CAS 211495-36-2

B-[2-(1-Methylethyl)-4-(phenylmethoxy)phenyl]boronic acid

Description:

B-[2-(1-Methylethyl)-4-(phenylmethoxy)phenyl]boronic acid, identified by its CAS number 211495-36-2, is an organoboron compound characterized by the presence of a boronic acid functional group. This compound features a phenyl ring substituted with a phenylmethoxy group and an isopropyl group, contributing to its unique structural properties. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis, medicinal chemistry, and materials science. The presence of the isopropyl and phenylmethoxy substituents enhances its lipophilicity and may influence its reactivity and solubility in organic solvents. Additionally, boronic acids can participate in Suzuki coupling reactions, which are essential for constructing complex organic molecules. Overall, this compound's structural characteristics suggest potential utility in drug development and as a building block in organic synthesis.

Formula: C₁₆H₁₉BO₃

InChI: InChI=1S/C16H19BO3/c1-12(2)15-10-14(8-9-16(15)17(18)19)20-11-13-6-4-3-5-7-13/h3-10,12,18-19H,11H2,1-2H3

InChI key: InChIKey=BPMLPIWGDJTUNN-UHFFFAOYSA-N

SMILES: C(C)(C)C1=C(B(O)O)C=CC(OCC2=CC=CC=C2)=C1

Synonyms:

• B-[2-(1-Methylethyl)-4-(phenylmethoxy)phenyl]boronic acid
• 4-Benzyloxy-2-isopropylbenzeneboronic acid
• (4-(Benzyloxy)-2-isopropylphenyl)boronic acid
• Boronic acid, B-[2-(1-methylethyl)-4-(phenylmethoxy)phenyl]-
• Boronic acid, [2-(1-methylethyl)-4-(phenylmethoxy)phenyl]-

Boronic acid, B-[2-(1-methylethyl)-4-(phenylmethoxy)phenyl]-

CAS: 211495-36-2

Formula: C₁₆H₁₉BO₃

Purity: 95%

Molecular weight: 270.1313

Ref: IN-DA01S1I0

4-Benzyloxy-2-isopropylphenylboronic acid

CAS: 211495-36-2

Purity: ≥95%

Molecular weight: 270.1400146

Ref: 10-F627755