2-(N,N-Dimethylsulphamoyl)benzeneboronic Acid
≥97%
- Product Code: 89689
CAS:
178432-25-2
Molecular Weight: | 229.06 g./mol | Molecular Formula: | C₈H₁₂NO₄SB |
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EC Number: | MDL Number: | MFCD04039023 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
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.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿7,720.00 |
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1.000 | 10-20 days | ฿14,090.00 |
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2-(N,N-Dimethylsulphamoyl)benzeneboronic Acid
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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