2-(t-Butyldimethylsilyloxy)Ethanamine

95%

Reagent Code: #88193
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CAS Number 101711-55-1

science Other reagents with same CAS 101711-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.344 g/mol
Formula C₈H₂₁NOSi
badge Registry Numbers
MDL Number MFCD18206132
inventory_2 Storage & Handling
Storage 2~8℃,Seal

description Product Description

2-(t-Butyldimethylsilyloxy)ethanamine is a protected derivative of ethanolamine, where the hydroxyl group is shielded by the t-butyldimethylsilyl (TBDMS) protecting group, leaving the primary amine free. It serves as a versatile building block in organic synthesis for constructing complex molecules, including pharmaceuticals, natural products, and peptides. The TBDMS protection prevents interference from the hydroxyl during reactions at the amine or other functional groups, enabling selective transformations. The protecting group is readily removed under mild acidic or fluoride conditions to reveal the free hydroxyl. This reagent is prized for its stability across diverse reaction conditions and broad compatibility with common synthetic reagents.

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Test Parameter Specification
Purity 94.5-100
Appearance Colorless to almost colorless clear liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1ml
10-20 days ฿500.00
inventory 5ml
10-20 days ฿1,880.00
inventory 25ml
10-20 days ฿7,100.00

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2-(t-Butyldimethylsilyloxy)Ethanamine
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2-(t-Butyldimethylsilyloxy)ethanamine is a protected derivative of ethanolamine, where the hydroxyl group is shielded by the t-butyldimethylsilyl (TBDMS) protecting group, leaving the primary amine free. It serves as a versatile building block in organic synthesis for constructing complex molecules, including pharmaceuticals, natural products, and peptides. The TBDMS protection prevents interference from the hydroxyl during reactions at the amine or other functional groups, enabling selective transformation
2-(t-Butyldimethylsilyloxy)ethanamine is a protected derivative of ethanolamine, where the hydroxyl group is shielded by the t-butyldimethylsilyl (TBDMS) protecting group, leaving the primary amine free. It serves as a versatile building block in organic synthesis for constructing complex molecules, including pharmaceuticals, natural products, and peptides. The TBDMS protection prevents interference from the hydroxyl during reactions at the amine or other functional groups, enabling selective transformations. The protecting group is readily removed under mild acidic or fluoride conditions to reveal the free hydroxyl. This reagent is prized for its stability across diverse reaction conditions and broad compatibility with common synthetic reagents.
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