(4-(N,N-Diethylsulfamoyl)-3,5-dimethylphenyl)boronic acid

98%

Reagent Code: #89253
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CAS Number 1704067-22-0

science Other reagents with same CAS 1704067-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.17 g/mol
Formula C₁₂H₂₀BNO₄S
badge Registry Numbers
MDL Number MFCD28384284
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its diethylsulfamoyl and dimethylphenyl groups contribute to its stability and reactivity, enhancing its effectiveness in various catalytic processes.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿29,230.00
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(4-(N,N-Diethylsulfamoyl)-3,5-dimethylphenyl)boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its diethylsulfamoyl and dimethylphenyl gro

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its diethylsulfamoyl and dimethylphenyl groups contribute to its stability and reactivity, enhancing its effectiveness in various catalytic processes.

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