Benzyl (3-methylazetidin-3-yl)carbamate hydrochloride

≥95%

Reagent Code: #87077
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CAS Number 1951441-46-5

science Other reagents with same CAS 1951441-46-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.73 g/mol
Formula C₁₂H₁₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD27997413
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. It serves as a key intermediate in the creation of biologically active molecules, especially those targeting neurological disorders and pain management. Its structural features, including the azetidine ring, make it valuable for designing compounds with enhanced binding affinity to specific receptors. Additionally, it is explored in the development of enzyme inhibitors and modulators for therapeutic applications. Its hydrochloride form ensures improved stability and solubility, facilitating its use in various experimental and formulation processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,980.00
inventory 1g
10-20 days ฿5,328.00
inventory 5g
10-20 days ฿18,621.00

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Benzyl (3-methylazetidin-3-yl)carbamate hydrochloride
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. It serves as a key intermediate in the creation of biologically active molecules, especially those targeting neurological disorders and pain management. Its structural features, including the azetidine ring, make it valuable for designing compounds with enhanced binding affinity to specific receptors. Additionally, it is explored in the development of enzyme inhibitors a

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. It serves as a key intermediate in the creation of biologically active molecules, especially those targeting neurological disorders and pain management. Its structural features, including the azetidine ring, make it valuable for designing compounds with enhanced binding affinity to specific receptors. Additionally, it is explored in the development of enzyme inhibitors and modulators for therapeutic applications. Its hydrochloride form ensures improved stability and solubility, facilitating its use in various experimental and formulation processes.

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