58069-93-5 Usage
Uses
Used in Marine Biology Research:
DiMethyl-d6 Trisulfide is used as a research compound for studying the pathways and substrate specificity of DMSP (Dimethylsulfoniopropionate) catabolism in marine bacteria of the Roseobacter clade. This application is crucial for understanding the role of these bacteria in the marine ecosystem and their contribution to the biogeochemical cycling of sulfur and carbon.
Used in Chemical Analysis:
Due to its stable isotope labeling, DiMethyl-d6 Trisulfide can be employed as an internal standard or a reference compound in various analytical techniques, such as gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS). This helps in the accurate quantification and identification of target compounds in complex samples, including environmental, biological, and industrial samples.
Used in Pharmaceutical Industry:
DiMethyl-d6 Trisulfide can be utilized as a building block or a synthetic intermediate in the development of novel pharmaceutical compounds. Its unique chemical properties and stable isotope labeling make it a valuable tool for drug discovery and optimization processes.
Used in Environmental Science:
In environmental science, DiMethyl-d6 Trisulfide can be employed as a tracer compound to study the fate and transport of pollutants in the environment. Its stable isotope labeling allows for the differentiation between naturally occurring and anthropogenic sources of pollutants, providing valuable insights into the environmental impact of human activities.
Check Digit Verification of cas no
The CAS Registry Mumber 58069-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58069-93:
(7*5)+(6*8)+(5*0)+(4*6)+(3*9)+(2*9)+(1*3)=155
155 % 10 = 5
So 58069-93-5 is a valid CAS Registry Number.
58069-93-5Relevant academic research and scientific papers
K2S as Sulfur Source and DMSO as Carbon Source for the Synthesis of 2-Unsubstituted Benzothiazoles
Deng, Guobo,Kuang, Daizhi,Liang, Yun,Yang, Yuan,Yu, Jiangxi,Zhang, Fuxing,Zhu, Xiaoming
supporting information, p. 3789 - 3793 (2020/06/04)
We describe a three-component reaction of o-iodoanilines with K2S and DMSO that provides 2-unsubstituted benzothiazoles in moderate to good isolated yields with good functional group tolerance. Electron-rich aromatic amines and o-phenylenediamines instead of o-iodoanilines provided 2-unsubstituted benzothiazoles and 2-unsubstituted benzimidazoles with and without K2S under similar conditions. Notably, DMSO plays three vital roles: carbon source, solvent, and oxidant.
