(1-Benzylazetidine-2,4-diyl)dimethanol

95%

Reagent Code: #84997
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CAS Number 127310-66-1

science Other reagents with same CAS 127310-66-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.27 g/mol
Formula C₁₂H₁₇NO₂
badge Registry Numbers
MDL Number MFCD28991841
thermostat Physical Properties
Boiling Point 342.9 °C(Predicted)
inventory_2 Storage & Handling
Density 1.167 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules. Its structure, featuring both azetidine and benzyl groups, makes it a valuable intermediate in the creation of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Additionally, it is employed in the preparation of ligands for metal-catalyzed reactions, enhancing the efficiency of catalytic processes in organic synthesis. Its dual hydroxyl groups allow for further functionalization, making it versatile in the design of complex chemical entities for medicinal chemistry and material science applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,800.00
inventory 100mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿5,400.00

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(1-Benzylazetidine-2,4-diyl)dimethanol
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This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules. Its structure, featuring both azetidine and benzyl groups, makes it a valuable intermediate in the creation of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Additionally, it is employed in the preparation of ligands for metal-catalyzed reactions, enhancing the efficiency of catalytic processes in organic synthesis.

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules. Its structure, featuring both azetidine and benzyl groups, makes it a valuable intermediate in the creation of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Additionally, it is employed in the preparation of ligands for metal-catalyzed reactions, enhancing the efficiency of catalytic processes in organic synthesis. Its dual hydroxyl groups allow for further functionalization, making it versatile in the design of complex chemical entities for medicinal chemistry and material science applications.

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