(2-Formyl-3-methoxyphenyl)boronic acid

98%

Reagent Code: #116963
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CAS Number 958030-46-1

science Other reagents with same CAS 958030-46-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.97 g/mol
Formula C₈H₉BO₄
badge Registry Numbers
MDL Number MFCD01319042
thermostat Physical Properties
Boiling Point 408.3±55.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(2-Formyl-3-methoxyphenyl)boronic acid is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl groups. Additionally, its formyl and methoxy substituents enhance its reactivity and selectivity in complex molecular constructions. It is also employed in the development of sensors and probes due to its ability to interact with diols and other biologically relevant molecules, making it useful in biochemical research and diagnostic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,268.00
inventory 5g
10-20 days ฿12,069.00
inventory 1g
10-20 days ฿4,527.00

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(2-Formyl-3-methoxyphenyl)boronic acid
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(2-Formyl-3-methoxyphenyl)boronic acid is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl groups. Additionally, its formyl and methoxy substituents enhance its reactivity and selectivity in complex molecul

(2-Formyl-3-methoxyphenyl)boronic acid is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl groups. Additionally, its formyl and methoxy substituents enhance its reactivity and selectivity in complex molecular constructions. It is also employed in the development of sensors and probes due to its ability to interact with diols and other biologically relevant molecules, making it useful in biochemical research and diagnostic applications.

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