CAS 1361233-94-4: B-(3-Methyl-1H-indol-6-yl)boronic acid

Description: B-(3-Methyl-1H-indol-6-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a 3-methyl-1H-indole moiety. 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 indole structure contributes to its potential biological activity, as indoles are known for their presence in many natural products and pharmaceuticals. The compound is likely to be a solid at room temperature and may have moderate solubility in polar solvents due to the presence of the boronic acid group. Its reactivity can be influenced by the pH of the environment, as boronic acids can exist in different forms depending on protonation. Overall, B-(3-Methyl-1H-indol-6-yl)boronic acid is a versatile compound with potential applications in drug development and materials science.

Formula: C₉H₁₀BNO₂

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

InChI key: InChIKey=VCGNVVDDGOIIMG-UHFFFAOYSA-N

SMILES: OB(O)C=1C=CC2=C(C1)NC=C2C

Synonyms:

• Boronic acid, B-(3-methyl-1H-indol-6-yl)-
• B-(3-Methyl-1H-indol-6-yl)boronic acid

3-methyl-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

CAS: 1361233-94-4

• Formula: C₉H₁₀BNO₂
• Molecular weight: 174.9922

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

CAS: 1361233-94-4

• Purity: 98%
• Molecular weight: 174.99000549316406

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

CAS: 1361233-94-4

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