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2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione is a chemical compound characterized by its molecular formula C13H12O4S. It is a derivative of cyclohexa-2,5-diene-1,4-dione, a type of cyclic enone, featuring two methoxy (CH3O-) groups and a phenylsulfanyl (C6H5S-) group attached to the cyclohexadienedione ring. This unique chemical structure and reactivity may endow it with potential applications in various fields such as organic synthesis, pharmaceuticals, and material science.

69241-94-7

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69241-94-7 Usage

Uses

Used in Organic Synthesis:
2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione is used as a potential pharmaceutical agent due to its unique chemical properties. Its reactivity and structural features may contribute to the development of new drugs with novel therapeutic effects. Further research is required to explore its potential as a pharmaceutical compound.
Used in Material Science:
2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione is used in material science for the development of new materials with specific properties. Its unique structure and reactivity may enable the creation of materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials with specific mechanical, electrical, or optical properties.
Further research is needed to fully explore the potential applications and properties of 2,3-dimethoxy-5-(phenylsulfanyl)cyclohexa-2,5-diene-1,4-dione, as its current understanding is limited.

Check Digit Verification of cas no

The CAS Registry Mumber 69241-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,4 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69241-94:
(7*6)+(6*9)+(5*2)+(4*4)+(3*1)+(2*9)+(1*4)=147
147 % 10 = 7
So 69241-94-7 is a valid CAS Registry Number.

69241-94-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethoxy-5-phenylsulfanylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 5-phenylthio-2,3-dimethoxy-1,4-benzoquinone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69241-94-7 SDS

69241-94-7Downstream Products

69241-94-7Relevant academic research and scientific papers

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

Mori, Koichi,Ushio, Tomoe,Okamoto, Tadashi,Kishi, Takeo,Sayo, Hiroteru

, p. 293 - 296 (2007/10/03)

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.

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