controlled ProductFormula:C6D3H8BN2O2Color and Shape:NeatMolecular weight:156.993



