3-(Boc-aminomethyl)azetidine

95%

Reagent Code: #143499
label
Alias Related CAS No.: 1170108-38-9;3-Term-butoxycarbonylaminomethylazetidane
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CAS Number 91188-15-7

science Other reagents with same CAS 91188-15-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.25 g/mol
Formula C₉H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD01861760
thermostat Physical Properties
Boiling Point 285.5±13.0 °C
inventory_2 Storage & Handling
Density 1.0±0.1 g/cm3
Storage 2-8°C, inert gas, light-proof

description Product Description

Used in pharmaceutical synthesis as a building block for drug development, particularly in creating compounds with nitrogen-containing heterocycles. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and CNS-targeted therapeutics. The azetidine ring enhances metabolic stability and solubility in final drug candidates. Suitable for solid-phase and solution-phase peptide-like assembly due to compatibility with various coupling reagents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,470.00
inventory 1g
10-20 days ฿4,910.00
inventory 5g
10-20 days ฿21,080.00

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3-(Boc-aminomethyl)azetidine
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Used in pharmaceutical synthesis as a building block for drug development, particularly in creating compounds with nitrogen-containing heterocycles. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and CNS-targeted therapeutics. The azetidine ring enhances metabolic stability and solubility in final drug candidates. Suitable for solid-phase and solution-phase peptide-like asse

Used in pharmaceutical synthesis as a building block for drug development, particularly in creating compounds with nitrogen-containing heterocycles. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and CNS-targeted therapeutics. The azetidine ring enhances metabolic stability and solubility in final drug candidates. Suitable for solid-phase and solution-phase peptide-like assembly due to compatibility with various coupling reagents.

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