2-(1H-Pyrazol-1-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

95%

Reagent Code: #91468
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CAS Number 1186115-51-4

science Other reagents with same CAS 1186115-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.13 g/mol
Formula C₁₄H₁₈BN₃O₂
badge Registry Numbers
MDL Number MFCD09607672
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, it is employed in the development of advanced materials, including organic semiconductors and polymers, due to its ability to introduce functional groups into molecular frameworks. Its pyridine and pyrazole moieties also make it a valuable ligand in coordination chemistry, aiding in the design of catalysts and metal-organic frameworks.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿11,880.00
inventory 25mg
10-20 days ฿35,680.00
inventory 100mg
10-20 days ฿120,000.00

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2-(1H-Pyrazol-1-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, it is employed in the development of advanced materials, including organic semiconductors and polymer

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, it is employed in the development of advanced materials, including organic semiconductors and polymers, due to its ability to introduce functional groups into molecular frameworks. Its pyridine and pyrazole moieties also make it a valuable ligand in coordination chemistry, aiding in the design of catalysts and metal-organic frameworks.

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