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Atomfair 1-Acetyl-4-bromo-5(3)-phenyl-3(5)-(trifluoromethyl)pyrazole C12H8BrF3N2O
Description 1-Acetyl-4-bromo-5(3)-phenyl-3(5)-(trifluoromethyl)pyrazole (CAS No. 231955-60-5) is a high-purity, specialized heterocyclic compound with the molecular formula C12H8BrF3N2O. Its IUPAC name is 1-[4-bromo-5-phenyl-3-(trifluoromethyl)pyrazol-1-yl]ethanone . This pyrazole derivative features a bromo-substituted phenyl ring and a trifluoromethyl group, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. The compound is rigorously tested for purity and stability, ensuring optimal performance in advanced applications. Suitable for researchers and scientists in medicinal chemistry, agrochemical development, and material science.
Description
Description
1-Acetyl-4-bromo-5(3)-phenyl-3(5)-(trifluoromethyl)pyrazole (CAS No. 231955-60-5) is a high-purity, specialized heterocyclic compound with the molecular formula C12H8BrF3N2O. Its IUPAC name is 1-[4-bromo-5-phenyl-3-(trifluoromethyl)pyrazol-1-yl]ethanone. This pyrazole derivative features a bromo-substituted phenyl ring and a trifluoromethyl group, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. The compound is rigorously tested for purity and stability, ensuring optimal performance in advanced applications. Suitable for researchers and scientists in medicinal chemistry, agrochemical development, and material science.
- CAS No: 231955-60-5
- Molecular Formula: C12H8BrF3N2O
- Molecular Weight: 333.10
- Exact Mass: 331.97721
- Monoisotopic Mass: 331.97721
- IUPAC Name: 1-[4-bromo-5-phenyl-3-(trifluoromethyl)pyrazol-1-yl]ethanone
- SMILES: CC(=O)N1C(=C(C(=N1)C(F)(F)F)Br)C2=CC=CC=C2
- Synonyms: 1-Acetyl-4-bromo-5(3)-phenyl-3(5)-(trifluoromethyl)pyrazole, 808764-25-2, 231955-60-5, 1-Acetyl-4-bromo-5-phenyl-3-(trifluoromethyl)pyrazole, 1-(4-Bromo-5-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)ethan-1-one
Application
This compound serves as a versatile building block in the synthesis of pharmaceuticals, particularly in the development of bioactive pyrazole derivatives. It is useful in cross-coupling reactions for creating novel trifluoromethyl-containing compounds. Researchers also employ it in agrochemical studies to explore potential pesticidal or herbicidal activity. Its unique structure enables applications in material science for designing functionalized polymers or ligands.
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