(S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate

≥95%

Reagent Code: #37796
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CAS Number 77215-55-5

science Other reagents with same CAS 77215-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.35 g/mol
Formula C₁₅H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD09991588
thermostat Physical Properties
Boiling Point 444.3±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the tert-butyl group safeguards the carboxyl function, and the benzyloxycarbonyl (Cbz) group protects the amino function. This dual protection allows for selective deprotection during multi-step organic syntheses, particularly in the production of complex peptide structures. It is also employed in the development of bioactive molecules and drug candidates, where precise control over amino acid reactivity is essential. Additionally, its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds for use in medicinal chemistry and drug discovery.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white Solid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,901.00
inventory 100mg
10-20 days ฿765.00
inventory 1g
10-20 days ฿2,592.00
inventory 250mg
10-20 days ฿1,260.00

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(S)-tert-Butyl 3-amino-2-(((benzyloxy)carbonyl)amino)propanoate
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This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the tert-butyl group safeguards the carboxyl function, and the benzyloxycarbonyl (Cbz) group protects the amino function. This dual protection allows for selective deprotection during multi-step organic syntheses, particularly in the production of complex peptide structures. It is also employed in the development of bioactive molecules and drug candidate

This compound is primarily utilized in the synthesis of peptides and pharmaceutical intermediates. It serves as a protected amino acid derivative, where the tert-butyl group safeguards the carboxyl function, and the benzyloxycarbonyl (Cbz) group protects the amino function. This dual protection allows for selective deprotection during multi-step organic syntheses, particularly in the production of complex peptide structures. It is also employed in the development of bioactive molecules and drug candidates, where precise control over amino acid reactivity is essential. Additionally, its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds for use in medicinal chemistry and drug discovery.

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