N-(Allyloxycarbonyloxy)succinimide

≥95%

Reagent Code: #84540
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CAS Number 135544-68-2

science Other reagents with same CAS 135544-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.16 g/mol
Formula C₈H₉NO₅
badge Registry Numbers
MDL Number MFCD02684388
thermostat Physical Properties
Boiling Point 269.471ºC
inventory_2 Storage & Handling
Density 1.344g/cm3
Storage room temperature, dry

description Product Description

This chemical is primarily used in organic synthesis as a protective agent for amines. It is particularly effective in peptide synthesis, where it helps to temporarily shield amine groups during reactions, preventing unwanted side reactions. The allyloxycarbonyl group it introduces can be easily removed under mild conditions, making it a versatile tool in complex molecule construction. Additionally, it finds application in the modification of biomolecules, aiding in the study of protein interactions and functions. Its stability and selective reactivity make it valuable in pharmaceutical research and development, particularly in the design of drug candidates and bioactive compounds.

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Test Parameter Specification
Appearance Colorless to pale yellow liquid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿945.00

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N-(Allyloxycarbonyloxy)succinimide
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This chemical is primarily used in organic synthesis as a protective agent for amines. It is particularly effective in peptide synthesis, where it helps to temporarily shield amine groups during reactions, preventing unwanted side reactions. The allyloxycarbonyl group it introduces can be easily removed under mild conditions, making it a versatile tool in complex molecule construction. Additionally, it finds application in the modification of biomolecules, aiding in the study of protein interactions and

This chemical is primarily used in organic synthesis as a protective agent for amines. It is particularly effective in peptide synthesis, where it helps to temporarily shield amine groups during reactions, preventing unwanted side reactions. The allyloxycarbonyl group it introduces can be easily removed under mild conditions, making it a versatile tool in complex molecule construction. Additionally, it finds application in the modification of biomolecules, aiding in the study of protein interactions and functions. Its stability and selective reactivity make it valuable in pharmaceutical research and development, particularly in the design of drug candidates and bioactive compounds.

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