(R)-2-(((Benzyloxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid hydrate

95%

Reagent Code: #230138
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CAS Number 210471-09-3

science Other reagents with same CAS 210471-09-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.36 g/mol
Formula C₁₆H₂₃NO₇
badge Registry Numbers
MDL Number MFCD00153327
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of peptide-based pharmaceuticals, specifically as a protected L-aspartic acid derivative (Cbz-Asp(OtBu)-OH) for solid-phase peptide synthesis. The benzyloxycarbonyl (Cbz) group protects the α-amino function, while the tert-butyl (tBu) ester safeguards the side-chain carboxylic acid, enabling selective deprotection and coupling reactions to construct complex peptide sequences with high purity and minimal side reactions. Commonly employed in research settings for developing protease inhibitors, antimicrobial agents, vaccines, and other bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿137.50
1g
10-20 days ฿154.00
5g
10-20 days ฿286.00
25g
10-20 days ฿2,560.00
100g
10-20 days ฿9,980.00
(R)-2-(((Benzyloxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid hydrate
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Used as an intermediate in the synthesis of peptide-based pharmaceuticals, specifically as a protected L-aspartic acid derivative (Cbz-Asp(OtBu)-OH) for solid-phase peptide synthesis. The benzyloxycarbonyl (Cbz) group protects the α-amino function, while the tert-butyl (tBu) ester safeguards the side-chain carboxylic acid, enabling selective deprotection and coupling reactions to construct complex peptide sequences with high purity and minimal side reactions. Commonly employed in research settings for de

Used as an intermediate in the synthesis of peptide-based pharmaceuticals, specifically as a protected L-aspartic acid derivative (Cbz-Asp(OtBu)-OH) for solid-phase peptide synthesis. The benzyloxycarbonyl (Cbz) group protects the α-amino function, while the tert-butyl (tBu) ester safeguards the side-chain carboxylic acid, enabling selective deprotection and coupling reactions to construct complex peptide sequences with high purity and minimal side reactions. Commonly employed in research settings for developing protease inhibitors, antimicrobial agents, vaccines, and other bioactive molecules.

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