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Catalog Number:
21905
CAS Number:
84-58-2
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone
Purity:
≥ 98 % (dosage)
Synonym(s):
4,5-Dichloro-3,6-dioxo-1,4-cyclohexadiène-1,2-carbonitrile, DDQ
Hazmat
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Product Information

Il est utilisé comme oxydant pour la déshydrogénation de l'alcool, du phénol, des cétones stéroïdiennes et dans la synthèse des quinoléines à partir d'imines et d'alcynes ou d'alcènes. C'est un réactif de déprotection pour les thioacétals, les acétals et les cétals.

Synonyms
4,5-Dichloro-3,6-dioxo-1,4-cyclohexadiène-1,2-carbonitrile, DDQ
CAS Number
84-58-2
Purity
≥ 98 % (dosage)
Molecular Formula
C8Cl2N2O2
Molecular Weight
227.01
MDL Number
MFCD00001593
PubChem ID
6775
Melting Point
214 - 218 ºC (lit.)
Appearance
Poudre cristalline jaune à jaune orangé
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
4,5-Dichloro-3,6-dioxo-1,4-cyclohexadiène-1,2-carbonitrile, DDQ
CAS Number
84-58-2
Purity
≥ 98 % (dosage)
Molecular Formula
C8Cl2N2O2
Molecular Weight
227.01
MDL Number
MFCD00001593
PubChem ID
6775
Melting Point
214 - 218 ºC (lit.)
Appearance
Poudre cristalline jaune à jaune orangé
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the synthesis of various complex molecules, which is essential for developing new pharmaceuticals and agrochemicals.
  • Electrochemistry: It is employed in electrochemical applications, particularly in the development of sensors and batteries, due to its ability to undergo reversible redox reactions, enhancing energy storage solutions.
  • Polymer Chemistry: The compound is used in the production of conducting polymers, which are crucial for applications in flexible electronics and advanced materials, offering improved conductivity compared to traditional materials.
  • Biological Research: It acts as a potent reagent in biological studies, particularly in the investigation of enzyme activity and mechanisms, aiding researchers in understanding biochemical pathways.
  • Environmental Science: This chemical is utilized in studies examining pollutant degradation, helping to develop methods for environmental remediation and assessing the impact of contaminants in ecosystems.

Citations