N-(2-methoxy-5-methylphenyl)-4-methylbenzenesulfonamid

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Reagent Code: #51877
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CAS Number 116-41-6

science Other reagents with same CAS 116-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.37 g/mol
Formula C₁₅H₁₇NO₃S
badge Registry Numbers
MDL Number MFCD00684248
thermostat Physical Properties
Boiling Point 435.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.239±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring both sulfonamide and methoxy groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic effects. Additionally, it can be employed in the creation of agrochemicals, where its properties contribute to the formulation of pesticides or herbicides. The compound’s stability and reactivity also make it suitable for use in research and development, particularly in studies focusing on the modification of aromatic systems for enhanced biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,850.00
inventory 5g
10-20 days ฿17,550.00
inventory 250mg
10-20 days ฿2,925.00

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N-(2-methoxy-5-methylphenyl)-4-methylbenzenesulfonamid
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This chemical is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring both sulfonamide and methoxy groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic effects. Additionally, it can be employed in the creation of agrochemicals, where its properties contribute to the formulation of pesticides or herbicides. The compound’s stability and reactivity also make it suitable for use in research and development, particularly in studies focusing on the modification of aromatic systems for enhanced biological activity.
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