1-(Mesitylene-2-sulfonyl)-3-nitro-1,2,4-triazole

99%

Reagent Code: #39622
label
Alias MSNT ; 1-(Mesityl-2-sulfone)-3-nitro-1,2,4-triazole
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CAS Number 74257-00-4

science Other reagents with same CAS 74257-00-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.31 g/mol
Formula C₁₁H₁₂N₄O₄S
badge Registry Numbers
MDL Number MFCD00009754
thermostat Physical Properties
Melting Point 134-139 °C(lit.)
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is primarily utilized in organic synthesis as a reagent for the protection of amines. Its mesitylene sulfonyl group acts as a protective moiety, shielding amines during complex chemical reactions, particularly in peptide synthesis. The nitro group enhances its reactivity, making it effective in selective transformations. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where precise control over amine reactivity is crucial. Its stability and specificity make it a valuable tool in constructing complex molecular architectures.

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Test Parameter Specification
Purity (GC) 99-100%
Appearance White to yellow solid
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿440.00
inventory 5g
10-20 days ฿1,980.00
inventory 25g
10-20 days ฿8,700.00

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1-(Mesitylene-2-sulfonyl)-3-nitro-1,2,4-triazole
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This chemical is primarily utilized in organic synthesis as a reagent for the protection of amines. Its mesitylene sulfonyl group acts as a protective moiety, shielding amines during complex chemical reactions, particularly in peptide synthesis. The nitro group enhances its reactivity, making it effective in selective transformations. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where precise control over amine reactivity is crucial. Its stability and specif

This chemical is primarily utilized in organic synthesis as a reagent for the protection of amines. Its mesitylene sulfonyl group acts as a protective moiety, shielding amines during complex chemical reactions, particularly in peptide synthesis. The nitro group enhances its reactivity, making it effective in selective transformations. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where precise control over amine reactivity is crucial. Its stability and specificity make it a valuable tool in constructing complex molecular architectures.

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