The chemical substance known as (2R)-2-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid, with the CAS number 538334-18-8, is a synthetic amino acid derivative. It features a complex structure that includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect amino groups during the formation of peptide bonds. This compound exhibits characteristics typical of amino acids, such as the presence of both an amine and a carboxylic acid functional group, allowing it to participate in various chemical reactions, including peptide bond formation. The stereochemistry indicated by the (2R) and (2S) designations suggests specific spatial arrangements of the atoms, which can influence the compound's biological activity and interactions. Additionally, the presence of the fluorenyl group may enhance the compound's stability and solubility in organic solvents. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis, where it may serve as an intermediate or building block for more complex molecules.

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

538334-18-8: The chemical substance known as (2R)-2-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid, with the CAS number 538334-18-8, is a synthetic amino acid derivative. It features a complex structure that includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect amino groups during the formation of peptide bonds. This compound exhibits characteristics typical of amino acids, such as the presence of both an amine and a carboxylic acid functional group, allowing it to participate in various chemical reactions, including peptide bond formation. The stereochemistry indicated by the (2R) and (2S) designations suggests specific spatial arrangements of the atoms, which can influence the compound's biological activity and interactions. Additionally, the presence of the fluorenyl group may enhance the compound's stability and solubility in organic solvents. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis, where it may serve as an intermediate or building block for more complex molecules.

<p>(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-alanyl-D-alanine</p>

CAS 538334-18-8

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

(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-alanyl-D-alanine

Ref: 54-OR1031964

(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-alanyl-D-alanine

Ref: 10-F634992