7653-69-2 Usage
General Description
3-oxo-1,5-petanedithioylbis(2-thiazole) is a chemical compound consisting of a six-membered ring containing two sulfur atoms and two carbon atoms, with a ketone group and two thiazole rings attached to it. It is used as a building block in the synthesis of various organic compounds and pharmaceuticals. 3-oxo-1,5-petanedithioylbis(2-thiazole) has potential applications in the development of drugs for the treatment of various diseases, as well as in the production of specialty chemicals and materials. Its unique structure and reactivity make it a valuable intermediate in organic synthesis, with potential for further investigation and development in various fields of chemistry and related 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.
