(3-((2-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid

95%

  • Product Code: 36618
  CAS:    1449145-16-7
Molecular Weight: 283.15162 g./mol Molecular Formula: C₁₂H₁₈BNO₄S
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Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group, enables it to form carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules. Additionally, it is employed in the development of pharmaceuticals and agrochemicals, where its sulfonyl and piperidine moieties contribute to the design of bioactive compounds. The compound’s stability and reactivity also make it suitable for use in material science, particularly in the creation of advanced polymers and functionalized materials. Its applications extend to research and development, where it serves as a building block for exploring new chemical entities and pathways.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $222.27
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1.000 10-20 days $668.23
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5.000 10-20 days $1,896.38
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(3-((2-Methylpiperidin-1-yl)sulfonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group, enables it to form carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules. Additionally, it is employed in the development of pharmaceuticals and agrochemicals, where its sulfonyl and piperidine moieties contribute to the design of bioactive compounds. The compound’s stability and reactivity also make it suitable for use in material science, particularly in the creation of advanced polymers and functionalized materials. Its applications extend to research and development, where it serves as a building block for exploring new chemical entities and pathways.
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