N-Methyl-N-nitrosotoluene-4-sulphonamide

98%

Reagent Code: #216965
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CAS Number 80-11-5

science Other reagents with same CAS 80-11-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.24 g/mol
Formula C₈H₁₀N₂O₃S
badge Registry Numbers
MDL Number MFCD00002050
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used primarily as a chemical reagent in organic synthesis, this compound serves as a source of diazomethane when treated with base. Diazomethane is widely used for methylating carboxylic acids, phenols, and other acidic functional groups due to its high reactivity and selectivity. It is also employed in the preparation of heterocyclic compounds and in cyclopropanation reactions. Because of its ability to generate diazomethane in situ, it is favored in laboratories where safe, controlled release of diazomethane is required. Its solid form makes it easier and safer to handle compared to gaseous diazomethane. Commonly used in pharmaceutical and agrochemical research for introducing methyl groups under mild conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿330.00
25g
10-20 days ฿500.00
100g
10-20 days ฿1,650.00
500g
10-20 days ฿6,620.00
N-Methyl-N-nitrosotoluene-4-sulphonamide
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Used primarily as a chemical reagent in organic synthesis, this compound serves as a source of diazomethane when treated with base. Diazomethane is widely used for methylating carboxylic acids, phenols, and other acidic functional groups due to its high reactivity and selectivity. It is also employed in the preparation of heterocyclic compounds and in cyclopropanation reactions. Because of its ability to generate diazomethane in situ, it is favored in laboratories where safe, controlled release of diazometh
Used primarily as a chemical reagent in organic synthesis, this compound serves as a source of diazomethane when treated with base. Diazomethane is widely used for methylating carboxylic acids, phenols, and other acidic functional groups due to its high reactivity and selectivity. It is also employed in the preparation of heterocyclic compounds and in cyclopropanation reactions. Because of its ability to generate diazomethane in situ, it is favored in laboratories where safe, controlled release of diazomethane is required. Its solid form makes it easier and safer to handle compared to gaseous diazomethane. Commonly used in pharmaceutical and agrochemical research for introducing methyl groups under mild conditions.
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