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CAS 374-35-6

:

3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acid

Description:
3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acid, with the CAS number 374-35-6, is a fluorinated organic compound characterized by the presence of three fluorine atoms, a hydroxyl group, and a carboxylic acid functional group. This compound is a derivative of propanoic acid, featuring a tertiary carbon that is substituted with a hydroxyl group and three fluorine atoms, which significantly influence its chemical properties. The trifluoromethyl group enhances the acidity of the carboxylic acid, making it a stronger acid compared to non-fluorinated analogs. Additionally, the presence of the hydroxyl group contributes to its potential as a hydrogen bond donor, affecting its solubility and reactivity in various solvents. The compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its unique properties and potential applications. Its stability and reactivity can be influenced by the presence of the electronegative fluorine atoms, which can also affect its interactions with biological systems.
Formula:C4H5F3O3
InChI:InChI=1S/C4H5F3O3/c1-3(10,2(8)9)4(5,6)7/h10H,1H3,(H,8,9)
InChI key:InChIKey=CTGJACFEVDCYMC-UHFFFAOYSA-N
SMILES:C(C(F)(F)F)(C(O)=O)(C)O
Synonyms:
  • 2-(Trifluoromethyl)-2-hydroxypropanoic acid
  • 2-(Trifluoromethyl)lactic acid
  • 2-Hydroxy-2-(trifluoromethyl)propanoic acid
  • 2-Hydroxy-2-(trifluoromethyl)propionic acid
  • 2-Hydroxy-2-methyl-3,3,3-trifluoropropanoic acid
  • 2-Trifluoromethyl-2-Hydroxypropionic Acid
  • 3,3,3-Trifluoro-2-Hydroxy-2-Methylpropanoic Acid
  • Propanoic acid, 3,3,3-trifluoro-2-hydroxy-2-methyl-
  • α-(Trifluoromethyl)lactic acid
  • α-Methyl-3,3,3-trifluorolactic acid
  • 3,3,3-Trifluoro-2-hydroxy-2-methylpropionic acid
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