(E)-(2-(3-Methoxy-3-oxoprop-1-en-1-yl)phenyl)boronic acid

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Reagent Code: #185265
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CAS Number 372193-68-5

science Other reagents with same CAS 372193-68-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206 g/mol
Formula C₁₀H₁₁BO₄
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MDL Number MFCD02179475
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in creating complex aromatic systems. The α,β-unsaturated ester moiety allows for further functionalization, such as Michael additions or reduction, expanding its utility in synthesizing bioactive molecules. Commonly employed in the preparation of conjugated materials and intermediates for drug discovery research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,160.00
inventory 5g
10-20 days ฿21,190.00
inventory 25g
10-20 days ฿105,910.00
inventory 1g
10-20 days ฿4,250.00

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(E)-(2-(3-Methoxy-3-oxoprop-1-en-1-yl)phenyl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in creating complex aromatic systems. The α,β-unsaturated ester moiety allows for further functionalization, such as Michael additions or reduction, expanding its utility in synthesizing bioactive molecules. Commonly emplo

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in creating complex aromatic systems. The α,β-unsaturated ester moiety allows for further functionalization, such as Michael additions or reduction, expanding its utility in synthesizing bioactive molecules. Commonly employed in the preparation of conjugated materials and intermediates for drug discovery research.

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