tert-Butyl 3-(dimethylamino)azetidine-1-carboxylate

≥95%

Reagent Code: #132652
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CAS Number 792970-55-9

science Other reagents with same CAS 792970-55-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.28 g/mol
Formula C₁₀H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD09264498
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized azetidine rings. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the production of kinase inhibitors and central nervous system agents due to the azetidine scaffold’s favorable metabolic stability and solubility properties. The dimethylamino group enables further alkylation or quaternization, facilitating the creation of diverse compound libraries for drug discovery. Also utilized in the preparation of protease inhibitors and antiviral agents.

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inventory 1g
10-20 days ฿27,460.00

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tert-Butyl 3-(dimethylamino)azetidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized azetidine rings. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the production of kinase inhibitors and central nervous system agents due to the azetidine scaffold’s favorable metabolic stability and solubility properties. The dimethylamino group enables further alkylation or

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized azetidine rings. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the production of kinase inhibitors and central nervous system agents due to the azetidine scaffold’s favorable metabolic stability and solubility properties. The dimethylamino group enables further alkylation or quaternization, facilitating the creation of diverse compound libraries for drug discovery. Also utilized in the preparation of protease inhibitors and antiviral agents.

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