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Catalog Number:
21905
CAS Number:
84-58-2
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone
Purity:
≥ 98% (Assay)
Synonym(s):
4,5-Dichloro-3,6-dioxo-1,4-cyclohexadiene-1,2-carbonitrile, DDQ
Hazmat
Documents
$47.80 /25G
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Product Information

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone is a versatile compound known for its unique properties and applications in various fields. This chemical is recognized for its strong electron-accepting capabilities, making it an essential reagent in organic synthesis and materials science. It serves as a powerful oxidizing agent and is frequently utilized in the synthesis of dyes, pigments, and pharmaceuticals. Researchers appreciate its role in facilitating complex chemical reactions, particularly in the development of advanced materials and organic electronics.

In addition to its synthetic applications, 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone is also employed in electrochemical studies and as a precursor in the production of conductive polymers. Its stability and reactivity make it a valuable tool for scientists looking to innovate in fields such as nanotechnology and environmental chemistry. With its ability to enhance reaction efficiency and yield, this compound stands out as a preferred choice for professionals seeking reliable and effective solutions in their research and industrial applications.

Synonyms
4,5-Dichloro-3,6-dioxo-1,4-cyclohexadiene-1,2-carbonitrile, DDQ
CAS Number
84-58-2
Purity
≥ 98% (Assay)
Molecular Formula
C8Cl2N2O2
Molecular Weight
227.01
MDL Number
MFCD00001593
PubChem ID
6775
Melting Point
214 - 218 ºC (Lit.)
Appearance
Yellow to orange yellow crystalline powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
4,5-Dichloro-3,6-dioxo-1,4-cyclohexadiene-1,2-carbonitrile, DDQ
CAS Number
84-58-2
Purity
≥ 98% (Assay)
Molecular Formula
C8Cl2N2O2
Molecular Weight
227.01
MDL Number
MFCD00001593
PubChem ID
6775
Melting Point
214 - 218 ºC (Lit.)
Appearance
Yellow to orange yellow crystalline powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
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