Benzyl 2-(((benzyloxy)carbonyl)amino)acrylate

≥95%

Reagent Code: #41107
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CAS Number 59524-07-1

science Other reagents with same CAS 59524-07-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.33 g/mol
Formula C₁₈H₁₇NO₄
badge Registry Numbers
MDL Number MFCD28369506
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a key intermediate in the construction of complex molecules due to its reactive acrylate and protected amino groups. The benzyl and benzyloxycarbonyl (Cbz) groups act as protective moieties, ensuring selective reactivity during multi-step synthetic processes. It is commonly employed in the development of pharmaceuticals, where precise control over molecular structure is critical. Additionally, it finds use in research settings for studying reaction mechanisms and developing novel synthetic methodologies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿19,719.00
100mg
10-20 days ฿3,942.00
250mg
10-20 days ฿6,570.00
Benzyl 2-(((benzyloxy)carbonyl)amino)acrylate
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This chemical is primarily utilized in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a key intermediate in the construction of complex molecules due to its reactive acrylate and protected amino groups. The benzyl and benzyloxycarbonyl (Cbz) groups act as protective moieties, ensuring selective reactivity during multi-step synthetic processes. It is commonly employed in the development of pharmaceuticals, where precise control over mol

This chemical is primarily utilized in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a key intermediate in the construction of complex molecules due to its reactive acrylate and protected amino groups. The benzyl and benzyloxycarbonyl (Cbz) groups act as protective moieties, ensuring selective reactivity during multi-step synthetic processes. It is commonly employed in the development of pharmaceuticals, where precise control over molecular structure is critical. Additionally, it finds use in research settings for studying reaction mechanisms and developing novel synthetic methodologies.

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