CAS 200335-41-7: Fmoc-D-Asp-NH2

Description: Fmoc-D-Asp-NH2, or 9-fluorenylmethoxycarbonyl-D-aspartic acid amide, is a derivative of aspartic acid commonly used in peptide synthesis and research. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which is utilized to shield the amino group during the synthesis of peptides, allowing for selective reactions at other functional groups. The presence of the D-aspartic acid moiety indicates that it is an enantiomer of aspartic acid, which can influence the biological activity and properties of the resulting peptides. Fmoc-D-Asp-NH2 is typically a white to off-white solid and is soluble in organic solvents like dimethyl sulfoxide (DMSO) and dimethylformamide (DMF), but less soluble in water. Its stability under standard laboratory conditions makes it a valuable intermediate in the synthesis of various bioactive peptides. Additionally, the compound's structure allows for easy removal of the Fmoc group under mild basic conditions, facilitating the continuation of peptide synthesis.

Formula: C₁₉H₁₈N₂O₅

Butanoic acid, 4-amino-3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-oxo-, (3R)-

CAS: 200335-41-7

• Formula: C₁₉H₁₈N₂O₅
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 354.35662

(3R)-4-Amino-3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-oxobutanoic acid

CAS: 200335-41-7

• Purity: 95%
• Molecular weight: 354.36g/mol

FMOC-D-ASP-NH2

CAS: 200335-41-7

• Purity: 98%
• Molecular weight: 354.36199951171875

Fmoc-D-aspartic acid α-amide

CAS: 200335-41-7

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• Formula: C₁₉H₁₈N₂O₅
• Purity: Min. 95%
• Molecular weight: 354.36 g/mol