CAS 1451390-95-6: B-[2,4-Difluoro-3-(1-methylethoxy)phenyl]boronic acid

Description: B-[2,4-Difluoro-3-(1-methylethoxy)phenyl]boronic 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, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with two fluorine atoms at the 2 and 4 positions, enhancing its electronic properties and potentially influencing its reactivity. The presence of the 1-methylethoxy group contributes to its solubility and steric properties, which can affect its interaction with biological targets or other chemical species. This compound is typically used in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds, and may also exhibit interesting biological activities due to its structural characteristics. As with many boronic acids, it is important to handle this substance with care, considering its potential reactivity and the need for appropriate storage conditions to maintain stability.

Formula: C₉H₁₁BF₂O₃

InChI: InChI=1S/C9H11BF2O3/c1-5(2)15-9-7(11)4-3-6(8(9)12)10(13)14/h3-5,13-14H,1-2H3

InChI key: InChIKey=LTXLJWCQTYVYCS-UHFFFAOYSA-N

SMILES: FC1=CC=C(B(O)O)C(F)=C1OC(C)C

Synonyms:

• Boronic acid, B-[2,4-difluoro-3-(1-methylethoxy)phenyl]-
• B-[2,4-Difluoro-3-(1-methylethoxy)phenyl]boronic acid

2,4-Difluoro-3-isopropoxyphenylboronic acid

CAS: 1451390-95-6

• Formula: C₉H₁₁BF₂O₃
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 215.9896

(2,4-Difluoro-3-isopropoxyphenyl)boronic acid

CAS: 1451390-95-6

• Purity: 98%
• Molecular weight: 215.99000549316406

2,4-Difluoro-3-isopropoxyphenylboronic acid

CAS: 1451390-95-6

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• Formula: C₉H₁₁BF₂O₃
• Purity: Min. 95%
• Molecular weight: 215.99 g/mol