Ethyl 5,7-dichloro-1H-indole-2-carboxylate

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Reagent Code: #183507
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CAS Number 4792-70-5

science Other reagents with same CAS 4792-70-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.10 g/mol
Formula C₁₁H₉Cl₂NO₂
badge Registry Numbers
MDL Number MFCD03084730
thermostat Physical Properties
Boiling Point 405°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used primarily as a key intermediate in the synthesis of indomethacin, a nonsteroidal anti-inflammatory drug (NSAID). Its structure allows for selective halogenation and ester functionality, making it valuable in pharmaceutical research for developing analogs with improved potency and reduced side effects. Also employed in the preparation of other indole-based bioactive compounds targeting pain, inflammation, and certain cancers. Its stability and reactivity profile support use in multi-step organic syntheses, particularly in medicinal chemistry workflows.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿450.00
inventory 1g
10-20 days ฿1,350.00

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Ethyl 5,7-dichloro-1H-indole-2-carboxylate
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Used primarily as a key intermediate in the synthesis of indomethacin, a nonsteroidal anti-inflammatory drug (NSAID). Its structure allows for selective halogenation and ester functionality, making it valuable in pharmaceutical research for developing analogs with improved potency and reduced side effects. Also employed in the preparation of other indole-based bioactive compounds targeting pain, inflammation, and certain cancers. Its stability and reactivity profile support use in multi-step organic synt

Used primarily as a key intermediate in the synthesis of indomethacin, a nonsteroidal anti-inflammatory drug (NSAID). Its structure allows for selective halogenation and ester functionality, making it valuable in pharmaceutical research for developing analogs with improved potency and reduced side effects. Also employed in the preparation of other indole-based bioactive compounds targeting pain, inflammation, and certain cancers. Its stability and reactivity profile support use in multi-step organic syntheses, particularly in medicinal chemistry workflows.

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