tert-Butyl 3-(2-bromoethyl)azetidine-1-carboxylate

≥95%

Reagent Code: #117397
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CAS Number 1420859-80-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.16 g/mol
Formula C₁₀H₁₈BrNO₂
badge Registry Numbers
MDL Number MFCD24382790
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the construction of complex organic structures, especially those containing azetidine rings, which are valuable in drug discovery due to their unique pharmacological properties. The bromoethyl group attached to the azetidine ring allows for further functionalization through nucleophilic substitution reactions, enabling the creation of diverse derivatives. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances the stability of the molecule during synthetic processes and can be selectively removed under mild conditions, making it a versatile building block in medicinal chemistry. Its applications are particularly relevant in the synthesis of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,279.00
inventory 250mg
10-20 days ฿14,112.00
inventory 1g
10-20 days ฿37,125.00
tert-Butyl 3-(2-bromoethyl)azetidine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the construction of complex organic structures, especially those containing azetidine rings, which are valuable in drug discovery due to their unique pharmacological properties. The bromoethyl group attached to the azetidine ring allows for further functionalization through nucleophilic substitution reactions, enabling the creation of diverse derivatives. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances the stability of the molecule during synthetic processes and can be selectively removed under mild conditions, making it a versatile building block in medicinal chemistry. Its applications are particularly relevant in the synthesis of compounds targeting central nervous system disorders, inflammation, and other therapeutic areas.
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