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

95%

Reagent Code: #181130
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CAS Number 114653-18-8

science Other reagents with same CAS 114653-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.16 g/mol
Formula C₁₆H₂₃BO₃
badge Registry Numbers
MDL Number MFCD30183597
thermostat Physical Properties
Boiling Point 327.2±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.01±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

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 palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The allylic benzyl ether moiety allows for further functionalization or deprotection, adding versatility in multi-step synthetic routes. Commonly employed in the preparation of bioactive compounds and conjugated systems for materials science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,990.00
inventory 1g
10-20 days ฿13,300.00
inventory 5g
10-20 days ฿47,880.00

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(E)-2-(3-(Benzyloxy)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. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The allylic benzyl ether moiety allows for further functionalization or deprotection, adding versatility in multi-step synthetic routes. Commonly employed in the preparation of bioactive

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 palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The allylic benzyl ether moiety allows for further functionalization or deprotection, adding versatility in multi-step synthetic routes. Commonly employed in the preparation of bioactive compounds and conjugated systems for materials science.

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