tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxylate

97%

Reagent Code: #118491
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CAS Number 956136-85-9

science Other reagents with same CAS 956136-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 387.32 g/mol
Formula C₂₂H₃₄BNO₄
badge Registry Numbers
MDL Number MFCD16652353
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the introduction of the phenylpiperidine moiety into more complex molecules. Its boronate ester group makes it highly reactive towards aryl halides, enabling the formation of carbon-carbon bonds. This is particularly valuable in the pharmaceutical industry for the development of drug candidates, especially those targeting the central nervous system. Additionally, it is utilized in materials science for the synthesis of organic electronic materials, where precise molecular architecture is crucial for performance.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,770.00
inventory 1g
10-20 days ฿11,934.00
inventory 100mg
10-20 days ฿2,790.00

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tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxylate
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the introduction of the phenylpiperidine moiety into more complex molecules. Its boronate ester group makes it highly reactive towards aryl halides, enabling the formation of carbon-carbon bonds. This is particularly valuable in the pharmaceutical industry for the development of drug candidates, especially those targeting the central nervo

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the introduction of the phenylpiperidine moiety into more complex molecules. Its boronate ester group makes it highly reactive towards aryl halides, enabling the formation of carbon-carbon bonds. This is particularly valuable in the pharmaceutical industry for the development of drug candidates, especially those targeting the central nervous system. Additionally, it is utilized in materials science for the synthesis of organic electronic materials, where precise molecular architecture is crucial for performance.

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