tert-Butyl 3-acetoxyazetidine-1-carboxylate

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Reagent Code: #44757
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CAS Number 1215205-53-0

science Other reagents with same CAS 1215205-53-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.25 g/mol
Formula C₁₀H₁₇NO₄
badge Registry Numbers
MDL Number MFCD24445131
thermostat Physical Properties
Boiling Point 269.0±33.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used primarily in organic synthesis as a versatile intermediate, this compound is often employed in the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both an acetoxy group and a tert-butyl carboxylate, makes it valuable for constructing azetidine-containing compounds, which are of interest due to their biological activity. It is also utilized in the development of prodrugs and as a protective group in peptide synthesis, enabling selective reactions in multi-step processes. Additionally, its stability and reactivity make it suitable for use in medicinal chemistry for the design of new drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,673.00
inventory 100mg
10-20 days ฿531.00
inventory 250mg
10-20 days ฿891.00

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tert-Butyl 3-acetoxyazetidine-1-carboxylate
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Used primarily in organic synthesis as a versatile intermediate, this compound is often employed in the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both an acetoxy group and a tert-butyl carboxylate, makes it valuable for constructing azetidine-containing compounds, which are of interest due to their biological activity. It is also utilized in the development of prodrugs and as a protective group in peptide synthesis, enabling selective reactions in

Used primarily in organic synthesis as a versatile intermediate, this compound is often employed in the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both an acetoxy group and a tert-butyl carboxylate, makes it valuable for constructing azetidine-containing compounds, which are of interest due to their biological activity. It is also utilized in the development of prodrugs and as a protective group in peptide synthesis, enabling selective reactions in multi-step processes. Additionally, its stability and reactivity make it suitable for use in medicinal chemistry for the design of new drug candidates.

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