2-(1-Boc-3,5-dimethyl-4-pyrazolyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #89485
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CAS Number 1073354-70-7

science Other reagents with same CAS 1073354-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.21 g/mol
Formula C₁₆H₂₇BN₂O₄
badge Registry Numbers
MDL Number MFCD09027070
thermostat Physical Properties
Melting Point 112°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable boronic ester reagent, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. Its Boc-protected pyrazole moiety enhances stability and selectivity during reactions, making it suitable for use in pharmaceutical research and the development of biologically active compounds. Additionally, it is employed in the synthesis of advanced materials and agrochemicals, where precise molecular assembly is critical. Its compatibility with various functional groups and reaction conditions makes it a versatile tool in modern synthetic chemistry.

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inventory 200mg
10-20 days ฿2,484.00

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2-(1-Boc-3,5-dimethyl-4-pyrazolyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable boronic ester reagent, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. Its Boc-protected pyrazole moiety enhances stability and selectivity during reactions, making it suitable for use in pharmaceutical research and the development of biologically active compounds. Additionally, it is employed in the

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable boronic ester reagent, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. Its Boc-protected pyrazole moiety enhances stability and selectivity during reactions, making it suitable for use in pharmaceutical research and the development of biologically active compounds. Additionally, it is employed in the synthesis of advanced materials and agrochemicals, where precise molecular assembly is critical. Its compatibility with various functional groups and reaction conditions makes it a versatile tool in modern synthetic chemistry.

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