4-Methyl-1H-indole-2-carboxylic acid methyl ester

98%

Reagent Code: #207571
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CAS Number 136831-13-5

science Other reagents with same CAS 136831-13-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.22 g/mol
Formula C₁₁H₁₁NO₂
badge Registry Numbers
MDL Number MFCD04966966
inventory_2 Storage & Handling
Storage Room temperature, dry

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 research settings for the preparation of indole-based compounds with potential biological activity. Its ester functionality allows for further chemical modifications, making it valuable in medicinal chemistry for building complex molecular structures. Also utilized in the creation of analogs for structure-activity relationship studies. Additionally, it serves as a starting material for producing fluorescent or luminescent compounds used in biological research and analytical chemistry, due to its modifiable structure that enables special fluorescence or target-binding properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿520.00
inventory 1g
10-20 days ฿4,130.00

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4-Methyl-1H-indole-2-carboxylic acid methyl ester
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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 research settings for the preparation of indole-based compounds with potential biological activity. Its ester functionality allows for further chemical modifications, making it valuable in medicinal chemistry for building complex molecular structures. Also utilized in the creation of analogs for structure-activity re

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 research settings for the preparation of indole-based compounds with potential biological activity. Its ester functionality allows for further chemical modifications, making it valuable in medicinal chemistry for building complex molecular structures. Also utilized in the creation of analogs for structure-activity relationship studies. Additionally, it serves as a starting material for producing fluorescent or luminescent compounds used in biological research and analytical chemistry, due to its modifiable structure that enables special fluorescence or target-binding properties.

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