72798-32-4

Basic information

• Product Name: 6,8-DICHLORO-3-CYANOCHROMONE
• Synonyms: 6,8-DICHLORO-3-CYANOCHROMONE;6,8-DICHLORO-4-OXO-4 H-1-BENZOPYRAN-3-CARBONITRILE;6,8-DICHLORO-4-OXO-4H-CHROMENE-3-CARBONITRILE;3-CYANO-6,8-DICHLOROCHROMONE;6,8-DICHLORO-3-CYANOCHROMONE 97%;6,8-Dichlorochromone-3-carbonitrile
• CAS NO: 72798-32-4
• Molecular Formula: C₁₀H₃Cl₂NO₂
• Molecular Weight: 240.04
• Product Categories: Chromones
• Mol File: 72798-32-4.mol
• Article Data: 1

Chemical Properties

• Melting Point: 169-174 °C(lit.)
• Boiling Point: 425.9ºC at 760 mmHg
• Flash Point: 211.4ºC
• Appearance: /
• Density: 1.6g/cm3
• Vapor Pressure: 1.85E-07mmHg at 25°C
• Refractive Index: 1.649
• CAS DataBase Reference: 6,8-DICHLORO-3-CYANOCHROMONE(CAS DataBase Reference)
• NIST Chemistry Reference: 6,8-DICHLORO-3-CYANOCHROMONE(72798-32-4)
• EPA Substance Registry System: 6,8-DICHLORO-3-CYANOCHROMONE(72798-32-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 72798-32-4(Hazardous Substances Data)

Usage

General Description

6,8-Dichloro-3-cyanochromone is a chemical compound with the molecular formula C10H3Cl2NO2. It is a chromone derivative that contains two chlorine atoms and a cyano group. 6,8-DICHLORO-3-CYANOCHROMONE is known for its potential use in pharmaceutical and medicinal applications due to its bioactive properties. It has been studied for its potential as an anti-inflammatory and anti-tumor agent. Additionally, 6,8-dichloro-3-cyanochromone has also been investigated for its antioxidant and antiviral activities. Its unique molecular structure and properties make it a promising candidate for further research and development in the field of medicinal chemistry.

InChI:InChI=1/C10H3Cl2NO2/c11-7-2-5-1-6(4-13)10(14)15-9(5)8(12)3-7/h1-3H

Downstream Products

• 1338367-50-2 dimethyl 5,7-dichloro-5'-cyano-4'-(cyclohexylamino)-3-oxo-3H-spiro[benzofuran-2,1'-cyclopenta[2,4]diene]-2',3'-dicarboxylate 

Relevant articles and documents

A rare acid-promoted elimination of O-methyl oximes: A practical synthesis of 3-cyano-4-benzopyrones

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