(3-((4-Hydroxypiperidin-1-yl)sulfonyl)-4-methoxyphenyl)boronic acid

98%

  • Product Code: 65442
  CAS:    1704081-13-9
Molecular Weight: 315.16 g./mol Molecular Formula: C₁₂H₁₈BNO₆S
EC Number: MDL Number: MFCD28400425
Melting Point: Boiling Point:
Density: Storage Condition:  2-8°C
Product Description: This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is pivotal in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, particularly in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The hydroxypiperidine moiety enhances the compound's solubility and stability, making it suitable for use in aqueous or polar solvent systems. Additionally, its sulfonyl group can act as a linker or a functional handle for further chemical modifications, broadening its applicability in drug discovery and development. This chemical is also explored in the design of enzyme inhibitors and receptor ligands, leveraging its structural features to interact with biological targets effectively.
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Size (g) Availability Price Quantity
1.000 10-20 days $1,711.41
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(3-((4-Hydroxypiperidin-1-yl)sulfonyl)-4-methoxyphenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is pivotal in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, particularly in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The hydroxypiperidine moiety enhances the compound's solubility and stability, making it suitable for use in aqueous or polar solvent systems. Additionally, its sulfonyl group can act as a linker or a functional handle for further chemical modifications, broadening its applicability in drug discovery and development. This chemical is also explored in the design of enzyme inhibitors and receptor ligands, leveraging its structural features to interact with biological targets effectively.
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