(3-Chloro-5-methylphenyl)boronic acid

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Reagent Code: #89151
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CAS Number 913836-14-3

science Other reagents with same CAS 913836-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.4 g/mol
Formula C₇H₈BClO₂
thermostat Physical Properties
Melting Point 235-238°C
Boiling Point 336.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(3-Chloro-5-methylphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it finds applications in material science for the development of organic electronic materials and polymers. Its stability and reactivity make it a valuable building block in the preparation of advanced materials and fine chemicals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿531.00
inventory 1g
10-20 days ฿1,287.00
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(3-Chloro-5-methylphenyl)boronic acid
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(3-Chloro-5-methylphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it finds a

(3-Chloro-5-methylphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it finds applications in material science for the development of organic electronic materials and polymers. Its stability and reactivity make it a valuable building block in the preparation of advanced materials and fine chemicals.

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