7653-69-2 Usage
Description
3-oxo-1,5-petanedithioylbis(2-thiazole) is a chemical compound characterized by a six-membered ring with two sulfur atoms and two carbon atoms, featuring a ketone group and two thiazole rings. This unique structure endows it with distinctive reactivity and potential as a valuable intermediate in organic synthesis.
Uses
Used in Pharmaceutical Industry:
3-oxo-1,5-petanedithioylbis(2-thiazole) serves as a building block in the synthesis of various pharmaceuticals, contributing to the development of drugs for the treatment of a range of diseases. Its unique structure and reactivity make it a promising candidate for creating novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 3-oxo-1,5-petanedithioylbis(2-thiazole) is utilized as an intermediate, playing a crucial role in the creation of diverse organic compounds. Its potential for further investigation and development in this area highlights its importance in advancing chemical research and applications.
Used in Specialty Chemicals and Materials Production:
3-oxo-1,5-petanedithioylbis(2-thiazole) also finds application in the production of specialty chemicals and materials, where its distinctive properties can be harnessed to create innovative and high-performance products across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 7653-69-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7653-69:
(6*7)+(5*6)+(4*5)+(3*3)+(2*6)+(1*9)=122
122 % 10 = 2
So 7653-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N2S3/c1-7-3-5-6-4(8-2)9-3/h1-2H3
7653-69-2Relevant articles and documents
Synthesis, 1H NMR Spectral Properties and Conformational Preferences of some Open-chain and Cyclic Aromatic Sulphides Containing Pyridine or 1,3,4-Thiadiazole Units
Bottino, Francesco,Pappalardo, Sebastiano
, p. 1 - 6 (2007/10/02)
The conformational preferences in solution of eight new open-chain and cyclic aromatic sulphides containing pyridine or 1,3,4-thiadiazole units have been investigated, parallel to those of some structurally related phenyl sulphides, by means of 1H NMR spectroscopy.The results obtained have shown that replacement of phenyl by the pyridyl or the 1,3,4-thiadiazolyl moieties induces slightly different propeller arrangements, ascribed to the higher conjugative tendency of both electron-deficient heteroaromatic rings, in all open-chain mixed sulphides, in opposition to the skew arrangements observed for phenyl sulphide derivatives.No prominent differences have been found for cyclic sulphides, which preferentially adopt the sterically unhindered saddle shape conformation.
