The chemical substance known as "(2R,3S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)amino)-3-hydroxybutanoic acid hydrate" is a derivative of amino acids, characterized by the presence of a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis. This compound features a chiral center at the 2nd and 3rd carbon atoms, indicating its stereochemistry as (2R,3S). The presence of a hydroxy group at the 3rd carbon contributes to its potential reactivity and solubility in polar solvents. The hydrate form suggests that the compound can associate with water molecules, which may influence its stability and solubility. This substance is likely to be utilized in biochemical applications, particularly in the synthesis of peptides or as a building block in organic synthesis due to its functional groups. Its specific stereochemistry and functional groups make it a valuable compound in medicinal chemistry and drug development, where precise molecular configurations are crucial for biological activity.

(2R,3S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-3-hydroxybutanoic acid hydrate

1272755-74-4: The chemical substance known as "(2R,3S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)amino)-3-hydroxybutanoic acid hydrate" is a derivative of amino acids, characterized by the presence of a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis. This compound features a chiral center at the 2nd and 3rd carbon atoms, indicating its stereochemistry as (2R,3S). The presence of a hydroxy group at the 3rd carbon contributes to its potential reactivity and solubility in polar solvents. The hydrate form suggests that the compound can associate with water molecules, which may influence its stability and solubility. This substance is likely to be utilized in biochemical applications, particularly in the synthesis of peptides or as a building block in organic synthesis due to its functional groups. Its specific stereochemistry and functional groups make it a valuable compound in medicinal chemistry and drug development, where precise molecular configurations are crucial for biological activity.

CAS 1272755-74-4

(2R,3S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-3-hydroxybutanoic acid hydrate

(2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid hydrate

Ref: IN-DA000WUN

(2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoic acid hydrate

Ref: 10-F328704