(4-(2-Methoxy-2-oxoethoxy)phenyl)boronic acid

98%

Reagent Code: #203105
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CAS Number 957063-00-2

science Other reagents with same CAS 957063-00-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.99 g/mol
Formula C₉H₁₁BO₅
badge Registry Numbers
MDL Number MFCD09878347
thermostat Physical Properties
Boiling Point 372.9 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.26 g/cm3
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for pharmaceutical and agrochemical development. Its boronic acid functional group allows for mild, selective coupling with aryl halides, making it valuable in constructing biaryl compounds. The presence of a methoxyacetate ester offers a handle for further functionalization or hydrolysis to a carboxylic acid. Commonly applied in the synthesis of complex molecules where modular assembly and functional group tolerance are essential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,260.00
inventory 250mg
10-20 days ฿3,820.00
inventory 1g
10-20 days ฿10,300.00
(4-(2-Methoxy-2-oxoethoxy)phenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for pharmaceutical and agrochemical development. Its boronic acid functional group allows for mild, selective coupling with aryl halides, making it valuable in constructing biaryl compounds. The presence of a methoxyacetate ester offers a handle for further functionalization or hydrolysis to a carboxylic acid. Commonly applied in the synthesis of complex molecules where modula

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for pharmaceutical and agrochemical development. Its boronic acid functional group allows for mild, selective coupling with aryl halides, making it valuable in constructing biaryl compounds. The presence of a methoxyacetate ester offers a handle for further functionalization or hydrolysis to a carboxylic acid. Commonly applied in the synthesis of complex molecules where modular assembly and functional group tolerance are essential.

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