3-Chloro-5-methanesulfonylbenzoic acid

98%

Reagent Code: #156617
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CAS Number 151104-63-1

science Other reagents with same CAS 151104-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.66 g/mol
Formula C₈H₇ClO₄S
badge Registry Numbers
MDL Number MFCD24108576
thermostat Physical Properties
Boiling Point 484.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.507±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that target broadleaf weeds in crops like rice and wheat. Its structure allows for the formation of sulfonamide bonds essential for herbicidal activity. Commonly employed in the development of environmentally persistent weed control agents due to its stability and reactivity in coupling reactions. Also utilized in the preparation of other biologically active molecules in agricultural chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,940.00
inventory 250mg
10-20 days ฿6,680.00
inventory 5g
10-20 days ฿62,870.00
inventory 1g
10-20 days ฿17,980.00

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3-Chloro-5-methanesulfonylbenzoic acid
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Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that target broadleaf weeds in crops like rice and wheat. Its structure allows for the formation of sulfonamide bonds essential for herbicidal activity. Commonly employed in the development of environmentally persistent weed control agents due to its stability and reactivity in coupling reactions. Also utilized in the preparation of other biologically active molecules in agricultural ch

Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that target broadleaf weeds in crops like rice and wheat. Its structure allows for the formation of sulfonamide bonds essential for herbicidal activity. Commonly employed in the development of environmentally persistent weed control agents due to its stability and reactivity in coupling reactions. Also utilized in the preparation of other biologically active molecules in agricultural chemistry.

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