Ethyl 4,7-dichloro-1H-indole-2-carboxylate

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Reagent Code: #183509
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CAS Number 104115-70-0

science Other reagents with same CAS 104115-70-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.10 g/mol
Formula C₁₁H₉Cl₂NO₂
badge Registry Numbers
MDL Number MFCD04966955
thermostat Physical Properties
Boiling Point 402.6±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules, making it valuable in medicinal chemistry for drug discovery. Commonly employed in research settings to prepare analogs for biological evaluation, especially in studies related to neurological disorders and migraine treatments. Also utilized in the preparation of agrochemicals and bioactive compounds due to its reactive functional groups and halogen substitution pattern.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿610.00
inventory 250mg
10-20 days ฿1,220.00
inventory 1g
10-20 days ฿2,460.00
inventory 5g
10-20 days ฿12,240.00

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Ethyl 4,7-dichloro-1H-indole-2-carboxylate
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules, making it valuable in medicinal chemistry for drug discovery. Commonly employed in research settings to prepare analogs for biological evaluation, especially in studies related to neurological disorders and migraine treatments. Also utilized in the prepa

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules, making it valuable in medicinal chemistry for drug discovery. Commonly employed in research settings to prepare analogs for biological evaluation, especially in studies related to neurological disorders and migraine treatments. Also utilized in the preparation of agrochemicals and bioactive compounds due to its reactive functional groups and halogen substitution pattern.

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