1-(((tert-Butyldiphenylsilyl)oxy)methyl)cyclopropanol

≥95%

Reagent Code: #39775
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CAS Number 441784-82-3

science Other reagents with same CAS 441784-82-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.51 g/mol
Formula C₂₀H₂₆O₂Si
badge Registry Numbers
MDL Number MFCD09909833
thermostat Physical Properties
Boiling Point 392°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is a specialized building block in organic synthesis, featuring a tert-butyldiphenylsilyl (TBDPS)-protected hydroxymethyl group on a cyclopropanol core. The TBDPS protection shields the primary alcohol from unwanted reactions during multi-step processes, offering excellent stability under acidic, basic, and oxidative conditions. The cyclopropanol moiety acts as a reactive synthon, commonly used in ring-opening reactions (e.g., via the semi-pinacol rearrangement or homologation) to assemble complex carbocycles and heterocycles. It is particularly valuable in the total synthesis of pharmaceuticals, natural products, and bioactive molecules, allowing precise control over functional group transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,351.00
inventory 1g
10-20 days ฿40,887.00
inventory 250mg
10-20 days ฿16,362.00

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1-(((tert-Butyldiphenylsilyl)oxy)methyl)cyclopropanol
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This compound is a specialized building block in organic synthesis, featuring a tert-butyldiphenylsilyl (TBDPS)-protected hydroxymethyl group on a cyclopropanol core. The TBDPS protection shields the primary alcohol from unwanted reactions during multi-step processes, offering excellent stability under acidic, basic, and oxidative conditions. The cyclopropanol moiety acts as a reactive synthon, commonly used in ring-opening reactions (e.g., via the semi-pinacol rearrangement or homologation) to assemble

This compound is a specialized building block in organic synthesis, featuring a tert-butyldiphenylsilyl (TBDPS)-protected hydroxymethyl group on a cyclopropanol core. The TBDPS protection shields the primary alcohol from unwanted reactions during multi-step processes, offering excellent stability under acidic, basic, and oxidative conditions. The cyclopropanol moiety acts as a reactive synthon, commonly used in ring-opening reactions (e.g., via the semi-pinacol rearrangement or homologation) to assemble complex carbocycles and heterocycles. It is particularly valuable in the total synthesis of pharmaceuticals, natural products, and bioactive molecules, allowing precise control over functional group transformations.

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