Methyl (S)-3-(((benzyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)propanoate

95%

Reagent Code: #233505
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CAS Number 61040-22-0

science Other reagents with same CAS 61040-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.38 g/mol
Formula C₁₇H₂₄N₂O₆
badge Registry Numbers
MDL Number MFCD22418867
thermostat Physical Properties
Melting Point 38-43 °C
Boiling Point 514.3±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.177±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of complex peptides and peptidomimetics. Its protected amino and carboxyl functional groups allow for selective deprotection and coupling in solid-phase or solution-phase peptide synthesis. Commonly employed in the preparation of biologically active molecules, including pharmaceutical intermediates and enzyme inhibitors. The stereochemistry at the alpha carbon ensures high enantioselectivity in final products, making it valuable in asymmetric synthesis. Also utilized in the development of protease substrates and diagnostic reagents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,990.00
inventory 250mg
10-20 days ฿6,760.00
inventory 1g
10-20 days ฿18,280.00
Methyl (S)-3-(((benzyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)propanoate
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Used as a chiral building block in the synthesis of complex peptides and peptidomimetics. Its protected amino and carboxyl functional groups allow for selective deprotection and coupling in solid-phase or solution-phase peptide synthesis. Commonly employed in the preparation of biologically active molecules, including pharmaceutical intermediates and enzyme inhibitors. The stereochemistry at the alpha carbon ensures high enantioselectivity in final products, making it valuable in asymmetric synthesis. Al

Used as a chiral building block in the synthesis of complex peptides and peptidomimetics. Its protected amino and carboxyl functional groups allow for selective deprotection and coupling in solid-phase or solution-phase peptide synthesis. Commonly employed in the preparation of biologically active molecules, including pharmaceutical intermediates and enzyme inhibitors. The stereochemistry at the alpha carbon ensures high enantioselectivity in final products, making it valuable in asymmetric synthesis. Also utilized in the development of protease substrates and diagnostic reagents.

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