CAS 181128-48-3

Butanoic acid,2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4,4,4-trifluoro-, (S)-

Description:

Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4,4,4-trifluoro-, (S)-, is a chemical compound characterized by its unique structure that includes a butanoic acid moiety, a fluorenylmethoxycarbonyl (Fmoc) protecting group, and trifluoromethyl substituents. The presence of the Fmoc group indicates its use in peptide synthesis, where it serves as a protective group for amino acids. The trifluoromethyl groups enhance the compound's lipophilicity and can influence its biological activity and interaction with other molecules. This compound is typically used in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its stereochemistry is specified as (S), indicating the configuration around the chiral center, which is crucial for its biological function. The compound is likely to exhibit moderate solubility in organic solvents and may have specific reactivity patterns due to the functional groups present. Overall, its unique characteristics make it a valuable compound in synthetic organic chemistry and drug development.

Formula: C₁₉H₁₆F₃NO₄

Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4,4,4-trifluoro-, (2S)-

CAS: 181128-48-3

Formula: C₁₉H₁₆F₃NO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 379.3298

Ref: IN-DA0022OX

(L)-4,4,4,-Trifluoro-α-homoalanine, N-FMOC protected

CAS: 181128-48-3

(L)-4,4,4,-Trifluoro-α-homoalanine, N-FMOC protected

Purity: 98%

Molecular weight: 379.33g/mol

Ref: 54-PC5242

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4,4,4-trifluorobutanoic acid

CAS: 181128-48-3

Formula: C₁₉H₁₆F₃NO₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 379.335

Ref: 10-F446120