4-Chloro-3-Fluorobenzeneboronic Acid

98%

Reagent Code: #90639
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CAS Number 137504-86-0

science Other reagents with same CAS 137504-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.37 g/mol
Formula C₆H₅BClFO₂
badge Registry Numbers
MDL Number MFCD01319010
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting various diseases. Plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Applied in the production of agrochemicals, contributing to the creation of herbicides and pesticides. Utilized in material science for the development of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs). Also employed in research laboratories for the study of boron-containing compounds and their reactivity.

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

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿1,680.00
inventory 25g
10-20 days ฿7,220.00

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4-Chloro-3-Fluorobenzeneboronic Acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting various diseases. Plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Applied in the production of agrochemicals, contributing to the creation of herbicides and pesticides. Utilized in material science for the development of organic electronic materials, such as semiconductors and light-emitting diodes (

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting various diseases. Plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Applied in the production of agrochemicals, contributing to the creation of herbicides and pesticides. Utilized in material science for the development of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs). Also employed in research laboratories for the study of boron-containing compounds and their reactivity.

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