(4-(N-(3-Chloro-2-methylphenyl)sulfamoyl)phenyl)boronic acid

98%

Reagent Code: #215679
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CAS Number 957066-10-3

science Other reagents with same CAS 957066-10-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.58 g/mol
Formula C₁₃H₁₃BClNO₄S
badge Registry Numbers
MDL Number MFCD09878330
thermostat Physical Properties
Melting Point 189-191°C
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that inhibit acetolactate synthase (ALS) in plants, leading to suppression of branched-chain amino acid synthesis. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the development of complex organic molecules for crop protection agents. Also employed in medicinal chemistry research for constructing biaryl structures via palladium-catalyzed coupling reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,330.00
inventory 5g
10-20 days ฿6,980.00

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(4-(N-(3-Chloro-2-methylphenyl)sulfamoyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that inhibit acetolactate synthase (ALS) in plants, leading to suppression of branched-chain amino acid synthesis. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the development of complex organic molecules for crop protection agents. Also employed in medicinal chemistry research for constructing biaryl structures v

Used as a key intermediate in the synthesis of sulfonylurea herbicides, particularly in the production of agrochemicals that inhibit acetolactate synthase (ALS) in plants, leading to suppression of branched-chain amino acid synthesis. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the development of complex organic molecules for crop protection agents. Also employed in medicinal chemistry research for constructing biaryl structures via palladium-catalyzed coupling reactions.

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