(4-Isopropylphenyl)boronic Acid

• CAT Number: R063897
• CAS Number: 16152-51-5
• Molecular Formula: C9H13BO2
• Molecular Weight: 164.01
• Purity: ≥95%
• Synonyms: [4-(1-Methylethyl)phenyl]boronic Acid; p-Cumeneboronic Acid; 4-Isopropylbenzeneboronic Acid; 4-Isopropylphenylboronic Acid; [4-(1-Methylethyl)phenyl]boronic Acid; p-Isopropylphenylboronic Acid
• Storage: Store at -20°C
• IUPAC Name: (4-propan-2-ylphenyl)boronic acid
• InChI: InChI=1S/C9H13BO2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7,11-12H,1-2H3
• InChIKey: IAEUFBDMVKQCLU-UHFFFAOYSA-N
• SMILES: B(C1=CC=C(C=C1)C(C)C)(O)O

(4-Isopropylphenyl)boronic acid（Cat No.:R063897）is an arylboronic acid featuring a boronic acid group at the para position of an isopropyl-substituted phenyl ring. This compound is widely used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon–carbon bonds in the synthesis of biaryls, pharmaceuticals, and advanced materials. The isopropyl substituent offers steric and electronic modulation, enhancing selectivity and reactivity in catalytic processes. Known for its stability and compatibility with various reaction conditions, (4-isopropylphenyl)boronic acid is valuable in medicinal and organic synthesis.