(1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid

98%

Reagent Code: #91015
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CAS Number 1188405-87-9

science Other reagents with same CAS 1188405-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.01 g/mol
Formula C₈H₁₃BN₂O₄
thermostat Physical Properties
Melting Point 157-161°C
Boiling Point 374.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the introduction of the pyrazole moiety into more complex molecules, which are often explored in pharmaceutical research. The tert-butoxycarbonyl (Boc) protecting group enhances the stability of the compound during synthetic processes, allowing for selective reactions at the boronic acid site. Its applications extend to the development of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, it is used in the preparation of ligands for catalysis and materials science research, where precise molecular architecture is crucial.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿750.00
inventory 1g
10-20 days ฿1,600.00
inventory 5g
10-20 days ฿7,150.00

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(1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the introduction of the pyrazole moiety into more complex molecules, which are often explored in pharmaceutical research. The tert-butoxycarbonyl (Boc) protecting group enhances the stability of the compound during synthetic processes, allowing for selective reactions at the boronic acid site. Its applications extend to the development

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the introduction of the pyrazole moiety into more complex molecules, which are often explored in pharmaceutical research. The tert-butoxycarbonyl (Boc) protecting group enhances the stability of the compound during synthetic processes, allowing for selective reactions at the boronic acid site. Its applications extend to the development of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, it is used in the preparation of ligands for catalysis and materials science research, where precise molecular architecture is crucial.

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