Atomfair 3-Fluorobenzyl bromide C7H6BrF CAS 456-41-7

3-Fluorobenzyl Bromide (CAS No. 456-41-7) is a highly versatile halogenated aromatic compound with the molecular formula C7H6BrF. This organic intermediate features a benzyl bromide group substituted with a fluorine atom at the meta position, making it a valuable building block in synthetic organic chemistry, pharmaceutical research, and material science applications. With a purity of 99%, this reagent is ideal for nucleophilic substitution reactions, cross-coupling reactions, and as a precursor for further functionalization. Packaged under strict quality control, our 3-Fluorobenzyl Bromide ensures consistent performance in laboratory and industrial settings. Store in a cool, dry place away from light and moisture to…

Description

3-Fluorobenzyl Bromide (CAS No. 456-41-7) is a highly versatile halogenated aromatic compound with the molecular formula C7H6BrF. This organic intermediate features a benzyl bromide group substituted with a fluorine atom at the meta position, making it a valuable building block in synthetic organic chemistry, pharmaceutical research, and material science applications. With a purity of 99%, this reagent is ideal for nucleophilic substitution reactions, cross-coupling reactions, and as a precursor for further functionalization. Packaged under strict quality control, our 3-Fluorobenzyl Bromide ensures consistent performance in laboratory and industrial settings. Store in a cool, dry place away from light and moisture to maintain stability.

Properties

  • CAS Number: 456-41-7
  • Complexity: 85
  • IUPAC Name: 1-(bromomethyl)-3-fluoro-benzene
  • InChI: InChI=1S/C7H6BrF/c8-5-6-2-1-3-7(9)4-6/h1-4H,5H2
  • InChI Key: SCBZBMXPJYMXRC-UHFFFAOYSA-N
  • Exact Mass: 187.96369
  • Molecular Formula: C7H6BrF
  • Molecular Weight: 189.02
  • SMILES: C1=CC(=CC(=C1)F)CBr
  • Monoisotopic Mass: 187.96369
  • Synonyms: 3-Fluorobenzyl bromide, 456-41-7, Benzene, 1-(bromomethyl)-3-fluoro-, alpha-Bromo-3-fluorotoluene, meta-Fluorobenzyl bromide, EINECS 207-263-2, NSC 91494, .alpha.-Bromo-3-fluorotoluene, DTXSID9060025, DTXCID3040437, scbzbmxpjymxrc-uhfffaoysa-n, 1-(Bromomethyl)-3-fluorobenzene, 3-fluorobenzylbromide, m-fluorobenzyl bromide, m-Fluorobenzylbromide, Toluene, .alpha.-bromo-m-fluoro-, alpha-Bromo-m-fluorotoluene, 3-(bromomethyl)-1-fluorobenzene, 1-(Bromomethyl)-3-fluorobenzene; m-Fluorobenzyl Bromide; a-Bromo-3-fluorotoluene; a-Bromo-m-fluorotoluene; NSC 91494;, NSC91494, MFCD00000340, 3-fluoro benzylbromide, 3-fluorobenzyl-bromide, 3-Fluoro-benzylbromide, 3-fluoro benzyl bromide, 3-fluoro-benzyl bromide, a-Bromo-3-fluorotoluene, 3-fluorophenylmethyl bromide, SCHEMBL3830, 1-bromomethyl-3-fluorobenzene, 3-Fluorobenzyl bromide, 99%, 1-bromomethyl-3-fluoro-benzene, Toluene, alpha-bromo-m-fluoro-, SCHEMBL28740379, 1-(Bromomethyl)-3-fluorobenzene #, NSC-91494, SBB090883, AKOS005259838, FF38630, PB42853, AS-10896, DB-024084, CS-0005783, F0208, NS00044067, ST51039959, EN300-22614, D78091, F0001-1237

3-Fluorobenzyl Bromide is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a versatile alkylating agent in organic synthesis, particularly in the preparation of fluorinated aromatic compounds. Researchers utilize this compound in cross-coupling reactions to create complex molecular architectures for drug discovery. Its reactivity makes it suitable for modifying polymers and creating advanced materials with tailored properties.

Safety and Hazards

GHS Hazard Statements

  • H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
  • H335 (78.8%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

  • P260, P261, P264, P271, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P319, P321, P363, P403+P233, P405, and P501

Hazard Classes and Categories

  • Skin Corr. 1B (100%)
  • STOT SE 3 (78.8%)

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

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