Ethyl 5-chloro-1-methyl-1H-indole-2-carboxylate

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Reagent Code: #180659
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CAS Number 59908-53-1

science Other reagents with same CAS 59908-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.68 g/mol
Formula C₁₂H₁₂ClNO₂
badge Registry Numbers
MDL Number MFCD08679183
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a synthetic intermediate in organic chemistry, especially in the development of pharmaceuticals and bioactive compounds. Its structure supports derivatization for research into central nervous system agents and receptor modulators. Commonly employed in the synthesis of indole-based analogs for medicinal chemistry screening. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies due to the reactive sites on the indole core and ester functionality.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,040.00
inventory 1g
10-20 days ฿24,400.00
inventory 5g
10-20 days ฿85,380.00

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Ethyl 5-chloro-1-methyl-1H-indole-2-carboxylate
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Used primarily as a synthetic intermediate in organic chemistry, especially in the development of pharmaceuticals and bioactive compounds. Its structure supports derivatization for research into central nervous system agents and receptor modulators. Commonly employed in the synthesis of indole-based analogs for medicinal chemistry screening. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies due to the reactive sites on the indole core and ester functionality.

Used primarily as a synthetic intermediate in organic chemistry, especially in the development of pharmaceuticals and bioactive compounds. Its structure supports derivatization for research into central nervous system agents and receptor modulators. Commonly employed in the synthesis of indole-based analogs for medicinal chemistry screening. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies due to the reactive sites on the indole core and ester functionality.

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