(E)-2-(3,4-dimethoxystyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Reagent Code: #183991
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CAS Number 1618099-49-2

science Other reagents with same CAS 1618099-49-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.17 g/mol
Formula C₁₆H₂₃BO₄
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. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical, agrochemical, and materials science research. Particularly useful for constructing stilbene derivatives and conjugated systems found in fluorescent dyes, organic semiconductors, and bioactive compounds. The (E)-configuration ensures geometric precision in the final product, which is critical for desired optical or biological properties. Stable and compatible with various functional groups, it supports efficient and selective synthetic routes in both academic and industrial settings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,580.00
inventory 5g
10-20 days ฿51,020.00
inventory 500mg
10-20 days ฿10,940.00
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(E)-2-(3,4-dimethoxystyryl)-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. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical, agrochemical, and materials science research. Particularly useful for constructing stilbene derivatives and conjugated systems found in fluorescent dyes, organic semiconductors, and bioactive compounds. The

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. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical, agrochemical, and materials science research. Particularly useful for constructing stilbene derivatives and conjugated systems found in fluorescent dyes, organic semiconductors, and bioactive compounds. The (E)-configuration ensures geometric precision in the final product, which is critical for desired optical or biological properties. Stable and compatible with various functional groups, it supports efficient and selective synthetic routes in both academic and industrial settings.

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