(R)-Tert-Butyl 2-(2-(Benzyloxycarbonylamino)-2-Phenylacetamido)Acetate

98%

Reagent Code: #231568
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CAS Number 439088-73-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.45 g/mol
Formula C₂₂H₂₆N₂O₅
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of complex peptides and β-lactam antibiotics. Its protected amine and carboxylic acid groups allow selective deprotection and coupling in multi-step organic syntheses. Commonly employed in the preparation of enzyme inhibitors and pharmaceutical intermediates where stereochemistry is critical. The benzyl and tert-butyl protecting groups offer orthogonal stability under different reaction conditions, making it valuable in solid-phase and solution-phase peptide synthesis. Also utilized in the development of protease inhibitors and other bioactive molecules requiring high enantiomeric purity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,400.00
(R)-Tert-Butyl 2-(2-(Benzyloxycarbonylamino)-2-Phenylacetamido)Acetate
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Used as a chiral building block in the synthesis of complex peptides and β-lactam antibiotics. Its protected amine and carboxylic acid groups allow selective deprotection and coupling in multi-step organic syntheses. Commonly employed in the preparation of enzyme inhibitors and pharmaceutical intermediates where stereochemistry is critical. The benzyl and tert-butyl protecting groups offer orthogonal stability under different reaction conditions, making it valuable in solid-phase and solution-phase pepti

Used as a chiral building block in the synthesis of complex peptides and β-lactam antibiotics. Its protected amine and carboxylic acid groups allow selective deprotection and coupling in multi-step organic syntheses. Commonly employed in the preparation of enzyme inhibitors and pharmaceutical intermediates where stereochemistry is critical. The benzyl and tert-butyl protecting groups offer orthogonal stability under different reaction conditions, making it valuable in solid-phase and solution-phase peptide synthesis. Also utilized in the development of protease inhibitors and other bioactive molecules requiring high enantiomeric purity.

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