Methyl 2,3-dimethyl-1H-indole-5-carboxylate

≥95%

Reagent Code: #209263
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CAS Number 21987-27-9

science Other reagents with same CAS 21987-27-9

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scatter_plot Molecular Information
Weight 203.24 g/mol
Formula C₁₂H₁₃NO₂
badge Registry Numbers
MDL Number MFCD06520938
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its indole core structure makes it valuable in developing drugs targeting neurological and inflammatory conditions. Commonly employed in the preparation of serotonin receptor modulators and kinase inhibitors. Also utilized in research settings for designing novel heterocyclic compounds with potential therapeutic activity. The ester group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿730.00
inventory 250mg
10-20 days ฿1,670.00
inventory 1g
10-20 days ฿6,350.00

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Methyl 2,3-dimethyl-1H-indole-5-carboxylate
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its indole core structure makes it valuable in developing drugs targeting neurological and inflammatory conditions. Commonly employed in the preparation of serotonin receptor modulators and kinase inhibitors. Also utilized in research settings for designing novel heterocyclic compounds with potential therapeutic activity. The ester group allows for further functionalization, enabling the creation of diverse derivati

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its indole core structure makes it valuable in developing drugs targeting neurological and inflammatory conditions. Commonly employed in the preparation of serotonin receptor modulators and kinase inhibitors. Also utilized in research settings for designing novel heterocyclic compounds with potential therapeutic activity. The ester group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies.

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