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Atomfair 4-Isopropylphenylboronic acid C9H13BO2
Description 4-Isopropylphenylboronic acid (CAS No. 153624-46-5) is a high-purity boronic acid derivative with the molecular formula C9H13BO2and IUPAC name (4-propan-2-ylphenyl)boronic acid . This organoboron compound is a versatile building block in synthetic organic chemistry, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for the construction of biaryl and heteroaryl structures. Its isopropyl-substituted phenyl ring enhances steric and electronic properties, making it valuable in pharmaceutical, agrochemical, and materials science research. Available in crystalline powder form, our product is rigorously tested for purity (typically ??95-98% by HPLC or NMR) and is packaged under inert conditions to ensure stability.…
Description
Description
4-Isopropylphenylboronic acid (CAS No. 153624-46-5) is a high-purity boronic acid derivative with the molecular formula C9H13BO2 and IUPAC name (4-propan-2-ylphenyl)boronic acid. This organoboron compound is a versatile building block in synthetic organic chemistry, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for the construction of biaryl and heteroaryl structures. Its isopropyl-substituted phenyl ring enhances steric and electronic properties, making it valuable in pharmaceutical, agrochemical, and materials science research. Available in crystalline powder form, our product is rigorously tested for purity (typically ??95-98% by HPLC or NMR) and is packaged under inert conditions to ensure stability. Suitable for use in catalysis, ligand design, and medicinal chemistry applications.
- CAS No: 153624-46-5
- Molecular Formula: C9H13BO2
- Molecular Weight: 164.01
- Exact Mass: 164.1008598
- Monoisotopic Mass: 164.1008598
- IUPAC Name: (4-propan-2-ylphenyl)boronic acid
- SMILES: B(C1=CC=C(C=C1)C(C)C)(O)O
- Synonyms: 4-Isopropylphenylboronic acid, 16152-51-5, DTXSID70378485, DTXCID10329512, 678-567-4
Application
4-Isopropylphenylboronic acid is widely used as a reagent in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, including pharmaceuticals and liquid crystals. Its steric profile facilitates selective coupling in the presence of sensitive functional groups. Researchers also employ it in the development of boron-based sensors and as a precursor for covalent organic frameworks (COFs).
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