(R)-tert-Butyl3-((tert-butoxycarbonyl)amino)-4-hydroxybutanoate

98%

Reagent Code: #231983
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CAS Number 439150-76-2

science Other reagents with same CAS 439150-76-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.34 g/mol
Formula C₁₃H₂₅NO₅
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

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 hydroxyl and protected amino groups allow for selective functionalization, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of peptidomimetics and intermediates for drug candidates targeting viral infections and metabolic disorders. The tert-butyl protecting groups facilitate easy deprotection under mild acidic conditions, enabling efficient downstream processing in medicinal chemistry workflows.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿22,700.00
250mg
10-20 days ฿37,910.00
1g
10-20 days ฿75,820.00
(R)-tert-Butyl3-((tert-butoxycarbonyl)amino)-4-hydroxybutanoate
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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 hydroxyl and protected amino groups allow for selective functionalization, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of peptidomimetics and intermediates for drug candidates targeting viral infections and metabolic disorders. The tert-butyl protecting groups facilitate easy deprotection under mild acid

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its hydroxyl and protected amino groups allow for selective functionalization, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of peptidomimetics and intermediates for drug candidates targeting viral infections and metabolic disorders. The tert-butyl protecting groups facilitate easy deprotection under mild acidic conditions, enabling efficient downstream processing in medicinal chemistry workflows.

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