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Atomfair 1-Bromo-3-(trifluoromethoxy)benzene C7H4BrF3O
Description 1-Bromo-3-(trifluoromethoxy)benzene (CAS No. 2252-44-0) is a high-purity aromatic compound with the molecular formula C7H4BrF3O . This specialized chemical features a benzene ring substituted with a bromine atom and a trifluoromethoxy group at the meta position, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure offers excellent reactivity for cross-coupling reactions, nucleophilic substitutions, and as a precursor for advanced fluorinated materials. Suitable for use in HPLC, GC-MS, and NMR applications, this compound is rigorously tested to ensure ??98% purity (GC). Packaged under inert gas to maintain stability, it is ideal for researchers requiring precise and…
Description
Description
1-Bromo-3-(trifluoromethoxy)benzene (CAS No. 2252-44-0) is a high-purity aromatic compound with the molecular formula C7H4BrF3O. This specialized chemical features a benzene ring substituted with a bromine atom and a trifluoromethoxy group at the meta position, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure offers excellent reactivity for cross-coupling reactions, nucleophilic substitutions, and as a precursor for advanced fluorinated materials. Suitable for use in HPLC, GC-MS, and NMR applications, this compound is rigorously tested to ensure ??98% purity (GC). Packaged under inert gas to maintain stability, it is ideal for researchers requiring precise and reliable building blocks for complex molecular architectures.
- CAS No: 2252-44-0
- Molecular Formula: C7H4BrF3O
- Molecular Weight: 241.00
- Exact Mass: 239.93976
- Monoisotopic Mass: 239.93976
- IUPAC Name: 1-bromo-3-(trifluoromethoxy)benzene
- SMILES: C1=CC(=CC(=C1)Br)OC(F)(F)F
- Synonyms: 1-Bromo-3-(trifluoromethoxy)benzene, 2252-44-0, BENZENE, 1-BROMO-3-(TRIFLUOROMETHOXY)-, DTXSID90334205, DTXCID60285295
Application
1-Bromo-3-(trifluoromethoxy)benzene is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and liquid crystals. Its trifluoromethoxy group enhances metabolic stability and lipophilicity in drug design, making it valuable for medicinal chemistry. This compound is also employed in material science for developing fluorinated polymers and advanced electronic materials. Researchers utilize it in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions to construct complex aromatic systems.
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