The chemical substance known as (3S)-3-[[(1,1-Dimethylethoxy)carbonyl]amino]-4,4,4-trifluorobutanoic acid, with the CAS number 1310680-43-3, is an amino acid derivative characterized by the presence of a trifluorobutanoic acid moiety and a dimethylethoxycarbonyl group. This compound features a chiral center at the 3-position, which contributes to its stereochemistry and potential biological activity. The trifluoromethyl group enhances lipophilicity and may influence the compound's interaction with biological targets. The dimethylethoxycarbonyl group serves as a protective group for the amino functionality, which can be important in synthetic applications. This compound may exhibit unique properties such as increased stability and altered solubility compared to its non-fluorinated counterparts. Its structural features suggest potential applications in medicinal chemistry, particularly in the design of pharmaceuticals that target specific biological pathways. Overall, the combination of functional groups and stereochemistry makes this compound of interest for further research and development in various chemical and biological contexts.

(3S)-3-[[(1,1-Dimethylethoxy)carbonyl]amino]-4,4,4-trifluorobutanoic acid

1310680-43-3: The chemical substance known as (3S)-3-[[(1,1-Dimethylethoxy)carbonyl]amino]-4,4,4-trifluorobutanoic acid, with the CAS number 1310680-43-3, is an amino acid derivative characterized by the presence of a trifluorobutanoic acid moiety and a dimethylethoxycarbonyl group. This compound features a chiral center at the 3-position, which contributes to its stereochemistry and potential biological activity. The trifluoromethyl group enhances lipophilicity and may influence the compound's interaction with biological targets. The dimethylethoxycarbonyl group serves as a protective group for the amino functionality, which can be important in synthetic applications. This compound may exhibit unique properties such as increased stability and altered solubility compared to its non-fluorinated counterparts. Its structural features suggest potential applications in medicinal chemistry, particularly in the design of pharmaceuticals that target specific biological pathways. Overall, the combination of functional groups and stereochemistry makes this compound of interest for further research and development in various chemical and biological contexts.

CAS 1310680-43-3

(3S)-3-[[(1,1-Dimethylethoxy)carbonyl]amino]-4,4,4-trifluorobutanoic acid

(S)-Boc-3-amino-4,4,4-trifluorobutyric acid

Ref: 54-PC450009