tert-Butyl3-(2-(tosyloxy)ethyl)azetidine-1-carboxylate

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Reagent Code: #155407
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CAS Number 676125-83-0

science Other reagents with same CAS 676125-83-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.45 g/mol
Formula C₁₇H₂₅NO₅S
badge Registry Numbers
MDL Number MFCD31555485
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where the azetidine ring serves as a structural scaffold. The tosylate group acts as a good leaving group, enabling nucleophilic substitution reactions to introduce various functional groups. The tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity by shielding the nitrogen during multi-step syntheses. Commonly applied in medicinal chemistry for constructing nitrogen-containing heterocycles with potential biological activity.

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inventory 100mg
10-20 days ฿6,180.00

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tert-Butyl3-(2-(tosyloxy)ethyl)azetidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where the azetidine ring serves as a structural scaffold. The tosylate group acts as a good leaving group, enabling nucleophilic substitution reactions to introduce various functional groups. The tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity by shielding the nitrogen during multi-step syntheses. Commonly applied in medicinal chemistr

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where the azetidine ring serves as a structural scaffold. The tosylate group acts as a good leaving group, enabling nucleophilic substitution reactions to introduce various functional groups. The tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity by shielding the nitrogen during multi-step syntheses. Commonly applied in medicinal chemistry for constructing nitrogen-containing heterocycles with potential biological activity.

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