CAS 381-97-5

Propanoic acid, 3,3,3-trifluoro-2-methyl-

Description:

Propanoic acid, 3,3,3-trifluoro-2-methyl- is a fluorinated carboxylic acid characterized by the presence of a propanoic acid backbone with a trifluoromethyl group and a methyl group attached to the second carbon. This compound features a molecular structure that includes three fluorine atoms, which significantly influence its chemical properties, such as increased acidity and altered reactivity compared to non-fluorinated analogs. The presence of the trifluoromethyl group enhances its lipophilicity and can affect its solubility in various solvents. Additionally, the compound exhibits typical carboxylic acid characteristics, including the ability to form hydrogen bonds, which can impact its boiling and melting points. Its unique structure makes it of interest in various applications, including pharmaceuticals and agrochemicals, where fluorinated compounds often exhibit enhanced biological activity or stability. Safety considerations should be taken into account due to the potential toxicity associated with fluorinated compounds.

Formula: C₄H₅F₃O₂

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

CAS: 381-97-5

Formula: C₄H₅F₃O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 142.0765

Ref: IN-DA00CIU6

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

CAS: 381-97-5

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

Formula: C₄H₅F₃O₂

Purity: 97%

Color and Shape: clear liquid

Molecular weight: 142.08g/mol

Ref: 54-PC201243

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

CAS: 381-97-5

Formula: C₄H₅F₃O₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 142.077

Ref: 10-F221062

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

CAS: 381-97-5

3,3,3-Trifluoro-2-methylpropanoic acid is a racemic mixture of 3,3,3-trifluoro-2-methylpropanoic acid and its enantiomer. It is an organic compound that is used as a reagent in organic synthesis. It has the property of being hydrolyzed by lipase mediated by hydrolytic enzymes to form 3,3,3-trifluoroethanol and propanoic acid. The enantiomers are racemic mixtures of 3,3,3-trifluoropropionic acid and (R)-(+)-3,3,3-trifluoropropionic acid. Both enantiomers have the same chemical properties but their kinetic behavior differs because one is a substrate for lipase while the other is not.

Formula: C₄H₅F₃O₂

Purity: Min. 95%

Molecular weight: 142.08 g/mol

Ref: 3D-AAA38197