CAS 2121513-84-4: B-(7-Fluoro-1H-indazol-4-yl)boronic acid

Description: B-(7-Fluoro-1H-indazol-4-yl)boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group, specifically an indazole moiety substituted with a fluorine atom. 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 fluorine substitution can enhance the compound's biological activity and lipophilicity, potentially influencing its pharmacokinetic properties. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's structure suggests it may also interact with biological targets, making it a candidate for further investigation in drug development. Overall, B-(7-Fluoro-1H-indazol-4-yl)boronic acid represents a versatile building block in both synthetic and medicinal chemistry contexts.

Formula: C₇H₆BFN₂O₂

InChI: InChI=1S/C7H6BFN2O2/c9-6-2-1-5(8(12)13)4-3-10-11-7(4)6/h1-3,12-13H,(H,10,11)

InChI key: InChIKey=QOWKDTSMJKVPRP-UHFFFAOYSA-N

SMILES: FC1=CC=C(B(O)O)C=2C=NNC12

Synonyms:

• B-(7-Fluoro-1H-indazol-4-yl)boronic acid
• Boronic acid, B-(7-fluoro-1H-indazol-4-yl)-

7-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

CAS: 2121513-84-4

• Formula: C₇H₆BFN₂O₂
• Purity: 95%
• Molecular weight: 179.9441

(7-fluoro-2H-indazol-4-yl)boronic acid

CAS: 2121513-84-4

• Purity: 98%
• Molecular weight: 179.9499969482422

(7-Fluoro-1H-indazol-4-yl)boronic acid

CAS: 2121513-84-4

Versatile small molecule scaffold

• Formula: C₇H₆BFN₂O₂
• Purity: Min. 95%
• Molecular weight: 179.95 g/mol