2-(2-(2-methoxyphenyl)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

97%

Reagent Code: #209579
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CAS Number 1398771-25-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.17 g/mol
Formula C₁₆H₂₃BO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. This specific boronate ester transfers the 2-(2-methoxyphenyl)prop-1-en-1-yl group, making it particularly valuable in pharmaceutical and agrochemical industries for constructing substituted styrene derivatives and related structures. Its boronate ester group facilitates efficient and selective coupling under mild conditions. Commonly employed in research and development of functional materials, including organic semiconductors and liquid crystals.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,970.00
1g
10-20 days ฿20,650.00
5g
10-20 days ฿56,580.00
2-(2-(2-methoxyphenyl)prop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. This specific boronate ester transfers the 2-(2-methoxyphenyl)prop-1-en-1-yl group, making it particularly valuable in pharmaceutical and agrochemical industries for constructing substituted styrene derivatives and related structures. Its boronate ester group facilitates efficient and selective coupling under mild conditions. Commonly employed in
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. This specific boronate ester transfers the 2-(2-methoxyphenyl)prop-1-en-1-yl group, making it particularly valuable in pharmaceutical and agrochemical industries for constructing substituted styrene derivatives and related structures. Its boronate ester group facilitates efficient and selective coupling under mild conditions. Commonly employed in research and development of functional materials, including organic semiconductors and liquid crystals.
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