(E)-2-(3-(Trimethylsilyl)allyl)-1,3,6,2-dioxazaborocane

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Reagent Code: #185369
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CAS Number 774597-13-6

science Other reagents with same CAS 774597-13-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.18 g/mol
Formula C₁₀H₂₂BNO₂Si
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions where the trimethylsilyl group acts as a stabilizing and directing moiety. The boron-containing ring enables participation in Suzuki-Miyaura coupling reactions, allowing for efficient carbon-carbon bond formation in complex molecule assembly. Its allylic structure with defined stereochemistry (E-configuration) supports stereoselective transformations, making it valuable in pharmaceutical and agrochemical synthesis where precise molecular architecture is critical. The silyl group also facilitates purification and handling due to enhanced lipophilicity and stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,600.00
inventory 1g
10-20 days ฿7,010.00
inventory 5g
10-20 days ฿26,520.00

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(E)-2-(3-(Trimethylsilyl)allyl)-1,3,6,2-dioxazaborocane
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Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions where the trimethylsilyl group acts as a stabilizing and directing moiety. The boron-containing ring enables participation in Suzuki-Miyaura coupling reactions, allowing for efficient carbon-carbon bond formation in complex molecule assembly. Its allylic structure with defined stereochemistry (E-configuration) supports stereoselective transformations, making it valuable in pharmaceutical and agrochemical synthesi

Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions where the trimethylsilyl group acts as a stabilizing and directing moiety. The boron-containing ring enables participation in Suzuki-Miyaura coupling reactions, allowing for efficient carbon-carbon bond formation in complex molecule assembly. Its allylic structure with defined stereochemistry (E-configuration) supports stereoselective transformations, making it valuable in pharmaceutical and agrochemical synthesis where precise molecular architecture is critical. The silyl group also facilitates purification and handling due to enhanced lipophilicity and stability under various reaction conditions.

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