(5-Chloro-2,4-difluorophenyl)boronic acid

95%

Reagent Code: #113342
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CAS Number 911645-24-4

science Other reagents with same CAS 911645-24-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.36 g/mol
Formula C₆H₄BClF₂O₂
badge Registry Numbers
MDL Number MFCD04038751
thermostat Physical Properties
Boiling Point 297.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(5-Chloro-2,4-difluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its specific structure allows for the introduction of chloro and fluoro substituents into complex molecules, enhancing their biological activity or chemical properties. Additionally, it serves as a building block in the development of boron-based compounds for applications in medicinal chemistry, such as enzyme inhibitors or drug candidates. Its stability and reactivity make it a versatile reagent in research and industrial processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿17,685.00
inventory 100mg
10-20 days ฿1,179.00
inventory 250mg
10-20 days ฿1,971.00
inventory 1g
10-20 days ฿4,851.00

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(5-Chloro-2,4-difluorophenyl)boronic acid
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(5-Chloro-2,4-difluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its specific structure allows for the introduction of chloro and fluoro substituents into complex molecules, enhancing their biological activity or chemical properties. Additionally, it serves as a building block in t

(5-Chloro-2,4-difluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its specific structure allows for the introduction of chloro and fluoro substituents into complex molecules, enhancing their biological activity or chemical properties. Additionally, it serves as a building block in the development of boron-based compounds for applications in medicinal chemistry, such as enzyme inhibitors or drug candidates. Its stability and reactivity make it a versatile reagent in research and industrial processes.

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