The chemical substance known as (2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-{[(4-methylphenyl)methyl]selanyl}propanoic acid, with the CAS number 1365284-49-6, is a complex organic compound characterized by its unique structural features. It contains a propanoic acid backbone, which is modified with a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect amino groups. The presence of a selenium atom in the side chain, specifically as a selenyl group attached to a 4-methylphenylmethyl moiety, indicates potential applications in medicinal chemistry, particularly in the development of organoselenium compounds known for their biological activity. The stereochemistry at the 2-position (2R) suggests that the compound exhibits chirality, which can influence its reactivity and interaction with biological systems. Overall, this compound's intricate structure and functional groups may contribute to its potential utility in various chemical and pharmaceutical applications, particularly in the synthesis of novel bioactive molecules.

(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-{[(4-methylphenyl)methyl]selanyl}propanoic acid

1365284-49-6: The chemical substance known as (2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-{[(4-methylphenyl)methyl]selanyl}propanoic acid, with the CAS number 1365284-49-6, is a complex organic compound characterized by its unique structural features. It contains a propanoic acid backbone, which is modified with a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect amino groups. The presence of a selenium atom in the side chain, specifically as a selenyl group attached to a 4-methylphenylmethyl moiety, indicates potential applications in medicinal chemistry, particularly in the development of organoselenium compounds known for their biological activity. The stereochemistry at the 2-position (2R) suggests that the compound exhibits chirality, which can influence its reactivity and interaction with biological systems. Overall, this compound's intricate structure and functional groups may contribute to its potential utility in various chemical and pharmaceutical applications, particularly in the synthesis of novel bioactive molecules.

Fmoc-Sec(pMeBzl)-OH

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((4-methylbenzyl)selanyl)propanoic acid

CAS 1365284-49-6

(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-{[(4-methylphenyl)methyl]selanyl}propanoic acid

Fmoc-Sec(pMeBzl)-OH

Ref: IN-DA01K24V

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((4-methylbenzyl)selanyl)propanoic acid

Ref: 54-OR1057869