(4-(2-(tert-butoxy)-2-oxoethyl)phenyl)boronic acid

95%

Reagent Code: #238614
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CAS Number 1133749-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.072 g/mol
Formula C₁₂H₁₇BO₄
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MDL Number MFCD28384338
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are key intermediates in pharmaceuticals and agrochemicals. Its boronic acid functionality allows for carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. The tert-butyl ester group enhances stability and solubility during reaction processes, and can be easily deprotected to yield carboxylic acid derivatives for further functionalization. Commonly employed in the synthesis of complex molecules where controlled reactivity and functional group tolerance are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,680.00
inventory 250mg
10-20 days ฿24,000.00
inventory 1g
10-20 days ฿48,000.00
(4-(2-(tert-butoxy)-2-oxoethyl)phenyl)boronic acid
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are key intermediates in pharmaceuticals and agrochemicals. Its boronic acid functionality allows for carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. The tert-butyl ester group enhances stability and solubility during reaction processes, and can be easily deprotected to yield carboxylic acid derivatives for further functionalization. Commonly employed in the synthesis of complex molecules where controlled reactivity and functional group tolerance are required.
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