N-(2,4-Dimethoxybenzyl)-5-Fluoro-N-(6-Fluoropyridin-2-Yl)-2-Oxo-2,3-Dihydrobenzo[D]Oxazole-6-Sulfonamide

97%

Reagent Code: #220120
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CAS Number 1607485-79-9

science Other reagents with same CAS 1607485-79-9

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Weight 477.44 g/mol
Formula C₂₁H₁₇F₂N₃O₆S
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Used as a key intermediate in the synthesis of sulfonylurea herbicides, this compound plays a critical role in agricultural chemistry for developing selective weed control agents. Its structure enables high binding affinity to plant acetolactate synthase (ALS), an enzyme essential for branched-chain amino acid synthesis. By inhibiting ALS, it effectively stops weed growth, particularly in cereal crops and turf management. The presence of fluorine atoms and methoxy groups enhances its stability, bioavailability, and selectivity, making it suitable for low-dose applications. It is also explored in research for developing new agrochemicals with improved environmental profiles and resistance management.

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inventory 100mg
10-20 days ฿45,000.00

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N-(2,4-Dimethoxybenzyl)-5-Fluoro-N-(6-Fluoropyridin-2-Yl)-2-Oxo-2,3-Dihydrobenzo[D]Oxazole-6-Sulfonamide
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Used as a key intermediate in the synthesis of sulfonylurea herbicides, this compound plays a critical role in agricultural chemistry for developing selective weed control agents. Its structure enables high binding affinity to plant acetolactate synthase (ALS), an enzyme essential for branched-chain amino acid synthesis. By inhibiting ALS, it effectively stops weed growth, particularly in cereal crops and turf management. The presence of fluorine atoms and methoxy groups enhances its stability, bioavaila

Used as a key intermediate in the synthesis of sulfonylurea herbicides, this compound plays a critical role in agricultural chemistry for developing selective weed control agents. Its structure enables high binding affinity to plant acetolactate synthase (ALS), an enzyme essential for branched-chain amino acid synthesis. By inhibiting ALS, it effectively stops weed growth, particularly in cereal crops and turf management. The presence of fluorine atoms and methoxy groups enhances its stability, bioavailability, and selectivity, making it suitable for low-dose applications. It is also explored in research for developing new agrochemicals with improved environmental profiles and resistance management.

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