5-Methyl-1H-indole-3-carboxylic acid

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Reagent Code: #206850
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CAS Number 10242-02-1

science Other reagents with same CAS 10242-02-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.18 g/mol
Formula C₁₀H₉NO₂
thermostat Physical Properties
Boiling Point 421.2°C
inventory_2 Storage & Handling
Storage 2-8°C

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. It serves as a building block for indole-based compounds with potential biological activity, including anti-inflammatory, antiviral, and anticancer properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to mimic natural indole alkaloid structures. Also utilized in the preparation of fluorescent probes and dyes for biochemical imaging applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,250.00
inventory 5g
10-20 days ฿5,840.00
inventory 25g
10-20 days ฿25,360.00

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5-Methyl-1H-indole-3-carboxylic acid
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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. It serves as a building block for indole-based compounds with potential biological activity, including anti-inflammatory, antiviral, and anticancer properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to mimic natural indole alkaloid structures. Also utilized in the preparati

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor modulators and other central nervous system agents. It serves as a building block for indole-based compounds with potential biological activity, including anti-inflammatory, antiviral, and anticancer properties. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to mimic natural indole alkaloid structures. Also utilized in the preparation of fluorescent probes and dyes for biochemical imaging applications.

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