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Catalog Number:
21905
CAS Number:
84-58-2
2,3-Dicloro-5,6-diciano-1,4-benzoquinona
Purity:
≥ 98% (ensayo)
Synonym(s):
4,5-Dicloro-3,6-dioxo-1,4-ciclohexadieno-1,2-carbonitrilo, DDQ
Hazmat
Documents
$47.80 /25G
Tamaño
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Product Information

Se utiliza como oxidante para la deshidrogenación de alcoholes, fenoles, cetonas esteroidales y en la síntesis de quinolinas a partir de iminas y alquinos o alquenos. Es un reactivo de desprotección de tioacetales, acetales y cetales.

Synonyms
4,5-Dicloro-3,6-dioxo-1,4-ciclohexadieno-1,2-carbonitrilo, DDQ
CAS Number
84-58-2
Purity
≥ 98% (ensayo)
Molecular Formula
C8Cl2N2O2
Molecular Weight
227.01
MDL Number
MFCD00001593
PubChem ID
6775
Melting Point
214 - 218 ºC (Lit.)
Appearance
Polvo cristalino de color amarillo a amarillo anaranjado.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
4,5-Dicloro-3,6-dioxo-1,4-ciclohexadieno-1,2-carbonitrilo, DDQ
CAS Number
84-58-2
Purity
≥ 98% (ensayo)
Molecular Formula
C8Cl2N2O2
Molecular Weight
227.01
MDL Number
MFCD00001593
PubChem ID
6775
Melting Point
214 - 218 ºC (Lit.)
Appearance
Polvo cristalino de color amarillo a amarillo anaranjado.
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
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.

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