69241-94-7

Basic information

• Product Name: 2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione
• Synonyms: 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-(phenylthio)-
• CAS NO: 69241-94-7
• Molecular Formula: C₁₄H₁₂O₄S
• Molecular Weight: 276.3077
• Mol File: 69241-94-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 463.6°C at 760 mmHg
• Flash Point: 238.3°C
• Density: 1.31g/cm³
• Vapor Pressure: 8.98E-09mmHg at 25°C
• Refractive Index: 1.61
• CAS DataBase Reference: 2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione(69241-94-7)
• EPA Substance Registry System: 2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione(69241-94-7)

Safety Data

• Hazardous Substances Data: 69241-94-7(Hazardous Substances Data)

Usage

General Description

2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione is a chemical compound with the molecular formula C13H12O4S. It is a derivative of cyclohexa-2,5-diene-1,4-dione, which is a type of cyclic enone. The compound contains two methoxy (CH3O-) groups and a phenylsulfanyl (C6H5S-) group attached to the cyclohexadienedione ring. 2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione may have potential applications in organic synthesis, pharmaceuticals, and material science due to its unique chemical structure and reactivity. Further research is needed to explore the full potential and properties of 2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione.

Upstream product

• 3117-02-0 2,3-dimethoxy-1,4-benzoquinone 
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Relevant articles and documents

Effect of Arylthiolated 2,3-Dimethoxy-1,4-benzoquinones on Respiratory Activity and Lipid Peroxidation in Bovine Heart Mitochondria

A series of arylthiolated 2,3-dimethoxy-1,4-benzoquinones was synthesized and tested for the effect on the respiratory system and the lipid peroxidation in bovine heart mitochondria (BHM). These quinones showed intense inhibitory activities on the respiratory system in BHM. Their inhibitory activity in the succinate oxidase system was greater than that in the NADH oxidase system. No difference between the difference spectra, with and without these quinones, of the reduced minus oxidized forms of cytochromes (cyt.) suggested that these quinones inhibit at the site after cyt. a+a3 in the respiratory chain. Moreover, these quinones were as efficient as exogenous ubiquinone-10 (UQ-10) for the inhibition of lipid peroxidation. 5- And 5,6-di-arylthio groups on the quinone ring were found to be favorable for inhibition of the respiratory system and lipid peroxidation. Our results suggest that arylthiolated 2,3-dimethoxy-1,4-benzoquinones act as antioxidants by increasing the amount of endogenous reduced UQ-10 in BHM.