(R)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid

97%

Reagent Code: #230203
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CAS Number 132605-96-0

science Other reagents with same CAS 132605-96-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.32 g/mol
Formula C₁₂H₂₃NO₄
badge Registry Numbers
MDL Number MFCD07372887
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylic acid functionalities allow for selective peptide coupling and sequential elongation in solid-phase or solution-phase peptide synthesis. The branched aliphatic side chain enhances lipophilicity and influences conformational stability, making it valuable in optimizing drug candidates for improved metabolic stability and target binding. Commonly employed in the preparation of intermediates for antiviral and anticancer agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,410.00
inventory 250mg
10-20 days ฿27,700.00
inventory 1g
10-20 days ฿74,480.00
(R)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylic acid functionalities allow for selective peptide coupling and sequential elongation in solid-phase or solution-phase peptide synthesis. The branched aliphatic side chain enhances lipophilicity and influences conformational stability, making it valuable in optimizing drug candidates for improved metabolic stability and

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and carboxylic acid functionalities allow for selective peptide coupling and sequential elongation in solid-phase or solution-phase peptide synthesis. The branched aliphatic side chain enhances lipophilicity and influences conformational stability, making it valuable in optimizing drug candidates for improved metabolic stability and target binding. Commonly employed in the preparation of intermediates for antiviral and anticancer agents.

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