3-(4'-Methoxybenzyloxy)phenylboronic acid(contains varying amounts of Anhydride)

95%

Reagent Code: #213291
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CAS Number 1072951-89-3

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.08 g/mol
Formula C₁₄H₁₅BO₄
thermostat Physical Properties
Melting Point 159-163 °C
inventory_2 Storage & Handling
Storage Room temperature

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 functionality allows for selective transformations under mild conditions, making it valuable in the preparation of complex aromatic and biaryl compounds. Commonly employed in research settings for the synthesis of functionalized benzyl ethers and in the development of bioactive molecules. The presence of anhydride forms may influence reactivity, requiring controlled conditions during use.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿13,100.00
3-(4'-Methoxybenzyloxy)phenylboronic acid(contains varying amounts of Anhydride)
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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 functionality allows for selective transformations under mild conditions, making it valuable in the preparation of complex aromatic and biaryl compounds. Commonly employed in research settings for the synthesis of functionalized benzyl ethers and in the development of bioactive molecules. The presence of a

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 functionality allows for selective transformations under mild conditions, making it valuable in the preparation of complex aromatic and biaryl compounds. Commonly employed in research settings for the synthesis of functionalized benzyl ethers and in the development of bioactive molecules. The presence of anhydride forms may influence reactivity, requiring controlled conditions during use.

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