(4-(3-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)propoxy)-3-chlorophenyl)boronic acid

98%

  • Product Code: 89241
  CAS:    1704082-47-2
Molecular Weight: 552 g./mol Molecular Formula: C₃₀H₃₉BClNO₄Si
EC Number: MDL Number: MFCD28805771
Melting Point: Boiling Point:
Density: Storage Condition:  2-8°C
Product Description: This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds, which is essential in the construction of complex organic molecules. Its structure, featuring a piperidine ring and a tert-butyldiphenylsilyl group, enhances its stability and reactivity in various catalytic processes. This makes it valuable in the pharmaceutical industry for the synthesis of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, its application extends to materials science, where it aids in the development of advanced polymers and functional materials.
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Size (g) Availability Price Quantity
1.000 10-20 days £1,352.72
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(4-(3-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)propoxy)-3-chlorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds, which is essential in the construction of complex organic molecules. Its structure, featuring a piperidine ring and a tert-butyldiphenylsilyl group, enhances its stability and reactivity in various catalytic processes. This makes it valuable in the pharmaceutical industry for the synthesis of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, its application extends to materials science, where it aids in the development of advanced polymers and functional materials.
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