The chemical substance with the name "(αS,3S)-1-[(1,1-Dimethylethoxy)carbonyl]-α-[[[9H-fluoren-9-ylmethoxy]carbonyl]amino]-3-piperidinepropanoic acid" and CAS number "1251903-97-5" is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a piperidine ring, which contributes to its cyclic structure and potential biological activity. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates its use in peptide synthesis, particularly as a protecting group for amino acids. The dimethylethoxycarbonyl moiety suggests that it may also serve as a protective group for the carboxylic acid functionality. This compound is likely to be soluble in organic solvents due to its hydrophobic groups, while the carboxylic acid may impart some degree of polarity. Its structural complexity and specific stereochemistry may influence its reactivity and interactions in biological systems, making it of interest in medicinal chemistry and drug development. Overall, this compound exemplifies the intricate design often found in synthetic organic chemistry, particularly in the context of peptide synthesis and modification.

(αS,3S)-1-[(1,1-Dimethylethoxy)carbonyl]-α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-3-piperidinepropanoic acid

1251903-97-5: The chemical substance with the name "(αS,3S)-1-[(1,1-Dimethylethoxy)carbonyl]-α-[[[9H-fluoren-9-ylmethoxy]carbonyl]amino]-3-piperidinepropanoic acid" and CAS number "1251903-97-5" is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a piperidine ring, which contributes to its cyclic structure and potential biological activity. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates its use in peptide synthesis, particularly as a protecting group for amino acids. The dimethylethoxycarbonyl moiety suggests that it may also serve as a protective group for the carboxylic acid functionality. This compound is likely to be soluble in organic solvents due to its hydrophobic groups, while the carboxylic acid may impart some degree of polarity. Its structural complexity and specific stereochemistry may influence its reactivity and interactions in biological systems, making it of interest in medicinal chemistry and drug development. Overall, this compound exemplifies the intricate design often found in synthetic organic chemistry, particularly in the context of peptide synthesis and modification.

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((S)-1-(tert-butoxycarbonyl)piperidin-3-yl)propanoic acid

CAS 1251903-97-5

(αS,3S)-1-[(1,1-Dimethylethoxy)carbonyl]-α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-3-piperidinepropanoic acid

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((S)-1-(tert-butoxycarbonyl)piperidin-3-yl)propanoic acid

Ref: 54-OR1051038