Tert-Butyldimethyl((2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Allyl)Oxy)Silane

97%

Reagent Code: #243689
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CAS Number 350498-98-5

science Other reagents with same CAS 350498-98-5

blur_circular Chemical Specifications

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Weight 298.3 g/mol
Formula C₁₅H₃₁BO₃Si
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a bifunctional coupling agent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The compound contains both a boronate ester and a silyl-protected allyl alcohol moiety, enabling sequential or selective transformations. It serves as a versatile building block for introducing allyl functionalities in complex molecule synthesis, especially in pharmaceuticals and agrochemicals. The silyl ether group provides stability and chemoselectivity during reaction sequences, while the boronate group allows for palladium-catalyzed carbon-carbon bond formation. Commonly applied in the synthesis of bioactive molecules and functional materials where controlled reactivity and orthogonal protection are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,980.00
inventory 250mg
10-20 days ฿11,700.00
inventory 1g
10-20 days ฿24,620.00

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Tert-Butyldimethyl((2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Allyl)Oxy)Silane
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Used as a bifunctional coupling agent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The compound contains both a boronate ester and a silyl-protected allyl alcohol moiety, enabling sequential or selective transformations. It serves as a versatile building block for introducing allyl functionalities in complex molecule synthesis, especially in pharmaceuticals and agrochemicals. The silyl ether group provides stability and chemoselectivity during reaction sequences, while the boronate group allows for palladium-catalyzed carbon-carbon bond formation. Commonly applied in the synthesis of bioactive molecules and functional materials where controlled reactivity and orthogonal protection are required.
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