CAS 1310404-47-7: B-(3-Methyl-1H-indazol-7-yl)boronic acid

Description: B-(3-Methyl-1H-indazol-7-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a 3-methyl-1H-indazole 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 indazole ring contributes to its aromaticity and potential biological activity, which may include interactions with specific enzymes or receptors. The presence of the methyl group can influence the compound's solubility and reactivity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are essential in the formation of carbon-carbon bonds in organic synthesis. Overall, B-(3-Methyl-1H-indazol-7-yl)boronic acid is a versatile compound with potential applications in drug development and materials science, owing to its unique structural features and reactivity.

Formula: C₈H₉BN₂O₂

InChI: InChI=1S/C8H9BN2O2/c1-5-6-3-2-4-7(9(12)13)8(6)11-10-5/h2-4,12-13H,1H3,(H,10,11)

InChI key: InChIKey=NOECVYNEVSUQPU-UHFFFAOYSA-N

SMILES: OB(O)C1=CC=CC=2C(=NNC12)C

Synonyms:

• B-(3-Methyl-1H-indazol-7-yl)boronic acid
• Boronic acid, B-(3-methyl-1H-indazol-7-yl)-

Boronic acid, B-(3-methyl-1H-indazol-7-yl)-

CAS: 1310404-47-7

• Formula: C₈H₉BN₂O₂
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 175.98026000000002

3-Methyl-1H-indazole-7-boronic acid

CAS: 1310404-47-7

• Molecular weight: 175.98g/mol

3-METHYL-1H-INDAZOLE-7-BORONIC ACID

CAS: 1310404-47-7

• Purity: 95.0%
• Molecular weight: 175.97999572753906

(3-methyl-1H-indazol-7-yl)boronic acid

CAS: 1310404-47-7

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• Formula: C₈H₉BN₂O₂
• Purity: Min. 95%
• Molecular weight: 175.98 g/mol