4-Amino-2-fluorobut-2-enoic acid, with the CAS number 113779-23-0, is an organic compound characterized by the presence of an amino group, a fluorine atom, and a double bond within its butenoic acid structure. This compound features a four-carbon backbone with a double bond between the second and third carbons, which contributes to its reactivity and potential applications in organic synthesis. The amino group (-NH2) is typically associated with basic properties, while the carboxylic acid group (-COOH) imparts acidic characteristics. The presence of the fluorine atom can enhance the compound's biological activity and influence its solubility and stability. 4-Amino-2-fluorobut-2-enoic acid may be of interest in pharmaceutical research and development due to its potential as a building block for more complex molecules or as a bioactive agent. Its unique structural features make it a subject of study in various fields, including medicinal chemistry and materials science.

4-amino-2-fluorobut-2-enoic acid

113779-23-0: (Z)-4-Amino-2-fluorobut-2-enoic acid, 4-Afbea, (2Z)-4-amino-2-fluorobut-2-enoic acid

2-Butenoic acid, 4-amino-2-fluoro-, (2Z)-

4-Amino-2-fluorobutanoic acid is a nature amino acid that has been shown to denature proteins. It acts as an acceptor in a nucleophilic attack with mercury(II) chloride, and can be activated by mercuric chloride. 4-Amino-2-fluorobutanoic acid also exhibits second order rate constants for the reaction of nucleophilic attack on chloride ions. The γ-aminobutyric acid (GABA) receptor is activated by 4-amino-2-fluorobutanoic acid, which leads to inhibition of the release of neurotransmitters, such as glutamate and dopamine. This may result in treatments for diseases such as epilepsy or Parkinson's disease.

CAS 113779-23-0: 4-amino-2-fluorobut-2-enoic acid

2-Butenoic acid, 4-amino-2-fluoro-, (2Z)-

Ref: IN-DA0009N4

4-Amino-2-Fluorobut-2-Enoic Acid

Ref: 3D-FA80499