Tert-butyldimethyl((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl)oxy)silane

98%

Reagent Code: #57696
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CAS Number 865869-27-8

science Other reagents with same CAS 865869-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.37 g/mol
Formula C₁₈H₃₅BO₃Si
badge Registry Numbers
MDL Number MFCD11618142
inventory_2 Storage & Handling
Storage -20°C, store under inert gas

description Product Description

This compound is primarily used in organic synthesis as a protecting group for alcohols and as a key intermediate in the preparation of complex molecules. Its silicon-based structure allows it to selectively protect hydroxyl groups during multi-step reactions, ensuring that specific functional groups remain unaffected. Additionally, the boronate ester moiety in the molecule makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a versatile tool in the development of novel organic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,212.00
inventory 250mg
10-20 days ฿7,920.00
inventory 1g
10-20 days ฿19,692.00

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Tert-butyldimethyl((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl)oxy)silane
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This compound is primarily used in organic synthesis as a protecting group for alcohols and as a key intermediate in the preparation of complex molecules. Its silicon-based structure allows it to selectively protect hydroxyl groups during multi-step reactions, ensuring that specific functional groups remain unaffected. Additionally, the boronate ester moiety in the molecule makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a versatile tool in the development of novel organic compounds.
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