tert-butyl ((4-(dimethyl-l4-azanylidene)pyridin-1(4H)-yl)sulfonyl)carbamate

97%(HPLC) 

Reagent Code: #52255
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CAS Number 352275-00-4

science Other reagents with same CAS 352275-00-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.36 g/mol
Formula C₁₂H₁₉N₃O₄S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis as a protecting group for amines, particularly in peptide and protein chemistry. Its role is to safeguard amine functionalities during complex reactions, ensuring selective transformations without unwanted side reactions. The tert-butyl group provides stability under various conditions, while the sulfonylcarbamate moiety allows for easy deprotection when needed. This compound is especially valuable in the synthesis of biologically active molecules, where precise control over reaction steps is critical. Its application extends to medicinal chemistry, where it aids in the development of pharmaceuticals by enabling the construction of intricate molecular structures with high precision.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 96.5-100%
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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tert-butyl ((4-(dimethyl-l4-azanylidene)pyridin-1(4H)-yl)sulfonyl)carbamate
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This chemical is primarily utilized in organic synthesis as a protecting group for amines, particularly in peptide and protein chemistry. Its role is to safeguard amine functionalities during complex reactions, ensuring selective transformations without unwanted side reactions. The tert-butyl group provides stability under various conditions, while the sulfonylcarbamate moiety allows for easy deprotection when needed. This compound is especially valuable in the synthesis of biologically active molecules, wh
This chemical is primarily utilized in organic synthesis as a protecting group for amines, particularly in peptide and protein chemistry. Its role is to safeguard amine functionalities during complex reactions, ensuring selective transformations without unwanted side reactions. The tert-butyl group provides stability under various conditions, while the sulfonylcarbamate moiety allows for easy deprotection when needed. This compound is especially valuable in the synthesis of biologically active molecules, where precise control over reaction steps is critical. Its application extends to medicinal chemistry, where it aids in the development of pharmaceuticals by enabling the construction of intricate molecular structures with high precision.
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