tert-Butyl N-spiro[2.4]heptan-1-ylcarbamate

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Reagent Code: #75930
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CAS Number 1774896-53-5

science Other reagents with same CAS 1774896-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.3 g/mol
Formula C₁₂H₂₁NO₂
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MDL Number MFCD27995717
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. Its unique spirocyclic structure makes it valuable in the development of pharmaceuticals, particularly in the creation of compounds with potential biological activity. The tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule without interference. This compound is often employed in medicinal chemistry research to explore new drug candidates, especially in the design of molecules targeting neurological or metabolic disorders. Its stability and reactivity profile make it a useful intermediate in the synthesis of heterocyclic compounds, which are frequently found in active pharmaceutical ingredients.

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inventory 1g
10-20 days ฿225,300.00

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tert-Butyl N-spiro[2.4]heptan-1-ylcarbamate
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This chemical is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. Its unique spirocyclic structure makes it valuable in the development of pharmaceuticals, particularly in the creation of compounds with potential biological activity. The tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule without interference. This compound is often employed in medicinal chemistry

This chemical is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. Its unique spirocyclic structure makes it valuable in the development of pharmaceuticals, particularly in the creation of compounds with potential biological activity. The tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule without interference. This compound is often employed in medicinal chemistry research to explore new drug candidates, especially in the design of molecules targeting neurological or metabolic disorders. Its stability and reactivity profile make it a useful intermediate in the synthesis of heterocyclic compounds, which are frequently found in active pharmaceutical ingredients.

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