Description

1-(3-Bromophenyl)ethanol (CAS No. 52780-14-0) is a high-purity brominated aromatic alcohol with the molecular formula C₈H₉BrO. This compound is a valuable intermediate in organic synthesis and pharmaceutical research, featuring a hydroxyl group and a bromine substituent on the phenyl ring, which enhances its reactivity in coupling reactions and functional group transformations. Ideal for use in Suzuki-Miyaura cross-coupling, Grignard reactions, and as a chiral building block in asymmetric synthesis. Our product is rigorously tested for purity (typically ≥95% by GC/HPLC) and is supplied in sealed containers under inert gas to ensure stability. Suitable for researchers in medicinal chemistry, material science, and fine chemical production.

Properties

• CAS Number: 52780-14-0
• Complexity: 105
• IUPAC Name: 1-(3-bromophenyl)ethanol
• InChI: InChI=1S/C8H9BrO/c1-6(10)7-3-2-4-8(9)5-7/h2-6,10H,1H3
• InChI Key: ULMJQMDYAOJNCC-UHFFFAOYSA-N
• Exact Mass: 199.98368
• Molecular Formula: C8H9BrO
• Molecular Weight: 201.06
• SMILES: CC(C1=CC(=CC=C1)Br)O
• Topological: 20.2
• Monoisotopic Mass: 199.98368
• Synonyms: 1-(3-bromophenyl)ethanol, 52780-14-0, DTXSID001312987, DTXCID60895090, 3-Bromo-alpha-methylbenzyl alcohol, 1-(3-bromophenyl)ethan-1-ol, 3-Bromo-alpha-methylbenzene alcohol, MFCD00021863, 3-Bromophenyl methyl carbinol, 1-(3′-bromophenyl)-1-hydroxyethane, 3-Bromo-A-methylbenzyl alcohol, MFCD06201859, MFCD06658929, EINECS 258-177-7, NSC143363, 3-bromophenyl-ethanol, 1-(3-bromophenyl)-ethanol, 1-(3-bromo-phenyl)-ethanol, SCHEMBL343476, SCHEMBL1044626, m-bromo-alpha-methylbenzylalcohol, SCHEMBL16962938, SCHEMBL20764854, 3-Bromo- alpha -methylbenzyl alcohol, AKOS000125402, NSC 143363, NSC-143363, 3-Bromo-alpha-methylbenzyl alcohol, 97%, Benzenemethanol, 3-bromo-.alpha.-methyl-, CS-11083, DA-21165, SY005048, SY104344, SY107032, DB-052185, CS-0154116, NS00058775, ST51041413, EN300-131312, A829250

Application

1-(3-Bromophenyl)ethanol is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and liquid crystals. Its bromine moiety enables participation in palladium-catalyzed cross-coupling reactions, while the hydroxyl group allows for further derivatization. This compound is particularly valuable in the development of chiral ligands and catalysts. It also serves as a precursor for bioactive molecules in drug discovery programs.

Safety and Hazards

GHS Hazard Statements

• H226 (97.6%): Flammable liquid and vapor [Warning Flammable liquids]

Precautionary Statements

• P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501

Hazard Classes and Categories

• Flam. Liq. 3 (97.6%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.