CAS 204316-31-4

Fmoc-(3S,4S)-4-Amino-3-Hydroxy-Pentanoic Acid Dcha

Description:

Fmoc-(3S,4S)-4-Amino-3-Hydroxy-Pentanoic Acid Dcha is a synthetic amino acid derivative characterized by its unique structural features that include a fluorene-9-methoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis to protect the amino group. This compound contains a chiral center, indicated by the (3S,4S) configuration, which contributes to its stereochemical properties and potential biological activity. The presence of both an amino group and a hydroxyl group on the pentanoic acid backbone enhances its reactivity and solubility in polar solvents, making it suitable for various applications in organic synthesis and medicinal chemistry. Additionally, the Dcha (dichloroacetyl) moiety may influence its pharmacokinetic properties and interactions with biological targets. Overall, this compound is of interest in the development of peptide-based therapeutics and can serve as a building block in the synthesis of more complex molecules. Its specific characteristics, such as solubility, stability, and reactivity, are essential for its application in research and development.

L-threo-Pentonic acid, 2,4,5-trideoxy-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, compd. with N-cyclohexylcyclohexanamine (1:1) (9CI)

CAS: 204316-31-4

Formula: C₂₀H₂₁NO₅

Molecular weight: 355.3844

Ref: IN-DA0029EH