2-((Tetrahydro-2H-pyran-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

97%

Reagent Code: #80679
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CAS Number 1292317-54-4

science Other reagents with same CAS 1292317-54-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.2 g/mol
Formula C₁₈H₂₄BNO₄
badge Registry Numbers
MDL Number MFCD22393670
thermostat Physical Properties
Boiling Point 477.7±45.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry, protected from light

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tetrahydro-2H-pyran-4-yloxy group enhances its solubility and stability, facilitating its use in various reaction conditions. Its application extends to the development of bioactive compounds and intermediates in drug discovery.

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Test Parameter Specification
APPEARANCE 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 100mg
10-20 days ฿5,841.00
inventory 250mg
10-20 days ฿8,640.00

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2-((Tetrahydro-2H-pyran-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tetrahydro-2H-pyran-4-yloxy group enhances it

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group serves as a key functional moiety, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tetrahydro-2H-pyran-4-yloxy group enhances its solubility and stability, facilitating its use in various reaction conditions. Its application extends to the development of bioactive compounds and intermediates in drug discovery.

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