(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)ethoxy)-3-chlorophenyl)boronic acid

98%

Reagent Code: #89232
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CAS Number 1704074-62-3

blur_circular Chemical Specifications

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Weight 537.97 g/mol
Formula C₂₉H₃₇BClNO₄Si
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MDL Number MFCD28805757
inventory_2 Storage & Handling
Storage  2-8°C

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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables it to act as a key reagent in forming carbon-carbon bonds, which is essential in constructing complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) protecting group enhances its stability and selectivity during these reactions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its piperidine moiety contributes to its potential application in medicinal chemistry, where it may be used to develop bioactive compounds targeting specific receptors or enzymes. Its chloro substituent further allows for additional functionalization, expanding its utility in diverse chemical transformations.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days €771.20
(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)ethoxy)-3-chlorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables it to act as a key reagent in forming carbon-carbon bonds, which is essential in constructing complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) protecting group enhances its stability and selectivity during these reactions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its piperidine moiety contributes to its potential application in medicinal chemistry, where it may be used to develop bioactive compounds targeting specific receptors or enzymes. Its chloro substituent further allows for additional functionalization, expanding its utility in diverse chemical transformations.
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