5-(((Tert-Butyldimethylsilyl)Oxy)Methyl)Pyrrolidin-2-One

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Reagent Code: #63706
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CAS Number 177911-57-8

science Other reagents with same CAS 177911-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.39 g/mol
Formula C₁₁H₂₃NO₂Si
badge Registry Numbers
MDL Number MFCD23135503
thermostat Physical Properties
Boiling Point 307.6±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.942±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This compound is a protected derivative of 5-(hydroxymethyl)pyrrolidin-2-one, featuring a tert-butyldimethylsilyl (TBDMS) ether protecting group on the primary hydroxyl. The TBDMS protection enables selective functionalization of the pyrrolidin-2-one core during multi-step organic synthesis, preserving the alcohol while other transformations occur. It is particularly valuable in pharmaceutical and natural product synthesis, where precise control over functional groups is essential. The pyrrolidin-2-one moiety acts as a versatile building block for more complex heterocycles, serving as a key intermediate in drug development. Its robustness across diverse reaction conditions supports use in elaborate synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,860.00
inventory 250mg
10-20 days ฿9,450.00
inventory 1g
10-20 days ฿18,900.00
5-(((Tert-Butyldimethylsilyl)Oxy)Methyl)Pyrrolidin-2-One
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This compound is a protected derivative of 5-(hydroxymethyl)pyrrolidin-2-one, featuring a tert-butyldimethylsilyl (TBDMS) ether protecting group on the primary hydroxyl. The TBDMS protection enables selective functionalization of the pyrrolidin-2-one core during multi-step organic synthesis, preserving the alcohol while other transformations occur. It is particularly valuable in pharmaceutical and natural product synthesis, where precise control over functional groups is essential. The pyrrolidin-2-one m

This compound is a protected derivative of 5-(hydroxymethyl)pyrrolidin-2-one, featuring a tert-butyldimethylsilyl (TBDMS) ether protecting group on the primary hydroxyl. The TBDMS protection enables selective functionalization of the pyrrolidin-2-one core during multi-step organic synthesis, preserving the alcohol while other transformations occur. It is particularly valuable in pharmaceutical and natural product synthesis, where precise control over functional groups is essential. The pyrrolidin-2-one moiety acts as a versatile building block for more complex heterocycles, serving as a key intermediate in drug development. Its robustness across diverse reaction conditions supports use in elaborate synthetic routes.

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