5435-36-9

Basic information

• Product Name: 7-METHYLINDOLE-3-ACETIC ACID
• Synonyms: 7-METHYLINDOLE-3-ACETIC ACID;7-METHYLINDOLE-3-ACETIC ACID 98% (HPLC);7-Me-IAA;7-METHYLINDOLE-3-ACETIC ACID(7MeIAA);2-(7-methyl-1H-indol-3-yl)acetic acid;2-(7-methyl-1H-indol-3-yl)ethanoic acid;1H-Indole-3-acetic acid, 7-Methyl-
• CAS NO: 5435-36-9
• Molecular Formula: C11H11NO2
• Molecular Weight: 189.21
• Product Categories: Indoles and derivatives
• Mol File: 5435-36-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 413.8°Cat760mmHg
• Flash Point: 204°C
• Appearance: /
• Density: 1.299g/cm³
• Vapor Pressure: 1.38E-07mmHg at 25°C
• Refractive Index: 1.671
• Storage Temp.: 2-8°C
• Solubility: DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 7-METHYLINDOLE-3-ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 7-METHYLINDOLE-3-ACETIC ACID(5435-36-9)
• EPA Substance Registry System: 7-METHYLINDOLE-3-ACETIC ACID(5435-36-9)

Safety Data

• Hazardous Substances Data: 5435-36-9(Hazardous Substances Data)

Usage

Uses

7-Methylindole-3-acetic Acid is a useful reagent for the preparation of indole-acetamide derivatives for treating mitochondrial dysfunction.

InChI:InChI=1/C11H11NO2/c1-7-3-2-4-9-8(5-10(13)14)6-12-11(7)9/h2-4,6,12H,5H2,1H3,(H,13,14)

Relevant articles and documents

A substituted indole -3 - acetic acid synthesis method (by machine translation)

The present invention provides a substituted indole - 3 - acetic acid synthesis method, comprises the following steps: (1) in order to replace the indole as the starting material, with the acylation reagent under the action of catalyst through the tutor - acylation to obtain the 1, 3 - diacetyl substituted indole; (2) intermediate 1, 3 - diacetyl substituted indole does not need refining, directly with the morpholine and sulfur by the Willgerodt - Kindler rearrangement reaction, the inorganic under the catalysis of alkali hydrolysis, acidified to obtain substituted indole - 3 - acetic acid. (by machine translation)