(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)carbonyl)amino)butanoic acid

95%

Reagent Code: #37651
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CAS Number 369611-58-5

science Other reagents with same CAS 369611-58-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 474.5200 g/mol
Formula C₂₇H₂₆N₂O₆
badge Registry Numbers
MDL Number MFCD06796914
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description Product Description

This compound is primarily utilized in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality, while the benzyloxycarbonyl (Z) group protects the side chain amine. This dual protection strategy allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise construction of complex peptides. Its application is critical in the production of peptides for pharmaceutical research, drug development, and biochemical studies, ensuring high purity and specificity in the final peptide product.

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inventory 100mg
10-20 days ฿2,583.00

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(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)carbonyl)amino)butanoic acid
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This compound is primarily utilized in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality, while the benzyloxycarbonyl (Z) group protects the side chain amine. This dual protection strategy allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise construction of complex peptides. Its application is critical in the production of peptides for

This compound is primarily utilized in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality, while the benzyloxycarbonyl (Z) group protects the side chain amine. This dual protection strategy allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise construction of complex peptides. Its application is critical in the production of peptides for pharmaceutical research, drug development, and biochemical studies, ensuring high purity and specificity in the final peptide product.

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