Description

3,5-Bis(trifluoromethyl)benzyl bromide (CAS No. 32247-96-4) is a highly versatile and reactive organofluorine compound with the molecular formula C₉H₅BrF₆. This aromatic bromide is characterized by the presence of two trifluoromethyl groups at the 3 and 5 positions of the benzene ring, along with a reactive bromomethyl group at the 1 position. Its IUPAC name is 1-(bromomethyl)-3,5-bis(trifluoromethyl)benzene.

This compound is widely utilized in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and advanced materials. Its electron-withdrawing trifluoromethyl groups enhance its reactivity, making it an excellent building block for nucleophilic substitution reactions, cross-coupling reactions, and as a precursor for ligands or catalysts.

Our product is rigorously tested for purity and stability, ensuring optimal performance in demanding research and industrial applications. It is supplied in high-quality packaging to maintain integrity and shelf life.

Properties

• CAS Number: 32247-96-4
• Complexity: 211
• IUPAC Name: 1-(bromomethyl)-3,5-bis(trifluoromethyl)benzene
• InChI: InChI=1S/C9H5BrF6/c10-4-5-1-6(8(11,12)13)3-7(2-5)9(14,15)16/h1-3H,4H2
• InChI Key: ATLQGZVLWOURFU-UHFFFAOYSA-N
• Exact Mass: 305.94788
• Molecular Formula: C9H5BrF6
• Molecular Weight: 307.03
• SMILES: C1=C(C=C(C=C1C(F)(F)F)C(F)(F)F)CBr
• Monoisotopic Mass: 305.94788
• Synonyms: 3,5-Bis(trifluoromethyl)benzyl bromide, 1-(Bromomethyl)-3,5-bis(trifluoromethyl)benzene, 3,5-di(Trifluoromethyl)benzyl bromide, 3,5-bis(trifluoromethyl)benzylbromide, Benzene, 1-(bromomethyl)-3,5-bis(trifluoromethyl)-, EINECS 250-971-1, ATLQGZVLWOURFU-UHFFFAOYSA-, DTXSID10186001, BTFMBzBr, DTXCID80108492, 250-971-1, atlqgzvlwourfu-uhfffaoysa-n, inchi=1/c9h5brf6/c10-4-5-1-6(8(11,12)13)3-7(2-5)9(14,15)16/h1-3h,4h2, 32247-96-4, MFCD00009905, 1-Bromomethyl-3,5-bis(trifluoromethyl)benzene, 1,3-bis(trifluoromethyl)-5-(bromomethyl)benzene, alpha”-Bromo-alpha,alpha,alpha,alpha’,alpha’,alpha’-hexafluoro-mesitylene; 1-(Bromomethyl)-3,5-bis(trifluoromethyl)benzene; 1-Bromomethyl-3,5-ditrifluoromethylbenzene; 3,5-(Trifluoromethyl)benzyl Bromide; 3,5-Di(trifluoromethyl)benzyl Bromide, 3,5-bis-(Trifluoromethyl)benzyl bromide, SCHEMBL107565, BCP27529, 3,5-bistrifluoromethylbenzyl bromide, 3,5-Bis(trifluromethyl)benzylbromide, 3,5-bis-trifluoromethybenzyl bromide, SBB070955, 3,5 bis(trifluoromethyl)benzylbromide, 3,5-bis trifluoromethyl benzylbromide, 3,5-bis-trifluoromethyl-benzylbromide, 3,5-bis-trifluoromethylbenzyl bromide, 3.5-bis(trifluormethyl)-benzylbromide, AKOS015852932, 3,5-bis trifluoromethyl benzyl bromide, 3,5-bis-trifluoromethyl-benzyl bromide, AC-4154, 3,5-di-(trifluoromethyl)benzyl bromide, 3,5-B is(trifluoromethyl)benzyl bromide, 3,5-bis(trifluoromethyl) benzyl bromide, 3,5-bis (trifluoromethyl)-benzyl bromide, AS-11019, DB-001247, B1867, NS00059260, 1-Bromomethyl-3,5-bis-trifluoromethyl-benzene, 3,5-Bis(trifluoromethyl)benzyl bromide, 97%, 1-bromo methyl-3,5-bis(trifluoromethyl)benzene, 1-bromomethyl-3,5-bis(trifluoromethyl)-benzene, B49500, EN300-310365, 1-(Bromomethyl)-3,5-bis(trifluoromethyl)benzene #, Q63391925, 6-Chloro-4,5-pyrimidinediamine;6-Chloro-4,5-diaminopyrimidine;6-Chloropyrimidine-4,5-diamine

Application

3,5-Bis(trifluoromethyl)benzyl bromide is commonly employed as a key intermediate in the synthesis of biologically active molecules, including pharmaceuticals and agrochemicals. Its reactive benzyl bromide moiety allows for facile functionalization, making it valuable in cross-coupling reactions and the construction of complex organic frameworks. Additionally, it serves as a precursor for ligands in catalysis and as a building block in materials science for designing fluorinated polymers or liquid crystals.

Safety and Hazards

GHS Hazard Statements

• H226 (93%): Flammable liquid and vapor [Warning Flammable liquids]
• H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]

Precautionary Statements

• P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P321, P363, P370+P378, P403+P235, P405, and P501

Hazard Classes and Categories

• Flam. Liq. 3 (93%)
• Skin Corr. 1B (100%)

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