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Atomfair 3,5-Difluorobenzyl bromide C7H5BrF2
Description 3,5-Difluorobenzyl bromide (CAS 141776-91-2) is a high-purity aromatic bromide compound with the molecular formula C7H5BrF2. This organofluorine building block features a reactive benzyl bromide group flanked by two fluorine atoms at the 3- and 5-positions, making it an excellent electrophile for nucleophilic substitution reactions. The compound is supplied as a clear to pale yellow liquid with typical purity >95% (GC), packaged under inert gas to prevent degradation. Ideal for pharmaceutical intermediates, agrochemical synthesis, and materials science applications requiring selective fluorination. Proper storage at 2-8??C in amber vials is recommended to maintain stability. Hazard classification includes skin/eye irritant and moisture-sensitive…
Description
Description
3,5-Difluorobenzyl bromide (CAS 141776-91-2) is a high-purity aromatic bromide compound with the molecular formula C7H5BrF2. This organofluorine building block features a reactive benzyl bromide group flanked by two fluorine atoms at the 3- and 5-positions, making it an excellent electrophile for nucleophilic substitution reactions. The compound is supplied as a clear to pale yellow liquid with typical purity >95% (GC), packaged under inert gas to prevent degradation. Ideal for pharmaceutical intermediates, agrochemical synthesis, and materials science applications requiring selective fluorination. Proper storage at 2-8??C in amber vials is recommended to maintain stability. Hazard classification includes skin/eye irritant and moisture-sensitive properties – handle with appropriate PPE in a fume hood.
- CAS No: 141776-91-2
- Molecular Formula: C7H5BrF2
- Molecular Weight: 207.01
- Exact Mass: 205.95427
- Monoisotopic Mass: 205.95427
- IUPAC Name: 1-(bromomethyl)-3,5-difluorobenzene
- SMILES: C1=C(C=C(C=C1F)F)CBr
- Synonyms: 3,5-Difluorobenzyl bromide, 141776-91-2, DTXSID40333844, DTXCID50284934, 627-819-1
Application
3,5-Difluorobenzyl bromide serves as a key synthetic intermediate for introducing difluorobenzyl motifs in medicinal chemistry. The compound is particularly valuable in the development of kinase inhibitors and CNS-active pharmaceuticals where fluorine substitution modulates bioavailability. In material science, it acts as a precursor for liquid crystals and fluorinated polymers. The reactive benzyl bromide group enables facile coupling reactions in Pd-catalyzed cross-couplings or nucleophilic substitutions.
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