(3-Chloro-2-fluorophenyl)boronic acid

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Reagent Code: #90195
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CAS Number 352535-82-1

science Other reagents with same CAS 352535-82-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.37 g/mol
Formula C₆H₅BClFO₂
thermostat Physical Properties
Melting Point 223°C
Boiling Point 315.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(3-Chloro-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of biologically active compounds and in the modification of organic frameworks for material science applications. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿540.00
inventory 5g
10-20 days ฿1,780.00
inventory 25g
10-20 days ฿6,450.00
inventory 100g
10-20 days ฿19,800.00

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(3-Chloro-2-fluorophenyl)boronic acid
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(3-Chloro-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in drug discovery and development. Additionally, i

(3-Chloro-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of biologically active compounds and in the modification of organic frameworks for material science applications. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.

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