N-(tert-Butyl)-2-nitrobenzenesulfonamide

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Reagent Code: #124818
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CAS Number 363587-67-1

science Other reagents with same CAS 363587-67-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.29 g/mol
Formula C₁₀H₁₄N₂O₄S
badge Registry Numbers
MDL Number MFCD00450577
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

N-(tert-Butyl)-2-nitrobenzenesulfonamide is primarily used in organic synthesis as a protecting group for amines. Its application is significant in the preparation of complex molecules, particularly in peptide synthesis, where it helps to temporarily shield amine groups during reactions to prevent unwanted side reactions. The compound is also employed in the development of pharmaceuticals, allowing for selective modification of molecular structures. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes. Additionally, it finds use in the synthesis of agrochemicals and other fine chemicals, where precise control over functional groups is essential.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,304.00
inventory 5g
10-20 days ฿6,903.00
inventory 25g
10-20 days ฿17,253.00

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N-(tert-Butyl)-2-nitrobenzenesulfonamide
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N-(tert-Butyl)-2-nitrobenzenesulfonamide is primarily used in organic synthesis as a protecting group for amines. Its application is significant in the preparation of complex molecules, particularly in peptide synthesis, where it helps to temporarily shield amine groups during reactions to prevent unwanted side reactions. The compound is also employed in the development of pharmaceuticals, allowing for selective modification of molecular structures. Its stability under various reaction conditions makes i

N-(tert-Butyl)-2-nitrobenzenesulfonamide is primarily used in organic synthesis as a protecting group for amines. Its application is significant in the preparation of complex molecules, particularly in peptide synthesis, where it helps to temporarily shield amine groups during reactions to prevent unwanted side reactions. The compound is also employed in the development of pharmaceuticals, allowing for selective modification of molecular structures. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes. Additionally, it finds use in the synthesis of agrochemicals and other fine chemicals, where precise control over functional groups is essential.

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