dimethyl [(4-chlorobenzoyl)amino]malonate

Reagent Code: #168401
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CAS Number 91396-09-7

science Other reagents with same CAS 91396-09-7

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Weight 285.684 g/mol
Formula C₁₂H₁₂ClNO₅
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of agrochemicals, particularly sulfonylurea herbicides, and pharmaceuticals. It plays a key role in developing efficient, low-dose herbicides that control broadleaf weeds in crops such as corn and soybeans by enabling the formation of active ingredients that inhibit the enzyme acetolactate synthase (ALS), essential for amino acid synthesis in plants, leading to weed growth cessation and death. Also used in the development of fungicides. Its structure, featuring reactive functional groups, allows for easy modification to target specific plant enzymes or microbial processes. Commonly employed in research to design new bioactive molecules with reduced environmental impact.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,000.00

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dimethyl [(4-chlorobenzoyl)amino]malonate
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Used as an intermediate in the synthesis of agrochemicals, particularly sulfonylurea herbicides, and pharmaceuticals. It plays a key role in developing efficient, low-dose herbicides that control broadleaf weeds in crops such as corn and soybeans by enabling the formation of active ingredients that inhibit the enzyme acetolactate synthase (ALS), essential for amino acid synthesis in plants, leading to weed growth cessation and death. Also used in the development of fungicides. Its structure, featuring re

Used as an intermediate in the synthesis of agrochemicals, particularly sulfonylurea herbicides, and pharmaceuticals. It plays a key role in developing efficient, low-dose herbicides that control broadleaf weeds in crops such as corn and soybeans by enabling the formation of active ingredients that inhibit the enzyme acetolactate synthase (ALS), essential for amino acid synthesis in plants, leading to weed growth cessation and death. Also used in the development of fungicides. Its structure, featuring reactive functional groups, allows for easy modification to target specific plant enzymes or microbial processes. Commonly employed in research to design new bioactive molecules with reduced environmental impact.

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