(3-Methoxy-2-methylphenyl)boronic acid

97%

Reagent Code: #118158
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CAS Number 1313617-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.98 g/mol
Formula C₈H₁₁BO₃
badge Registry Numbers
MDL Number MFCD18398348
thermostat Physical Properties
Boiling Point 325.8±52.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

(3-Methoxy-2-methylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. 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 is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in biochemical and analytical applications. Its stability and reactivity also make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,152.00
inventory 250mg
10-20 days ฿1,998.00
inventory 1g
10-20 days ฿6,480.00
(3-Methoxy-2-methylphenyl)boronic acid
(3-Methoxy-2-methylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. 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 is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in biochemical and analytical applications. Its stability and reactivity also make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive compounds.
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