3-Chloro-5-fluorobenzeneboronic acid

98%

Reagent Code: #90215
label
Alias 3-Chloro-5-fluorophenylboronic acid
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CAS Number 328956-61-2

science Other reagents with same CAS 328956-61-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.37 g/mol
Formula C₆H₅BClFO₂
badge Registry Numbers
MDL Number MFCD06801741
thermostat Physical Properties
Melting Point >200°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in the pharmaceutical industry. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various biologically active molecules. It is also employed in the development of agrochemicals and materials science, where it contributes to the creation of advanced polymers and functional materials. Its halogen substituents enhance reactivity and selectivity in coupling reactions, making it a valuable reagent in medicinal chemistry for drug discovery and development.

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Test Parameter Specification
Purity 98-100
Appearance White to off-white crystal
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿2,700.00
inventory 25g
10-20 days ฿11,630.00

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3-Chloro-5-fluorobenzeneboronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in the pharmaceutical industry. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various biologically active molecules. It is also employed in the development of agrochemicals and materials science, where it contributes to the creation of advanced polymers and fu

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic compounds, especially in the pharmaceutical industry. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of various biologically active molecules. It is also employed in the development of agrochemicals and materials science, where it contributes to the creation of advanced polymers and functional materials. Its halogen substituents enhance reactivity and selectivity in coupling reactions, making it a valuable reagent in medicinal chemistry for drug discovery and development.

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