N-(Allyloxy)-2-Nitrobenzenesulfonamide

≥94%

Reagent Code: #217556
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CAS Number 359442-67-4

science Other reagents with same CAS 359442-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.25 g/mol
Formula C₉H₁₀N₂O₅S
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the protection and deprotection of amines during peptide and complex molecule construction. Its allyloxy group allows for selective removal under mild conditions using palladium catalysts, making it valuable in multi-step syntheses where functional group compatibility is crucial. Commonly employed in the development of pharmaceuticals and agrochemicals due to its stability under various reaction conditions and clean deprotection profile. Also utilized in the preparation of sulfonamide-based bioactive compounds, where controlled release of the amine functionality is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿670.00
1g
10-20 days ฿1,830.00
5g
10-20 days ฿6,080.00
10g
10-20 days ฿10,390.00
25g
10-20 days ฿22,500.00
N-(Allyloxy)-2-Nitrobenzenesulfonamide
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Used as a key intermediate in organic synthesis, particularly in the protection and deprotection of amines during peptide and complex molecule construction. Its allyloxy group allows for selective removal under mild conditions using palladium catalysts, making it valuable in multi-step syntheses where functional group compatibility is crucial. Commonly employed in the development of pharmaceuticals and agrochemicals due to its stability under various reaction conditions and clean deprotection profile. Also
Used as a key intermediate in organic synthesis, particularly in the protection and deprotection of amines during peptide and complex molecule construction. Its allyloxy group allows for selective removal under mild conditions using palladium catalysts, making it valuable in multi-step syntheses where functional group compatibility is crucial. Commonly employed in the development of pharmaceuticals and agrochemicals due to its stability under various reaction conditions and clean deprotection profile. Also utilized in the preparation of sulfonamide-based bioactive compounds, where controlled release of the amine functionality is required.
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