N-(tert-Butoxycarbonyl)-2-nitrobenzenesulfonamide

≥98%

Reagent Code: #78350
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CAS Number 198572-71-3

science Other reagents with same CAS 198572-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.3 g/mol
Formula C₁₁H₁₄N₂O₆S
badge Registry Numbers
MDL Number MFCD06796217
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used in organic synthesis as a protecting group for amines. Its application is particularly valuable in peptide synthesis, where it helps to selectively protect amino groups during the formation of peptide bonds. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, allowing for precise control over the synthesis process. Additionally, the nitrobenzenesulfonamide moiety can be selectively removed under mild conditions, making it a versatile tool in multi-step synthetic routes. This compound is also utilized in the preparation of complex molecules in medicinal chemistry, where protecting groups are essential to achieve desired chemical transformations without unwanted side reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,241.00
inventory 200mg
10-20 days ฿891.00

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N-(tert-Butoxycarbonyl)-2-nitrobenzenesulfonamide
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This chemical is primarily used in organic synthesis as a protecting group for amines. Its application is particularly valuable in peptide synthesis, where it helps to selectively protect amino groups during the formation of peptide bonds. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, allowing for precise control over the synthesis process. Additionally, the nitrobenzenesulfonamide moiety can be selectively removed under mild conditions, making it a versatile t

This chemical is primarily used in organic synthesis as a protecting group for amines. Its application is particularly valuable in peptide synthesis, where it helps to selectively protect amino groups during the formation of peptide bonds. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, allowing for precise control over the synthesis process. Additionally, the nitrobenzenesulfonamide moiety can be selectively removed under mild conditions, making it a versatile tool in multi-step synthetic routes. This compound is also utilized in the preparation of complex molecules in medicinal chemistry, where protecting groups are essential to achieve desired chemical transformations without unwanted side reactions.

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