Description

2-Bromo-5-fluorobenzyl alcohol (CAS No. 202865-66-5) is a high-purity fluorinated benzyl alcohol derivative, widely utilized as a key intermediate in pharmaceutical synthesis and advanced organic chemistry research. This compound, with the molecular formula C₇H₆BrFO, features a bromo-fluoro substitution pattern that enhances its reactivity in cross-coupling reactions, nucleophilic substitutions, and as a building block for bioactive molecules. Our product is rigorously tested to ensure ≥97% purity (GC), making it ideal for demanding applications in medicinal chemistry, agrochemical development, and material science. Supplied in sealed packaging under inert conditions to guarantee stability and longevity.

Key Features:

• High chemical purity (≥97%) for precision reactions
• Versatile electrophilic properties for diverse synthetic pathways
• Stable under standard storage conditions
• Compatible with palladium-catalyzed coupling reactions
• Available in research quantities with bulk options

Properties

• CAS Number: 202865-66-5
• Complexity: 110
• IUPAC Name: (2-bromo-5-fluoro-phenyl)methanol
• InChI: InChI=1S/C7H6BrFO/c8-7-2-1-6(9)3-5(7)4-10/h1-3,10H,4H2
• InChI Key: HXGZPMHPSBJMKB-UHFFFAOYSA-N
• Exact Mass: 203.95861
• Molecular Formula: C7H6BrFO
• Molecular Weight: 205.02
• SMILES: C1=CC(=C(C=C1F)CO)Br
• Topological: 20.2
• Monoisotopic Mass: 203.95861
• Synonyms: 2-Bromo-5-fluorobenzyl alcohol, 202865-66-5, DTXSID00378397, DTXCID40329424, 606-492-9, (2-bromo-5-fluorophenyl)methanol, 2-bromo-5-fluorobenzylalcohol, BENZENEMETHANOL, 2-BROMO-5-FLUORO-, MFCD00142876, (2-bromo-5-fluorophenyl)methan-1-ol, Bromo-5-fluorobenzyl alcohol, SCHEMBL458270, SCHEMBL5430076, SCHEMBL16958007, (2-bromo-5-fluoro-phenyl)methanol, (2-bromo-5-fluorophenyl)-methanol, (2- bromo-5-fluoro-phenyl)methanol, (2-bromo-5-fluoro-phenyl)-methanol, SBB063440, AKOS005257312, 2-Bromo-5-fluorobenzyl alcohol, 97%, AC-2309, CS-W008302, DS-0989, FB64448, PS-8130, (2-bromanyl-5-fluoranyl-phenyl)methanol, SY014474, ST51041795, EN300-155933, A802341

This fluorinated benzyl alcohol serves as a crucial precursor in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions for pharmaceutical intermediates. Researchers employ it in developing kinase inhibitors and PET radiotracer candidates due to its balanced lipophilicity and metabolic stability. The bromo-fluoro substitution pattern enables selective functionalization in complex molecule synthesis.

Safety and Hazards

GHS Hazard Statements

• H302 (97.7%): Harmful if swallowed [Warning Acute toxicity, oral]
• H319 (95.5%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

Precautionary Statements

• P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P330, P337+P317, and P501

Hazard Classes and Categories

• Acute Tox. 4 (97.7%)
• Eye Irrit. 2A (95.5%)

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