850008-37-6

Basic information

• Product Name: 2-(7-METHOXYINDOL-1H-3-YL)ACETIC ACID
• Synonyms: 7-METHOXYINDOLE-3-ACETIC ACID;2-(7-METHOXYINDOL-1H-3-YL)ACETIC ACID;2-(7-methoxy-1H-indol-3-yl)acetic acid
• CAS NO: 850008-37-6
• Molecular Formula: C₁₁H₁₁NO₃
• Molecular Weight: 205.21
• Product Categories: Indoles and derivatives
• Mol File: 850008-37-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(7-METHOXYINDOL-1H-3-YL)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(7-METHOXYINDOL-1H-3-YL)ACETIC ACID(850008-37-6)
• EPA Substance Registry System: 2-(7-METHOXYINDOL-1H-3-YL)ACETIC ACID(850008-37-6)

Safety Data

• Hazardous Substances Data: 850008-37-6(Hazardous Substances Data)

Usage

Derivative of indole

Heterocyclic aromatic organic compound The compound is based on the indole structure, which is a heterocyclic aromatic organic compound with a distinctive chemical and physical properties.

Indole ring contains a methoxy group

This functional group is attached to the indole ring, which may influence the compound's pharmacological properties and potential applications.

Derivative of 7-methoxyindole and acetic acid

The compound is formed by combining 7-methoxyindole and acetic acid, resulting in a new compound with unique properties.

Used in pharmaceutical research and development

The compound is studied for its potential pharmacological properties, which may lead to the development of new drugs and therapies.

Potential applications in the treatment of various diseases and disorders

The compound may be useful in treating a range of health conditions, although more research and testing are needed to confirm its full range of potential uses.

Further research and testing required

The compound's full potential and applications are not yet fully understood, and additional studies are needed to determine its safety and efficacy in various medical contexts.

Upstream product

• 1067080-51-6 C₁₂H₁₃NO₃ 
• 3189-22-8 7-methoxy-1H-indole 
• 50656-47-8 7-methoxyindole-3-glyoxyl chloride 
• 408354-83-6 (7-Methoxy-1H-indol-3-yl)-oxo-acetic acid methyl ester 
• 858233-08-6 (2-carboxy-7-methoxy-indol-3-yl)-acetic acid 

Downstream Products

• 1067137-41-0 C₂₄H₂₈O₄N₂ 

Relevant articles and documents

Three oxidative metabolites of indole-3-acetic acid from Arabidopsis thaliana

Three metabolites of indole-3-acetic acid (IAA), N-(6-hydroxyindol-3-ylacetyl)-phenylalanine (6-OH-IAA-Phe), N-(6-hydroxyindol-3-ylacetyl)-valine (6-OH-IAA-Val), and 1-O-(2-oxoindol-3-ylacetyl)-β-d-glucopyranose (OxIAA-Glc), were found by a liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS)-based search for oxidative IAA metabolites during the vegetative growth of Arabidopsis. Their structures were confirmed by making a comparison of chromatographic characteristics and mass spectra between naturally occurring compounds and synthetic standards. An incorporation study using deuterium-labeled compounds showed that 6-OH-IAA-Phe and 6-OH-IAA-Val were biosynthesized from IAA-Phe and IAA-Val, respectively, which strongly suggested the formation of these amino acid conjugates of IAA in plants. Both 6-OH-IAA-Phe and 6-OH-IAA-Val were inactive as auxins, as indicated by no significant root growth inhibition in Arabidopsis. Quantitative analysis demonstrated that OxIAA-Glc was present in the largest amount among the metabolites of IAA in Arabidopsis, suggesting that the conversion into OxIAA-Glc represents the main metabolic process regarding IAA in Arabidopsis.