CAS 1217731-48-0: (Alphar)-Alpha-[[(9H-Fluoren-9-Ylmethoxy)Carbonyl]Amino]Benzenepentanoic Acid

Description: (Alphar)-Alpha-[[(9H-Fluoren-9-Ylmethoxy)Carbonyl]Amino]Benzenepentanoic Acid, identified by its CAS number 1217731-48-0, is a synthetic organic compound characterized by its complex structure, which includes a fluorenylmethoxycarbonyl (Fmoc) protecting group and a pentanoic acid moiety. This compound is typically used in peptide synthesis and bioconjugation due to its ability to protect amino groups during chemical reactions. The fluorenyl group provides stability and facilitates purification processes, while the pentanoic acid chain contributes to the hydrophobic properties of the molecule. Its solubility characteristics may vary depending on the solvent used, and it is generally soluble in organic solvents but less so in water. The compound's reactivity is influenced by the presence of the carboxylic acid functional group, which can participate in various chemical reactions, including esterification and amidation. Overall, this compound is significant in the field of medicinal chemistry and peptide research, serving as a versatile building block for more complex molecular architectures.

Benzenepentanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αR)-

CAS: 1217731-48-0

• Formula: C₂₆H₂₅NO₄
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 415.481

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpentanoic acid

CAS: 1217731-48-0

• Purity: 0.95
• Molecular weight: 415.48g/mol

(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpentanoic acid

CAS: 1217731-48-0

• Purity: 97%
• Molecular weight: 415.489013671875

Fmoc-D-2-amino-5-phenylpentanoic acid

CAS: 1217731-48-0

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• Formula: C₂₆H₂₅NO₄
• Purity: Min. 95%
• Molecular weight: 415.48 g/mol