(3-Chloro-2-methylphenyl)boronic acid

98%

Reagent Code: #90196
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CAS Number 313545-20-9

science Other reagents with same CAS 313545-20-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.4 g/mol
Formula C₇H₈BClO₂
thermostat Physical Properties
Boiling Point 325.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis as a key intermediate for cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables selective reactions with halides or triflates, making it essential for creating complex organic molecules. Additionally, it finds applications in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿333.00
inventory 1g
10-20 days ฿567.00
inventory 5g
10-20 days ฿2,430.00
inventory 25g
10-20 days ฿9,522.00

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(3-Chloro-2-methylphenyl)boronic acid
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Used primarily in organic synthesis as a key intermediate for cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables selective reactions with halides or triflates, making it essential for creating complex organic molecules. Additionally, it finds applications in the development of sensors and molecular recognition systems due to its ability to interac

Used primarily in organic synthesis as a key intermediate for cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables selective reactions with halides or triflates, making it essential for creating complex organic molecules. Additionally, it finds applications in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups.

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