N-(2-Chlorobenzyloxycarbonyloxy)succinimide

98%

Reagent Code: #116539
label
Alias 2-Chloro-N-succinimidyl carbonate ; 2-Chlorobenzyl-N-succinimidyl carbonate
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CAS Number 65853-65-8

science Other reagents with same CAS 65853-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.66 g/mol
Formula C₁₂H₁₀ClNO₅
badge Registry Numbers
MDL Number MFCD00010743
thermostat Physical Properties
Melting Point 102-105 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis as a protective agent for amines. It reacts with amine groups to form stable carbamate derivatives, shielding the amines during subsequent reactions. This is particularly useful in peptide synthesis, where selective protection and deprotection of functional groups are essential. Additionally, it can be employed in the preparation of pharmaceuticals and bioactive molecules, ensuring precise control over reaction pathways. Its stability and reactivity make it a valuable tool in complex chemical transformations.

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Test Parameter Specification
Melting Point 103-105°C
Purity (Titration with Agno3) 97.5-102.5
Appearance White powder or crystals
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿4,620.00
inventory 5g
10-20 days ฿330.00
inventory 500g
10-20 days ฿18,350.00
inventory 25g
10-20 days ฿1,520.00

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N-(2-Chlorobenzyloxycarbonyloxy)succinimide
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This chemical is primarily utilized in organic synthesis as a protective agent for amines. It reacts with amine groups to form stable carbamate derivatives, shielding the amines during subsequent reactions. This is particularly useful in peptide synthesis, where selective protection and deprotection of functional groups are essential. Additionally, it can be employed in the preparation of pharmaceuticals and bioactive molecules, ensuring precise control over reaction pathways. Its stability and reactivit

This chemical is primarily utilized in organic synthesis as a protective agent for amines. It reacts with amine groups to form stable carbamate derivatives, shielding the amines during subsequent reactions. This is particularly useful in peptide synthesis, where selective protection and deprotection of functional groups are essential. Additionally, it can be employed in the preparation of pharmaceuticals and bioactive molecules, ensuring precise control over reaction pathways. Its stability and reactivity make it a valuable tool in complex chemical transformations.

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