Ethyl 3-chloro-1H-indole-2-carboxylate

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Reagent Code: #185267
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CAS Number 38343-91-8

science Other reagents with same CAS 38343-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.66 g/mol
Formula C₁₁H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD11106782
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in the preparation of indole-based bioactive compounds due to its reactive chloro and ester functional groups. Also utilized in research settings for the construction of complex heterocyclic systems through nucleophilic substitution or cross-coupling reactions. Its structural features make it valuable in medicinal chemistry for designing analogs with potential anti-inflammatory, antiviral, or anticancer activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,540.00
inventory 1g
10-20 days ฿13,170.00
inventory 250mg
10-20 days ฿3,790.00

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Ethyl 3-chloro-1H-indole-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in the preparation of indole-based bioactive compounds due to its reactive chloro and ester functional groups. Also utilized in research settings for the construction of complex heterocyclic systems through nucleophilic substitution or cross-coupling reactions. Its structural features make it valuable in medicinal chemi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. Commonly employed in the preparation of indole-based bioactive compounds due to its reactive chloro and ester functional groups. Also utilized in research settings for the construction of complex heterocyclic systems through nucleophilic substitution or cross-coupling reactions. Its structural features make it valuable in medicinal chemistry for designing analogs with potential anti-inflammatory, antiviral, or anticancer activity.

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