The chemical substance known as (2S)-3-(tert-butoxy)-2-[(2S)-3-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid, with the CAS number 110098-50-5, is a complex organic compound characterized by its multi-functional structure. It features a tert-butoxy group, which contributes to its hydrophobic properties, and a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect amino groups. The presence of multiple chiral centers indicates that the compound exists in specific stereoisomeric forms, which can significantly influence its biological activity and interactions. This compound is likely to be soluble in organic solvents due to its hydrophobic components, while its polar functional groups may enhance solubility in polar solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of peptide-based therapeutics. The stability and reactivity of the compound can be influenced by the presence of the tert-butoxy and Fmoc groups, making it a valuable intermediate in synthetic organic chemistry.

(2S)-3-(tert-butoxy)-2-[(2S)-3-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid

110098-50-5: The chemical substance known as (2S)-3-(tert-butoxy)-2-[(2S)-3-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid, with the CAS number 110098-50-5, is a complex organic compound characterized by its multi-functional structure. It features a tert-butoxy group, which contributes to its hydrophobic properties, and a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect amino groups. The presence of multiple chiral centers indicates that the compound exists in specific stereoisomeric forms, which can significantly influence its biological activity and interactions. This compound is likely to be soluble in organic solvents due to its hydrophobic components, while its polar functional groups may enhance solubility in polar solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of peptide-based therapeutics. The stability and reactivity of the compound can be influenced by the presence of the tert-butoxy and Fmoc groups, making it a valuable intermediate in synthetic organic chemistry.

N-(N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-(tert-butyl)-L-seryl)-O-(tert-butyl)-L-serine

CAS 110098-50-5

(2S)-3-(tert-butoxy)-2-[(2S)-3-(tert-butoxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid

N-(N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-(tert-butyl)-L-seryl)-O-(tert-butyl)-L-serine

Ref: 54-OR1071837