5-Methoxyindole-2-carboxylic acid
97%
Reagent
Code: #120291
Alias
NSC 30927;5-Methoxyindole-2-carboxylic acid
CAS Number
4382-54-1
blur_circular Chemical Specifications
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Molecular Information
Weight
191.18 g/mol
Formula
C₁₀H₉NO₃
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Registry Numbers
EC Number
224-487-6
MDL Number
MFCD00005614
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Physical Properties
Melting Point
199-201 °C(lit.)
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Storage & Handling
Storage
2~8°C
description Product Description
5-Methoxyindole-2-carboxylic acid is primarily utilized in the field of organic synthesis as a building block for the development of more complex chemical compounds. Its structure makes it a valuable intermediate in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic effects. Researchers often use it to develop molecules that interact with biological systems, such as enzyme inhibitors or receptor modulators. Additionally, it finds application in the study of indole derivatives, which are known for their diverse biological activities. Its methoxy and carboxylic acid functional groups provide reactive sites for further chemical modifications, enabling the creation of novel compounds for drug discovery and development.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (HPLC) | 97-100 |
Purity (Neutralization Titration) | 96.5-103.5 |
Appearance | White to grey to light brown powder |
Infrared Spectrum | Conforms To Structure |
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5-Methoxyindole-2-carboxylic acid
5-Methoxyindole-2-carboxylic acid is primarily utilized in the field of organic synthesis as a building block for the development of more complex chemical compounds. Its structure makes it a valuable intermediate in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic effects. Researchers often use it to develop molecules that interact with biological systems, such as enzyme inhibitors or receptor modulators. Additionally, it finds application in the study of indole derivatives, which are known for their diverse biological activities. Its methoxy and carboxylic acid functional groups provide reactive sites for further chemical modifications, enabling the creation of novel compounds for drug discovery and development.
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