tert-butyl 3-cyano-3-hydroxyazetidine-1-carboxylate

98%

Reagent Code: #55306
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CAS Number 1493737-08-8

science Other reagents with same CAS 1493737-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.2191 g/mol
Formula C₉H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD21644405
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a versatile intermediate. Its structure, featuring both cyano and hydroxyl groups on an azetidine ring, makes it valuable for constructing complex molecules, particularly in the development of bioactive compounds and drug candidates. It is often employed in the synthesis of small molecule inhibitors and modulators targeting various biological pathways. Additionally, its tert-butyl ester group provides stability and ease of manipulation during chemical reactions, making it a useful building block in medicinal chemistry efforts.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,322.00

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tert-butyl 3-cyano-3-hydroxyazetidine-1-carboxylate
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This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a versatile intermediate. Its structure, featuring both cyano and hydroxyl groups on an azetidine ring, makes it valuable for constructing complex molecules, particularly in the development of bioactive compounds and drug candidates. It is often employed in the synthesis of small molecule inhibitors and modulators targeting various biological pathways. Additionally, its tert-butyl ester group provides stability

This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a versatile intermediate. Its structure, featuring both cyano and hydroxyl groups on an azetidine ring, makes it valuable for constructing complex molecules, particularly in the development of bioactive compounds and drug candidates. It is often employed in the synthesis of small molecule inhibitors and modulators targeting various biological pathways. Additionally, its tert-butyl ester group provides stability and ease of manipulation during chemical reactions, making it a useful building block in medicinal chemistry efforts.

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