2-(N,N-Dimethylsulphamoyl)benzeneboronic Acid

≥97%

Reagent Code: #89689
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CAS Number 178432-25-2

science Other reagents with same CAS 178432-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.06 g/mol
Formula C₈H₁₂NO₄SB
badge Registry Numbers
MDL Number MFCD04039023
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in drug discovery and development. Additionally, it is utilized in the preparation of intermediates for bioactive compounds, contributing to the synthesis of potential therapeutic agents. Its stability and reactivity also make it suitable for use in research and industrial applications where precise molecular assembly is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿7,720.00
1g
10-20 days ฿14,090.00
2-(N,N-Dimethylsulphamoyl)benzeneboronic Acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in drug discovery and development. Additionally, it is utilized in the preparation

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates the coupling with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in drug discovery and development. Additionally, it is utilized in the preparation of intermediates for bioactive compounds, contributing to the synthesis of potential therapeutic agents. Its stability and reactivity also make it suitable for use in research and industrial applications where precise molecular assembly is required.

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