N-Methyl-N-isopropylsulfamoyl amide

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Reagent Code: #218839
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CAS Number 372136-76-0

science Other reagents with same CAS 372136-76-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.22 g/mol
Formula C₄H₁₂N₂O₂S
badge Registry Numbers
MDL Number MFCD11205205
thermostat Physical Properties
Boiling Point 238.7±23.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used primarily as an intermediate in the synthesis of sulfonylurea herbicides, this compound plays a key role in agricultural chemistry. It contributes to the development of crop protection agents that inhibit plant growth in weeds by targeting acetolactate synthase (ALS) enzymes. Due to its reactivity and functional structure, it is valued in forming sulfonamide linkages in agrochemical manufacturing. Its derivatives are found in selective herbicides used in rice, wheat, and other cereal crops. The compound is handled under controlled conditions due to its sensitivity and potential decomposition under heat or acidic/basic environments.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,200.00
inventory 250mg
10-20 days ฿1,880.00
inventory 1g
10-20 days ฿6,130.00
inventory 5g
10-20 days ฿26,950.00

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N-Methyl-N-isopropylsulfamoyl amide
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Used primarily as an intermediate in the synthesis of sulfonylurea herbicides, this compound plays a key role in agricultural chemistry. It contributes to the development of crop protection agents that inhibit plant growth in weeds by targeting acetolactate synthase (ALS) enzymes. Due to its reactivity and functional structure, it is valued in forming sulfonamide linkages in agrochemical manufacturing. Its derivatives are found in selective herbicides used in rice, wheat, and other cereal crops. The comp

Used primarily as an intermediate in the synthesis of sulfonylurea herbicides, this compound plays a key role in agricultural chemistry. It contributes to the development of crop protection agents that inhibit plant growth in weeds by targeting acetolactate synthase (ALS) enzymes. Due to its reactivity and functional structure, it is valued in forming sulfonamide linkages in agrochemical manufacturing. Its derivatives are found in selective herbicides used in rice, wheat, and other cereal crops. The compound is handled under controlled conditions due to its sensitivity and potential decomposition under heat or acidic/basic environments.

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