P-Toluenesulfonyl Azide

≥99%(75% in ethyl acetate solution)

Reagent Code: #224926
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CAS Number 941-55-9

science Other reagents with same CAS 941-55-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.22 g/mol
Formula C₇H₇N₃O₂S
badge Registry Numbers
MDL Number MFCD00180767
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used in organic synthesis, particularly as a reagent for introducing azide groups into organic molecules. It serves as a safe and convenient source of nitrene equivalents in metal-catalyzed aziridination reactions, enabling the formation of aziridine rings from alkenes. Commonly employed in the synthesis of nitrogen-containing heterocycles and amines through reduction of the azide group. Also utilized in the preparation of sulfonamides and in click chemistry applications where azide-alkyne cycloadditions are required. Its stability and ease of handling make it preferable over more explosive azide reagents in laboratory settings.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿300.00
25g
10-20 days ฿520.00
100g
10-20 days ฿1,340.00
500g
10-20 days ฿4,180.00
2.5kg
10-20 days ฿15,660.00
P-Toluenesulfonyl Azide
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Widely used in organic synthesis, particularly as a reagent for introducing azide groups into organic molecules. It serves as a safe and convenient source of nitrene equivalents in metal-catalyzed aziridination reactions, enabling the formation of aziridine rings from alkenes. Commonly employed in the synthesis of nitrogen-containing heterocycles and amines through reduction of the azide group. Also utilized in the preparation of sulfonamides and in click chemistry applications where azide-alkyne cycload

Widely used in organic synthesis, particularly as a reagent for introducing azide groups into organic molecules. It serves as a safe and convenient source of nitrene equivalents in metal-catalyzed aziridination reactions, enabling the formation of aziridine rings from alkenes. Commonly employed in the synthesis of nitrogen-containing heterocycles and amines through reduction of the azide group. Also utilized in the preparation of sulfonamides and in click chemistry applications where azide-alkyne cycloadditions are required. Its stability and ease of handling make it preferable over more explosive azide reagents in laboratory settings.

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