CAS 953411-07-9: B-(6-Methyl-1H-indol-2-yl)boronic acid

Description: B-(6-Methyl-1H-indol-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a 6-methyl-1H-indole moiety. This compound typically exhibits properties associated with both boronic acids and indole derivatives, including potential applications in medicinal chemistry and organic synthesis. The boronic acid group allows for reversible covalent bonding with diols, making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. The indole structure contributes to its biological activity, as indoles are known for their presence in many natural products and pharmaceuticals. Additionally, the methyl group at the 6-position can influence the compound's solubility, reactivity, and interaction with biological targets. Overall, B-(6-Methyl-1H-indol-2-yl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

Formula: C₉H₁₀BNO₂

InChI: InChI=1S/C9H10BNO2/c1-6-2-3-7-5-9(10(12)13)11-8(7)4-6/h2-5,11-13H,1H3

InChI key: InChIKey=LFXUSTLDJZUIJL-UHFFFAOYSA-N

SMILES: OB(O)C1=CC=2C=CC(=CC2N1)C

Synonyms:

• Boronic acid, B-(6-methyl-1H-indol-2-yl)-
• B-(6-Methyl-1H-indol-2-yl)boronic acid
• (6-Methyl-1H-indol-2-yl)boronic acid

(6-Methyl-1H-indol-2-yl)boronic acid

CAS: 953411-07-9

• Formula: C₉H₁₀BNO₂
• Molecular weight: 174.9922

3-(3-Chlorophenyl)-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine dihydrochloride

CAS: 953411-07-9

Versatile small molecule scaffold

• Formula: C₉H₁₀BNO₂
• Purity: Min. 95%
• Molecular weight: 174.99 g/mol