3-Bromo-2-(2'-chlorobenzyloxy)-5-methylphenylboronic acid(contains varying amounts of Anhydride)

95%

Reagent Code: #117951
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CAS Number 849052-17-1

science Other reagents with same CAS 849052-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.4 g/mol
Formula C₁₄H₁₃BBrClO₃
badge Registry Numbers
MDL Number MFCD06411364
thermostat Physical Properties
Melting Point 123-128 °C(lit.)
Boiling Point 514.5±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.54±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, the presence of the chlorobenzyloxy and methyl groups enhances its reactivity and selectivity in various chemical transformations. The varying amounts of anhydride in the compound can influence its stability and reactivity, requiring careful handling in synthetic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,141.00
inventory 5g
10-20 days ฿35,091.00
inventory 1g
10-20 days ฿8,361.00

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3-Bromo-2-(2'-chlorobenzyloxy)-5-methylphenylboronic acid(contains varying amounts of Anhydride)
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, the presence of the chlorobenzyloxy and methyl groups enhances its reactivity and selectivity in va

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, the presence of the chlorobenzyloxy and methyl groups enhances its reactivity and selectivity in various chemical transformations. The varying amounts of anhydride in the compound can influence its stability and reactivity, requiring careful handling in synthetic applications.

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