tert-Butyl 2-cyanoazetidine-1-carboxylate

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Reagent Code: #43100
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CAS Number 887588-82-1

science Other reagents with same CAS 887588-82-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.2200 g/mol
Formula C₉H₁₄N₂O₂
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description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of drug candidates, where the azetidine ring structure is of interest due to its conformational rigidity and potential biological activity. The tert-butyl group provides steric protection, while the cyano group can be further modified or participate in various chemical reactions, making it a useful intermediate in medicinal chemistry and peptide synthesis. Additionally, it may be employed in the synthesis of agrochemicals and other fine chemicals, where the azetidine scaffold is a key structural component.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,610.00
inventory 100mg
10-20 days ฿4,310.00
inventory 1g
10-20 days ฿25,570.00
inventory 250mg
10-20 days ฿7,360.00

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tert-Butyl 2-cyanoazetidine-1-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of drug candidates, where the azetidine ring structure is of interest due to its conformational rigidity and potential biological activity. The tert-butyl group provides steric protection, while the cyano group can be further modified or participate in various chemical reactions, making it a use

This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of drug candidates, where the azetidine ring structure is of interest due to its conformational rigidity and potential biological activity. The tert-butyl group provides steric protection, while the cyano group can be further modified or participate in various chemical reactions, making it a useful intermediate in medicinal chemistry and peptide synthesis. Additionally, it may be employed in the synthesis of agrochemicals and other fine chemicals, where the azetidine scaffold is a key structural component.

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