Methyl 4-chloro-1H-indole-6-carboxylate

95%

Reagent Code: #208946
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CAS Number 885522-78-1

science Other reagents with same CAS 885522-78-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.63 g/mol
Formula C₁₀H₈ClNO₂
badge Registry Numbers
MDL Number MFCD07781543
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive indole derivatives. It serves as a building block for developing serotonin receptor modulators and other neuroactive compounds. Commonly employed in the preparation of analogs for drug discovery programs targeting central nervous system disorders. Also utilized in the development of anti-inflammatory and anticancer agents due to the indole scaffold’s prevalence in medicinal chemistry. Its ester functionality allows for easy modification, making it valuable in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿368.50
inventory 250mg
10-20 days ฿566.50
inventory 1g
10-20 days ฿1,199.00
inventory 5g
10-20 days ฿5,846.50

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Methyl 4-chloro-1H-indole-6-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive indole derivatives. It serves as a building block for developing serotonin receptor modulators and other neuroactive compounds. Commonly employed in the preparation of analogs for drug discovery programs targeting central nervous system disorders. Also utilized in the development of anti-inflammatory and anticancer agents due to the indole scaffold’s prevalence in medicinal chemistry. Its ester functionality allows for ea

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive indole derivatives. It serves as a building block for developing serotonin receptor modulators and other neuroactive compounds. Commonly employed in the preparation of analogs for drug discovery programs targeting central nervous system disorders. Also utilized in the development of anti-inflammatory and anticancer agents due to the indole scaffold’s prevalence in medicinal chemistry. Its ester functionality allows for easy modification, making it valuable in structure-activity relationship studies.

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