O-tert-Butyl-L-threonine tert-Butyl Ester

96.0%

Reagent Code: #221396
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CAS Number 5854-78-4

science Other reagents with same CAS 5854-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.34 g/mol
Formula C₁₂H₂₅NO₃
badge Registry Numbers
MDL Number MFCD00077109
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a chiral building block in the synthesis of complex pharmaceuticals and bioactive molecules. Its protected functional groups make it valuable in peptide synthesis, especially where stereochemical control is required. Commonly employed in the development of protease inhibitors and other therapeutic agents that demand high enantiomeric purity. The tert-butyl groups enhance lipophilicity and stability during synthetic transformations, making it suitable for solid-phase peptide synthesis and medicinal chemistry applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿240.00
5g
10-20 days ฿360.00
25g
10-20 days ฿1,560.00
100g
10-20 days ฿5,720.00
O-tert-Butyl-L-threonine tert-Butyl Ester
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Used as a chiral building block in the synthesis of complex pharmaceuticals and bioactive molecules. Its protected functional groups make it valuable in peptide synthesis, especially where stereochemical control is required. Commonly employed in the development of protease inhibitors and other therapeutic agents that demand high enantiomeric purity. The tert-butyl groups enhance lipophilicity and stability during synthetic transformations, making it suitable for solid-phase peptide synthesis and medicina

Used as a chiral building block in the synthesis of complex pharmaceuticals and bioactive molecules. Its protected functional groups make it valuable in peptide synthesis, especially where stereochemical control is required. Commonly employed in the development of protease inhibitors and other therapeutic agents that demand high enantiomeric purity. The tert-butyl groups enhance lipophilicity and stability during synthetic transformations, making it suitable for solid-phase peptide synthesis and medicinal chemistry applications.

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