Atomfair 4-Bromo-3-nitrobenzotrifluoride C7H3BrF3NO2

Description 4-Bromo-3-nitrobenzotrifluoride (CAS No. 349-03-1) is a high-purity aromatic compound with the molecular formula C7H3BrF3NO2and IUPAC name 1-bromo-2-nitro-4-(trifluoromethyl)benzene . This halogenated nitrobenzene derivative features a bromo substituent at the 4-position and a nitro group at the 3-position relative to the electron-withdrawing trifluoromethyl group, making it a valuable intermediate in synthetic organic chemistry. The compound is supplied as a crystalline solid with >98% purity (HPLC) and is rigorously tested for consistency in reactivity. Ideal for use in cross-coupling reactions, nucleophilic substitutions, and as a building block for pharmaceuticals, agrochemicals, and advanced materials. Packaged under inert gas to ensure stability, with detailed…

Description

4-Bromo-3-nitrobenzotrifluoride (CAS No. 349-03-1) is a high-purity aromatic compound with the molecular formula C₇H₃BrF₃NO₂ and IUPAC name 1-bromo-2-nitro-4-(trifluoromethyl)benzene. This halogenated nitrobenzene derivative features a bromo substituent at the 4-position and a nitro group at the 3-position relative to the electron-withdrawing trifluoromethyl group, making it a valuable intermediate in synthetic organic chemistry. The compound is supplied as a crystalline solid with >98% purity (HPLC) and is rigorously tested for consistency in reactivity. Ideal for use in cross-coupling reactions, nucleophilic substitutions, and as a building block for pharmaceuticals, agrochemicals, and advanced materials. Packaged under inert gas to ensure stability, with detailed technical data (MSDS, NMR, HPLC) available upon request.

CAS No: 349-03-1
Molecular Formula: C7H3BrF3NO2
Molecular Weight: 270.00
Exact Mass: 268.92993
Monoisotopic Mass: 268.92993
IUPAC Name: 1-bromo-2-nitro-4-(trifluoromethyl)benzene
SMILES: C1=CC(=C(C=C1C(F)(F)F)[N+](=O)[O-])Br
Synonyms: 4-Bromo-3-nitrobenzotrifluoride, 349-03-1, DTXSID60334434, DTXCID70285524, 670-406-6

Application

4-Bromo-3-nitrobenzotrifluoride serves as a versatile intermediate in the synthesis of trifluoromethyl-substituted aromatic compounds, particularly in pharmaceutical research for developing kinase inhibitors and antimicrobial agents. Its electron-deficient aromatic ring facilitates Suzuki-Miyaura and Buchwald-Hartwig coupling reactions to construct complex heterocycles. The compound is also employed in agrochemical production for creating herbicides with enhanced bioavailability due to the lipophilic trifluoromethyl group.

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