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CAS 914635-99-7

:

2-Bromo-4,4,4-trifluoro-3-methylbutanoic acid

Description:
2-Bromo-4,4,4-trifluoro-3-methylbutanoic acid is an organic compound characterized by its unique structure, which includes a bromine atom and three fluorine atoms attached to a butanoic acid backbone. This compound features a branched alkyl chain with a methyl group at the third carbon position, contributing to its distinct properties. The presence of the trifluoromethyl group significantly influences its reactivity and polarity, making it a useful intermediate in organic synthesis and pharmaceuticals. The bromine substituent can also participate in nucleophilic substitution reactions, enhancing its utility in various chemical transformations. As a carboxylic acid, it exhibits acidic properties, allowing it to participate in acid-base reactions. The compound is likely to be soluble in polar solvents due to the presence of the carboxylic acid functional group, while the halogen substituents may affect its overall hydrophobicity. Safety and handling precautions should be observed, as halogenated compounds can pose environmental and health risks. Overall, 2-Bromo-4,4,4-trifluoro-3-methylbutanoic acid is a versatile compound with significant applications in synthetic chemistry.
Formula:C5H6BrF3O2
InChI:InChI=1S/C5H6BrF3O2/c1-2(5(7,8)9)3(6)4(10)11/h2-3H,1H3,(H,10,11)
InChI key:InChIKey=QTQIBOJDKKPPQG-UHFFFAOYSA-N
SMILES:C(C(C(O)=O)Br)(C(F)(F)F)C
Synonyms:
  • Butanoic acid, 2-bromo-4,4,4-trifluoro-3-methyl-
  • 2-Bromo-4,4,4-trifluoro-3-methylbutanoic acid
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