tert-butyldimethyl(4-(prop-1-en-2-yl)phenoxy)silane

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Reagent Code: #242178
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CAS Number 129181-43-7

science Other reagents with same CAS 129181-43-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.44 g/mol
Formula C₁₅H₂₄OSi
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

tert-Butyldimethyl(4-(prop-1-en-2-yl)phenoxy)silane is a silyl ether serving as a protected intermediate in organic synthesis. It features the tert-butyldimethylsilyl (TBDMS) group attached to the phenolic oxygen of 4-(prop-1-en-2-yl)phenol, offering high stability and selectivity under diverse reaction conditions. This protection enables precise manipulation of the isopropenyl moiety for further functionalization, such as in coupling reactions or as a directing group, while safeguarding the phenolic hydroxyl. The TBDMS group can be selectively introduced and removed under mild conditions (e.g., using fluoride ions or mild acids), facilitating control in multi-step syntheses of complex molecules like natural products, pharmaceuticals, steroids, prostaglandins, and other bioactive compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,210.00
inventory 5g
10-20 days ฿23,290.00

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tert-butyldimethyl(4-(prop-1-en-2-yl)phenoxy)silane
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tert-Butyldimethyl(4-(prop-1-en-2-yl)phenoxy)silane is a silyl ether serving as a protected intermediate in organic synthesis. It features the tert-butyldimethylsilyl (TBDMS) group attached to the phenolic oxygen of 4-(prop-1-en-2-yl)phenol, offering high stability and selectivity under diverse reaction conditions. This protection enables precise manipulation of the isopropenyl moiety for further functionalization, such as in coupling reactions or as a directing group, while safeguarding the phenolic hyd

tert-Butyldimethyl(4-(prop-1-en-2-yl)phenoxy)silane is a silyl ether serving as a protected intermediate in organic synthesis. It features the tert-butyldimethylsilyl (TBDMS) group attached to the phenolic oxygen of 4-(prop-1-en-2-yl)phenol, offering high stability and selectivity under diverse reaction conditions. This protection enables precise manipulation of the isopropenyl moiety for further functionalization, such as in coupling reactions or as a directing group, while safeguarding the phenolic hydroxyl. The TBDMS group can be selectively introduced and removed under mild conditions (e.g., using fluoride ions or mild acids), facilitating control in multi-step syntheses of complex molecules like natural products, pharmaceuticals, steroids, prostaglandins, and other bioactive compounds.

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