N-Carbobenzoxy-2-nitrobenzenesulfonamide

≥98%

Reagent Code: #78351
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CAS Number 245365-64-4

science Other reagents with same CAS 245365-64-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.32 g/mol
Formula C₁₄H₁₂N₂O₆S
badge Registry Numbers
MDL Number MFCD06797080
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used primarily in organic synthesis as a protecting group for amines, particularly in peptide synthesis. It helps prevent unwanted reactions at the amine site during complex chemical processes. Its nitrobenzenesulfonamide component provides stability under various reaction conditions, making it suitable for multi-step synthetic routes. Additionally, it can be selectively removed under mild conditions, allowing for the controlled deprotection of amines without disrupting other functional groups in the molecule. This makes it a valuable tool in the development of pharmaceuticals and biologically active compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,314.00
inventory 5g
10-20 days ฿3,213.00

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N-Carbobenzoxy-2-nitrobenzenesulfonamide
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Used primarily in organic synthesis as a protecting group for amines, particularly in peptide synthesis. It helps prevent unwanted reactions at the amine site during complex chemical processes. Its nitrobenzenesulfonamide component provides stability under various reaction conditions, making it suitable for multi-step synthetic routes. Additionally, it can be selectively removed under mild conditions, allowing for the controlled deprotection of amines without disrupting other functional groups in the mol

Used primarily in organic synthesis as a protecting group for amines, particularly in peptide synthesis. It helps prevent unwanted reactions at the amine site during complex chemical processes. Its nitrobenzenesulfonamide component provides stability under various reaction conditions, making it suitable for multi-step synthetic routes. Additionally, it can be selectively removed under mild conditions, allowing for the controlled deprotection of amines without disrupting other functional groups in the molecule. This makes it a valuable tool in the development of pharmaceuticals and biologically active compounds.

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