CAS 1451390-89-8: B-[2-Formyl-5-(1-methylethyl)phenyl]boronic acid

Description: B-[2-Formyl-5-(1-methylethyl)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 an isopropyl group, contributing to its unique chemical properties. The presence of the formyl group indicates that it can participate in further reactions, such as condensation or reduction, while the boronic acid moiety allows for the formation of stable complexes with diols and other Lewis bases. This compound is typically used in medicinal chemistry and materials science due to its ability to form covalent bonds with biological molecules and its potential role in drug development. Additionally, its structural characteristics may influence its solubility, stability, and reactivity, making it a valuable compound for research in synthetic organic chemistry.

Formula: C₁₀H₁₃BO₃

InChI: InChI=1S/C10H13BO3/c1-7(2)8-3-4-9(6-12)10(5-8)11(13)14/h3-7,13-14H,1-2H3

InChI key: InChIKey=OUMRDYQDMKOJKZ-UHFFFAOYSA-N

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

Synonyms:

• B-[2-Formyl-5-(1-methylethyl)phenyl]boronic acid
• Boronic acid, B-[2-formyl-5-(1-methylethyl)phenyl]-

2-Formyl-5-isopropylphenylboronic acid

CAS: 1451390-89-8

• Formula: C₁₀H₁₃BO₃
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 192.0194

2-Formyl-5-isopropylphenylboronic acid

CAS: 1451390-89-8

• Purity: 98%
• Molecular weight: 192.02000427246094

(2-Formyl-5-isopropylphenyl)boronic acid

CAS: 1451390-89-8

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• Formula: C₁₀H₁₃BO₃
• Purity: Min. 95%
• Molecular weight: 192.02 g/mol