CAS 1072951-50-8: 2-Hydroxy-4-trifluoromethylphenylboronic acid

Description: 2-Hydroxy-4-trifluoromethylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. This compound features a hydroxyl group and a trifluoromethyl group attached to a phenyl ring, contributing to its unique chemical properties. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the compound may exhibit interesting interactions with biological targets due to its structural features, making it a candidate for further research in drug development. Its solubility and stability in various solvents can vary, which is important for its practical applications in laboratory settings. Overall, 2-Hydroxy-4-trifluoromethylphenylboronic acid is a versatile compound with significant implications in synthetic and medicinal chemistry.

(2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid

CAS: 1072951-50-8

• Formula: C₇H₆BF₃O₃
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 205.9269

2-Hydroxy-4-trifluoromethylphenylboronic acid

CAS: 1072951-50-8

• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 205.93g/mol

(2-Hydroxy-4-(trifluoromethyl)phenyl)boronic acid

CAS: 1072951-50-8

• Purity: 95.0%
• Molecular weight: 205.92999267578125

2-Hydroxy-4-trifluoromethylphenylboronic acid

CAS: 1072951-50-8

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• Formula: C₇H₆BF₃O₃
• Purity: Min. 95%
• Molecular weight: 205.93 g/mol