6-Bromo-5-fluoro-2,3-dihydro-1H-inden-1-one

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Reagent Code: #145301
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CAS Number 1273595-81-5

science Other reagents with same CAS 1273595-81-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.05 g/mol
Formula C₉H₆BrFO
thermostat Physical Properties
Boiling Point 301.4±42.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its structure allows for selective modifications, making it valuable in creating analogs for neuroactive drugs. Commonly employed in research settings to build indanone-based scaffolds with potential anticonvulsant, antidepressant, or anti-inflammatory activity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive sites for cross-coupling and nucleophilic substitution reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,480.00
inventory 1g
10-20 days ฿5,380.00

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6-Bromo-5-fluoro-2,3-dihydro-1H-inden-1-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its structure allows for selective modifications, making it valuable in creating analogs for neuroactive drugs. Commonly employed in research settings to build indanone-based scaffolds with potential anticonvulsant, antidepressant, or anti-inflammatory activity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the pre

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its structure allows for selective modifications, making it valuable in creating analogs for neuroactive drugs. Commonly employed in research settings to build indanone-based scaffolds with potential anticonvulsant, antidepressant, or anti-inflammatory activity. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive sites for cross-coupling and nucleophilic substitution reactions.

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