tert-Butyl 3-(2-aminoethyl)-3-hydroxyazetidine-1-carboxylate

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Reagent Code: #65051
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CAS Number 1330763-29-5

science Other reagents with same CAS 1330763-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD20230540
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as a versatile intermediate. It plays a crucial role in the development of complex molecules, particularly in the synthesis of biologically active compounds. Its structure, featuring both hydroxyl and aminoethyl groups, makes it valuable for constructing heterocyclic frameworks, which are often found in drug candidates. Additionally, it is employed in the preparation of compounds targeting neurological disorders, where the azetidine ring and functional groups contribute to binding affinity and selectivity. Its tert-butyl ester group also provides stability during synthetic processes, enabling efficient transformations in multi-step reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,135.00
inventory 250mg
10-20 days ฿22,095.00

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tert-Butyl 3-(2-aminoethyl)-3-hydroxyazetidine-1-carboxylate
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This compound is primarily utilized in organic synthesis and pharmaceutical research as a versatile intermediate. It plays a crucial role in the development of complex molecules, particularly in the synthesis of biologically active compounds. Its structure, featuring both hydroxyl and aminoethyl groups, makes it valuable for constructing heterocyclic frameworks, which are often found in drug candidates. Additionally, it is employed in the preparation of compounds targeting neurological disorders, where the azetidine ring and functional groups contribute to binding affinity and selectivity. Its tert-butyl ester group also provides stability during synthetic processes, enabling efficient transformations in multi-step reactions.
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