CAS 1451392-93-0: B-[2-Formyl-6-(trifluoromethyl)phenyl]boronic acid

Description: B-[2-Formyl-6-(trifluoromethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic synthesis applications, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a formyl group and a trifluoromethyl group, which can significantly influence its electronic properties and reactivity. The trifluoromethyl group is known for its electron-withdrawing characteristics, enhancing the acidity of the boronic acid moiety. This compound is typically used in medicinal chemistry and materials science due to its ability to form stable complexes with diols and its utility in the synthesis of complex organic molecules. Additionally, the presence of the formyl group allows for further functionalization, making it a versatile intermediate in organic synthesis. Its unique structural features contribute to its potential applications in drug development and the creation of novel materials.

Formula: C₈H₆BF₃O₃

InChI: InChI=1S/C8H6BF3O3/c10-8(11,12)6-3-1-2-5(4-13)7(6)9(14)15/h1-4,14-15H

InChI key: InChIKey=VYQNGLZQQFGULH-UHFFFAOYSA-N

SMILES: O=CC1=CC=CC(=C1B(O)O)C(F)(F)F

[2-Formyl-6-(trifluoromethyl)phenyl]boronicacid

CAS: 1451392-93-0

• Formula: C₈H₆BF₃O₃
• Purity: 95%
• Molecular weight: 217.9376

(2-Formyl-6-(trifluoromethyl)phenyl)boronic acid

CAS: 1451392-93-0

• Purity: 98+%
• Molecular weight: 217.94000244140625

[2-Formyl-6-(trifluoromethyl)phenyl]boronic acid

CAS: 1451392-93-0

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• Formula: C₈H₆BF₃O₃
• Purity: Min. 95%
• Molecular weight: 217.94 g/mol