3-(2-Bromo-1-hydroxyethyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one

97%

Reagent Code: #117393
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CAS Number 1378391-38-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.24 g/mol
Formula C₁₉H₁₇BrO₃
badge Registry Numbers
MDL Number MFCD30536258
thermostat Physical Properties
Boiling Point 580.6±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry for the development of novel therapeutic agents. Its unique structure makes it a valuable intermediate in the synthesis of compounds targeting neurological disorders, particularly those related to serotonin and dopamine pathways. Researchers are exploring its potential in creating drugs for conditions such as depression, anxiety, and neurodegenerative diseases like Parkinson's. Additionally, its bromo and hydroxy functional groups allow for further chemical modifications, enabling the creation of diverse derivatives with enhanced pharmacological properties. Its application in organic synthesis also extends to the study of chromene-based compounds, which are known for their biological activities, including anti-inflammatory and anticancer effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days $57.54
inventory 1g
10-20 days $155.01
inventory 100mg
10-20 days $32.21
3-(2-Bromo-1-hydroxyethyl)-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one
This chemical is primarily utilized in the field of medicinal chemistry for the development of novel therapeutic agents. Its unique structure makes it a valuable intermediate in the synthesis of compounds targeting neurological disorders, particularly those related to serotonin and dopamine pathways. Researchers are exploring its potential in creating drugs for conditions such as depression, anxiety, and neurodegenerative diseases like Parkinson's. Additionally, its bromo and hydroxy functional groups allow for further chemical modifications, enabling the creation of diverse derivatives with enhanced pharmacological properties. Its application in organic synthesis also extends to the study of chromene-based compounds, which are known for their biological activities, including anti-inflammatory and anticancer effects.
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