Methyl 5-chloro-3-(N-(2-methoxy-2-oxoethyl)sulfamoyl)thiophene-2-carboxylate

95%

Reagent Code: #209544
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CAS Number 906522-87-0

science Other reagents with same CAS 906522-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.76 g/mol
Formula C₉H₁₀ClNO₆S₂
badge Registry Numbers
MDL Number MFCD09455046
thermostat Physical Properties
Boiling Point 480.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage Sealed and dry, 2-8℃

description Product Description

Used as an intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of certain rice field herbicides. Its structure allows for the introduction of sulfamoyl and ester functionalities, which are key in enhancing herbicidal activity and selectivity. Commonly employed in agrochemical research and development to create compounds that inhibit acetolactate synthase (ALS), an enzyme critical in branched-chain amino acid synthesis in plants. This inhibition leads to cessation of plant growth, making it effective against a broad spectrum of weeds. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies in crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,240.00
inventory 5g
10-20 days ฿30,010.00

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Methyl 5-chloro-3-(N-(2-methoxy-2-oxoethyl)sulfamoyl)thiophene-2-carboxylate
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Used as an intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of certain rice field herbicides. Its structure allows for the introduction of sulfamoyl and ester functionalities, which are key in enhancing herbicidal activity and selectivity. Commonly employed in agrochemical research and development to create compounds that inhibit acetolactate synthase (ALS), an enzyme critical in branched-chain amino acid synthesis in plants. This inhibition leads to cessation of p

Used as an intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of certain rice field herbicides. Its structure allows for the introduction of sulfamoyl and ester functionalities, which are key in enhancing herbicidal activity and selectivity. Commonly employed in agrochemical research and development to create compounds that inhibit acetolactate synthase (ALS), an enzyme critical in branched-chain amino acid synthesis in plants. This inhibition leads to cessation of plant growth, making it effective against a broad spectrum of weeds. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies in crop protection chemistry.

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