Ethyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylate

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Reagent Code: #182699
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CAS Number 676560-15-9

science Other reagents with same CAS 676560-15-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.48 g/mol
Formula C₁₅H₃₀O₃Si
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and complex natural products. Its silyl-protected hydroxyl group allows selective reactivity, making it valuable in multi-step syntheses where functional group compatibility is critical. Commonly employed in the development of steroidal analogs and bioactive molecules due to the stability and ease of deprotection of the TBS group. The ester functionality enables further transformations such as reduction to alcohols or conversion to amides, supporting its role in building molecular complexity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,820.00
inventory 50mg
10-20 days ฿1,020.00
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Ethyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and complex natural products. Its silyl-protected hydroxyl group allows selective reactivity, making it valuable in multi-step syntheses where functional group compatibility is critical. Commonly employed in the development of steroidal analogs and bioactive molecules due to the stability and ease of deprotection of the TBS group. The ester functionality enables further transformations such as reduction to

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and complex natural products. Its silyl-protected hydroxyl group allows selective reactivity, making it valuable in multi-step syntheses where functional group compatibility is critical. Commonly employed in the development of steroidal analogs and bioactive molecules due to the stability and ease of deprotection of the TBS group. The ester functionality enables further transformations such as reduction to alcohols or conversion to amides, supporting its role in building molecular complexity.

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