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2,3-dimethoxy-5-(naphthalen-2-ylsulfanyl)cyclohexa-2,5-diene-1,4-dione is a synthetic chemical compound characterized by a cyclohexadienedione ring system with methoxy and naphthalen-2-ylsulfanyl substituents. The incorporation of methoxy groups (–OCH3) and a naphthalene ring endows the molecule with notable chemical and biological properties. 2,3-dimethoxy-5-(naphthalen-2-ylsulfanyl)cyclohexa-2,5-diene-1,4-dione exhibits potential biological activities such as antioxidant, anti-inflammatory, and anticancer properties, making it a significant intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structural properties also render it a valuable asset for medicinal chemistry and drug discovery research.

58511-94-7

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58511-94-7 Usage

Uses

Used in Pharmaceutical Industry:
2,3-dimethoxy-5-(naphthalen-2-ylsulfanyl)cyclohexa-2,5-diene-1,4-dione is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activities, including antioxidant, anti-inflammatory, and anticancer properties. Its unique structure and reactivity contribute to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-dimethoxy-5-(naphthalen-2-ylsulfanyl)cyclohexa-2,5-diene-1,4-dione serves as a key intermediate in the production of agrochemicals, leveraging its chemical properties to enhance crop protection and yield.
Used in Medicinal Chemistry Research:
2,3-dimethoxy-5-(naphthalen-2-ylsulfanyl)cyclohexa-2,5-diene-1,4-dione is utilized as a valuable tool in medicinal chemistry research, where its unique structural properties aid in the exploration of new drug candidates and the understanding of molecular interactions.
Used in Drug Discovery:
2,3-dimethoxy-5-(naphthalen-2-ylsulfanyl)cyclohexa-2,5-diene-1,4-dione is employed in drug discovery efforts, capitalizing on its potential biological activities to identify and develop new therapeutic agents with improved efficacy and selectivity in treating various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 58511-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,1 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58511-94:
(7*5)+(6*8)+(5*5)+(4*1)+(3*1)+(2*9)+(1*4)=137
137 % 10 = 7
So 58511-94-7 is a valid CAS Registry Number.

58511-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:58511-94-7 SDS

58511-94-7Downstream Products

58511-94-7Relevant 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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