4-Chloro-1H-inden-2(3H)-one

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Reagent Code: #160168
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CAS Number 74124-90-6

science Other reagents with same CAS 74124-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.6 g/mol
Formula C₉H₇ClO
badge Registry Numbers
MDL Number MFCD09744094
thermostat Physical Properties
Boiling Point 294°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of steroidal and non-steroidal anti-inflammatory agents. It serves as a building block in organic synthesis due to its reactive carbonyl and aromatic functionalities, enabling derivatization for drug discovery. Also employed in the preparation of indene-based compounds with potential biological activity, including kinase inhibitors and hormone modulators. Its chloro-substituted structure allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,810.00
inventory 250mg
10-20 days ฿6,130.00
inventory 1g
10-20 days ฿14,680.00
inventory 100mg
10-20 days ฿4,360.00
inventory 5g
10-20 days ฿58,620.00

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4-Chloro-1H-inden-2(3H)-one
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of steroidal and non-steroidal anti-inflammatory agents. It serves as a building block in organic synthesis due to its reactive carbonyl and aromatic functionalities, enabling derivatization for drug discovery. Also employed in the preparation of indene-based compounds with potential biological activity, including kinase inhibitors and hormone modulators. Its chloro-substituted structure allows for further fun

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of steroidal and non-steroidal anti-inflammatory agents. It serves as a building block in organic synthesis due to its reactive carbonyl and aromatic functionalities, enabling derivatization for drug discovery. Also employed in the preparation of indene-based compounds with potential biological activity, including kinase inhibitors and hormone modulators. Its chloro-substituted structure allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry research.

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