N-Fmoc-(R)-3-(methylamino)butanoic acid

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Reagent Code: #55831
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CAS Number 1460306-60-8

science Other reagents with same CAS 1460306-60-8

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Weight 339.3851 g/mol
Formula C₂₀H₂₁NO₄
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description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision and control. The compound is especially valuable in synthesizing peptides that require the incorporation of (R)-3-(methylamino)butanoic acid, a non-natural amino acid, into their structure. Such peptides are often explored in pharmaceutical research for developing therapeutic agents, including enzyme inhibitors, receptor modulators, and bioactive peptides. Additionally, its use in SPPS enables the production of peptides with specific stereochemistry, which is crucial for their biological activity and interaction with target molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,075.00

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N-Fmoc-(R)-3-(methylamino)butanoic acid
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This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision and control. The compound is especially valuable in synthesizing peptides that require the incorporation of (R)-3-(methylamino)butanoic

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision and control. The compound is especially valuable in synthesizing peptides that require the incorporation of (R)-3-(methylamino)butanoic acid, a non-natural amino acid, into their structure. Such peptides are often explored in pharmaceutical research for developing therapeutic agents, including enzyme inhibitors, receptor modulators, and bioactive peptides. Additionally, its use in SPPS enables the production of peptides with specific stereochemistry, which is crucial for their biological activity and interaction with target molecules.

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