Tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate

95%

Reagent Code: #91029
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CAS Number 1402174-61-1

science Other reagents with same CAS 1402174-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.18 g/mol
Formula C₁₅H₂₅BN₂O₄
badge Registry Numbers
MDL Number MFCD21099685
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for the preparation of complex organic molecules, especially in pharmaceutical research and development. The boronate ester group in the structure makes it a valuable reagent for constructing carbon-carbon bonds, which is essential in creating active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, its pyrazole core is often utilized in the design of compounds with potential biological activity, such as anti-inflammatory or anticancer agents. The tert-butyl protecting group enhances stability during synthetic processes, making it easier to handle and manipulate in multi-step reactions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,552.00
inventory 100mg
10-20 days ฿46,674.00

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Tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for the preparation of complex organic molecules, especially in pharmaceutical research and development. The boronate ester group in the structure makes it a valuable reagent for constructing carbon-carbon bonds, which is essential in creating active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, its pyrazole core is oft

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for the preparation of complex organic molecules, especially in pharmaceutical research and development. The boronate ester group in the structure makes it a valuable reagent for constructing carbon-carbon bonds, which is essential in creating active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, its pyrazole core is often utilized in the design of compounds with potential biological activity, such as anti-inflammatory or anticancer agents. The tert-butyl protecting group enhances stability during synthetic processes, making it easier to handle and manipulate in multi-step reactions.

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