1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

97%

Reagent Code: #89491
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CAS Number 1003846-21-6

science Other reagents with same CAS 1003846-21-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.16 g/mol
Formula C₁₄H₂₃BN₂O₃
badge Registry Numbers
MDL Number MFCD16556148
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The tetrahydro-2H-pyran (THP) protecting group enhances its stability during synthesis, allowing for selective transformations. It is often employed in the preparation of biologically active compounds, including drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, its structure is advantageous in the development of advanced materials and functionalized polymers.

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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 5g
10-20 days ฿950.00
inventory 25g
10-20 days ฿3,880.00

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1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The tetrahydro-2H-pyran (THP) protecting group enhances its stability during synthesis, allowing for selective transformations. It is often employed in the preparation of biologically active compounds, including drug candid

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical and agrochemical research. The tetrahydro-2H-pyran (THP) protecting group enhances its stability during synthesis, allowing for selective transformations. It is often employed in the preparation of biologically active compounds, including drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, its structure is advantageous in the development of advanced materials and functionalized polymers.

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