(4-Chloro-3-methoxyphenyl)boronic acid

98%

Reagent Code: #90642
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CAS Number 89694-47-3

science Other reagents with same CAS 89694-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.4 g/mol
Formula C₇H₈BClO₃
badge Registry Numbers
MDL Number MFCD01318965
thermostat Physical Properties
Boiling Point 341.651°C
inventory_2 Storage & Handling
Density 1.325g/mL
Storage room temperature, dry

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of complex organic molecules. This compound is also utilized in the development of bioactive compounds and materials for electronic devices due to its boronic acid functionality, which allows for versatile chemical transformations. Additionally, it serves as a building block in the synthesis of ligands for catalysis and in the creation of sensors for detecting specific analytes.

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inventory 25g
10-20 days ฿8,928.00

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(4-Chloro-3-methoxyphenyl)boronic acid
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Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of complex organic molecules. This compound is also utilized in the development of bioactive compounds and materials for electronic devices due to its boronic acid functionality, which allows for versatile chemical transformations. Additionally, it se

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of complex organic molecules. This compound is also utilized in the development of bioactive compounds and materials for electronic devices due to its boronic acid functionality, which allows for versatile chemical transformations. Additionally, it serves as a building block in the synthesis of ligands for catalysis and in the creation of sensors for detecting specific analytes.

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