2-(2-(Dimethylamino)ethyl)-2,3-dihydro-1H-inden-1-one

95%

Reagent Code: #82316
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CAS Number 3409-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.28 g/mol
Formula C₁₃H₁₇NO
badge Registry Numbers
MDL Number MFCD19302158
thermostat Physical Properties
Boiling Point 302.3±11.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.054±0.06 g/cm3(Predicted)
Storage -20°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring both an indanone core and a dimethylaminoethyl group, makes it a versatile building block for developing compounds with potential central nervous system (CNS) activity. Researchers often explore its use in creating ligands for receptors involved in neurological disorders, such as depression, anxiety, and Alzheimer's disease. Additionally, its structural features are valuable in designing molecules with potential anti-inflammatory or analgesic properties. The compound's reactivity and functional groups allow for further chemical modifications, enabling the development of novel therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,550.00
inventory 250mg
10-20 days ฿32,760.00
2-(2-(Dimethylamino)ethyl)-2,3-dihydro-1H-inden-1-one
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring both an indanone core and a dimethylaminoethyl group, makes it a versatile building block for developing compounds with potential central nervous system (CNS) activity. Researchers often explore its use in creating ligands for receptors involved in neurological disorders, such as depression, anxiety, and Alzheimer's disease. Additionally, its structural features are valuable in designing molecules with potential anti-inflammatory or analgesic properties. The compound's reactivity and functional groups allow for further chemical modifications, enabling the development of novel therapeutic agents.
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