2-(7-Chloro-1H-indol-3-yl)acetic acid

95%

Reagent Code: #41808
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CAS Number 1912-41-0

science Other reagents with same CAS 1912-41-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.6290 g/mol
Formula C₁₀H₈ClNO₂
badge Registry Numbers
MDL Number MFCD09751728
thermostat Physical Properties
Boiling Point 445.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.483g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its indole structure makes it a valuable building block for developing compounds that interact with serotonin receptors, which are crucial in regulating mood, anxiety, and other cognitive functions. Additionally, it is explored for its potential in creating anti-inflammatory and analgesic agents due to its ability to modulate specific biochemical pathways. Researchers also investigate its derivatives for their anticancer properties, focusing on their ability to inhibit tumor growth or induce apoptosis in cancer cells.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,115.00

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2-(7-Chloro-1H-indol-3-yl)acetic acid
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its indole structure makes it a valuable building block for developing compounds that interact with serotonin receptors, which are crucial in regulating mood, anxiety, and other cognitive functions. Additionally, it is explored for its potential in creating anti-inflammatory and analgesic agents due to its ability to modulate specific biochemical pathways. Researchers also investigate its derivatives for their anticancer properties, focusing on their ability to inhibit tumor growth or induce apoptosis in cancer cells.
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