tert-Butyl ((3-oxocyclopentyl)methyl)carbamate

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Reagent Code: #124596
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CAS Number 1260674-55-2

science Other reagents with same CAS 1260674-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.27 g/mol
Formula C₁₁H₁₉NO₃
badge Registry Numbers
MDL Number MFCD16036451
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis as a protective group for amines. It is particularly valuable in peptide synthesis, where it helps prevent unwanted reactions at the amine group during complex molecule construction. The tert-butyl group provides stability under various reaction conditions, making it suitable for multi-step synthetic processes. Additionally, it can be selectively removed under mild acidic conditions, allowing for the controlled deprotection of the amine group when needed. Its application extends to the development of pharmaceuticals, where it aids in the synthesis of intermediates for drug molecules. The compound’s structure also makes it useful in the preparation of cyclopentane derivatives, which are often found in bioactive compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,403.00
inventory 100mg
10-20 days ฿6,084.00
inventory 1g
10-20 days ฿22,815.00

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tert-Butyl ((3-oxocyclopentyl)methyl)carbamate
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This chemical is primarily used in organic synthesis as a protective group for amines. It is particularly valuable in peptide synthesis, where it helps prevent unwanted reactions at the amine group during complex molecule construction. The tert-butyl group provides stability under various reaction conditions, making it suitable for multi-step synthetic processes. Additionally, it can be selectively removed under mild acidic conditions, allowing for the controlled deprotection of the amine group when need

This chemical is primarily used in organic synthesis as a protective group for amines. It is particularly valuable in peptide synthesis, where it helps prevent unwanted reactions at the amine group during complex molecule construction. The tert-butyl group provides stability under various reaction conditions, making it suitable for multi-step synthetic processes. Additionally, it can be selectively removed under mild acidic conditions, allowing for the controlled deprotection of the amine group when needed. Its application extends to the development of pharmaceuticals, where it aids in the synthesis of intermediates for drug molecules. The compound’s structure also makes it useful in the preparation of cyclopentane derivatives, which are often found in bioactive compounds.

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