886362-21-6

Basic information

• Product Name: 4,6-DICHLORO-2-METHYLINDOLE
• Synonyms: 4,6-Dichloro-2-methyl-1H-indole;4,6-Dichloro-2-methylindole;2-Methyl-4,6-dichloro-1H-indole;1H-Indole, 4,6-dichloro-2-methyl-
• CAS NO: 886362-21-6
• Molecular Formula: C9H7Cl2N
• Molecular Weight: 200.06
• Product Categories: Indole;Aromatics;Heterocycles;Indole Derivatives;Intermediates
• Mol File: 886362-21-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 336.7 °C at 760 mmHg
• Flash Point: 187.8 °C
• Appearance: /
• Density: 1.408 g/cm³
• Vapor Pressure: 0.000216mmHg at 25°C
• Refractive Index: 1.671
• Storage Temp.: 2-8°C
• PKA: 15.77±0.30(Predicted)
• CAS DataBase Reference: 4,6-DICHLORO-2-METHYLINDOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-DICHLORO-2-METHYLINDOLE(886362-21-6)
• EPA Substance Registry System: 4,6-DICHLORO-2-METHYLINDOLE(886362-21-6)

Safety Data

• Hazardous Substances Data: 886362-21-6(Hazardous Substances Data)

Usage

Description

4,6-Dichloro-2-methylindole, also known as 4,6-DICHLORO-2-METHYLINDOLE, is a trisubstituted indole compound characterized by the presence of two chlorine atoms at the 4 and 6 positions and a methyl group at the 2 position. This structural feature endows it with unique chemical and biological properties, making it a versatile building block in the synthesis of various biologically active compounds.

Uses

Used in Pharmaceutical Industry:
4,6-DICHLORO-2-METHYLINDOLE is used as a key intermediate in the synthesis of various biologically active compounds, including pharmaceuticals, for its ability to modulate the activity of target proteins and enzymes. Its unique structural features allow for the development of novel drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 4,6-DICHLORO-2-METHYLINDOLE is used as a precursor in the synthesis of bioactive molecules with potential applications as pesticides, herbicides, or insecticides. Its chemical properties enable the development of new agrochemicals with enhanced performance and reduced environmental impact.
Used in Research and Development:
4,6-DICHLORO-2-METHYLINDOLE is also utilized in research and development settings as a valuable tool for studying the structure-activity relationships of indole-containing compounds. Its unique substitution pattern allows researchers to investigate the effects of specific functional groups on the biological activity of indole derivatives, leading to the discovery of new lead compounds and potential therapeutic agents.

InChI:InChI=1/C9H7Cl2N/c1-5-2-7-8(11)3-6(10)4-9(7)12-5/h2-4,12H,1H3