(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpent-4-enoic acid

98%

Reagent Code: #104201
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CAS Number 215190-23-1

science Other reagents with same CAS 215190-23-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 413.47 g/mol
Formula C₂₆H₂₃NO₄
badge Registry Numbers
MDL Number MFCD01311775
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality, ensuring selective reactions during peptide chain assembly. Its structure, including the phenylpent-4-enoic acid moiety, makes it suitable for introducing specific side-chain functionalities into peptides. It is commonly employed in research and development of pharmaceuticals, bioactive peptides, and protein studies, where precise control over peptide sequence and structure is crucial.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿6,885.00
250mg
10-20 days ฿2,700.00
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpent-4-enoic acid
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This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality, ensuring selective reactions during peptide chain assembly. Its structure, including the phenylpent-4-enoic acid moiety, makes it suitable for introducing specific side-chain functionalities into peptides. It

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality, ensuring selective reactions during peptide chain assembly. Its structure, including the phenylpent-4-enoic acid moiety, makes it suitable for introducing specific side-chain functionalities into peptides. It is commonly employed in research and development of pharmaceuticals, bioactive peptides, and protein studies, where precise control over peptide sequence and structure is crucial.

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