26542-77-8 Usage
Uses
Used in Organic Synthesis:
3-CHLORO-5-[2-(3-CHLORO-1,2,4-THIADIAZOL-5-YL)DISULFANYL]-1,2,4-THIADIAZOLE is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its structural features and functional groups facilitate the formation of new chemical bonds and the synthesis of target compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-CHLORO-5-[2-(3-CHLORO-1,2,4-THIADIAZOL-5-YL)DISULFANYL]-1,2,4-THIADIAZOLE is used as a building block for the development of new drugs. Its unique structure and functional groups can be leveraged to design and synthesize pharmaceutical compounds with specific therapeutic properties.
Used in Agrochemicals:
3-CHLORO-5-[2-(3-CHLORO-1,2,4-THIADIAZOL-5-YL)DISULFANYL]-1,2,4-THIADIAZOLE is utilized in the agrochemical sector as a precursor for the synthesis of novel agrochemicals. Its potential to form stable and bioactive compounds makes it a valuable component in the development of pesticides, herbicides, and other agricultural chemicals.
Used in Research and Development:
3-CHLORO-5-[2-(3-CHLORO-1,2,4-THIADIAZOL-5-YL)DISULFANYL]-1,2,4-THIADIAZOLE is employed in research and development settings to explore its chemical properties and interactions. The presence of multiple chlorine atoms and sulfur-containing groups makes it an interesting subject for studies aimed at understanding its reactivity, stability, and potential applications in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 26542-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,4 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26542-77:
(7*2)+(6*6)+(5*5)+(4*4)+(3*2)+(2*7)+(1*7)=118
118 % 10 = 8
So 26542-77-8 is a valid CAS Registry Number.
26542-77-8Relevant academic research and scientific papers
Investigations on organo-sulfur-nitrogen rings and the thiocyanogen polymer, (SCN)x
Russell Bowman,Burchell, Colin J.,Kili, Petr,Slawin, Alexandra M. Z.,Wormald, Philip,Woollins, J. Derek
, p. 6366 - 6381 (2008/09/18)
The synthesis and full characterisation of a series of 1,2,4-thiadiazoles is reported. (SCN)x has been studied by a variety of techniques and the data compared with 1,2,4-thiadiazole and 1,2,4-dithiazoles. The observed data suggest that the polymer consists of 1,2,4-dithiazole rings linked by nitrogen atoms. For (SCN)x, the MALDI-TOF mass spectroscopy showed a parent ion at 1149 and a series of peaks with (SCN)2 repeat units (116 m/z); this result implies that (SCN)2 may be the monomer unit of the polymer. Its IR spectrum shows a very broad peak with maximum at 1134 cm-1 consisting of several overlapping peaks in the same region as ring vibrations for 1,2,4-thiadiazole and 1,2,4-dithiazole compounds. Peaks in the Raman spectrum in the range 400-480 cm-1 support the presence of disulfide units within the polymer. The solid-state 13C NMR (99% 13C-labelled) spectrum is dominated by two singlets of equal intensity at approximately 187 and 184 ppm with low intensity peaks in the range 152-172 ppm, in approximately the same range as both 1,2,4-thiadiazoles and 1,2,4-dithiazoles. The solid-state 15N NMR (99% 15N labelled) spectrum displays two major peaks of similar intensity at 236.9 and 197.2 ppm, which are clearly very different environments to those observed in bis(3-bromo-1,2,4-thiadiazol-5-yl) disulfide, but similar to 1,2,4-dithiazoles. The X-ray structures of seven C-S-N systems are reported. Preliminary studies on (SeCN)x suggest that literature references to this polymer may be in error with the red solid actually being red selenium.
