N-(2,4-Dimethoxybenzyl)-2,5-difluoro-4-(hydroxymethyl)-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide

97%

Reagent Code: #220564
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CAS Number 2250051-37-5

science Other reagents with same CAS 2250051-37-5

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scatter_plot Molecular Information
Weight 457.47 g/mol
Formula C₁₈H₁₇F₂N₃O₅S₂
badge Registry Numbers
MDL Number MFCD32640860
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of sulfonylurea herbicides, this compound plays an important role in agricultural chemistry due to its ability to selectively inhibit acetolactate synthase (ALS) in weeds. Its structural features enable effective binding to the enzyme, disrupting branched-chain amino acid production in plants. This leads to growth inhibition and eventual death of susceptible weed species. Due to its stability and reactivity, it is also employed in the development of novel sulfonamide-based bioactive molecules for crop protection. Its application extends to research settings for designing new herbicidal agents with improved environmental and safety profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿46,350.00

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N-(2,4-Dimethoxybenzyl)-2,5-difluoro-4-(hydroxymethyl)-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide
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Used as a key intermediate in the synthesis of sulfonylurea herbicides, this compound plays an important role in agricultural chemistry due to its ability to selectively inhibit acetolactate synthase (ALS) in weeds. Its structural features enable effective binding to the enzyme, disrupting branched-chain amino acid production in plants. This leads to growth inhibition and eventual death of susceptible weed species. Due to its stability and reactivity, it is also employed in the development of novel sulfo

Used as a key intermediate in the synthesis of sulfonylurea herbicides, this compound plays an important role in agricultural chemistry due to its ability to selectively inhibit acetolactate synthase (ALS) in weeds. Its structural features enable effective binding to the enzyme, disrupting branched-chain amino acid production in plants. This leads to growth inhibition and eventual death of susceptible weed species. Due to its stability and reactivity, it is also employed in the development of novel sulfonamide-based bioactive molecules for crop protection. Its application extends to research settings for designing new herbicidal agents with improved environmental and safety profiles.

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