79236-82-1 Usage
Uses
Used in Organic Synthesis:
2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions. Its unique structure allows it to act as an intermediate or a building block in the synthesis of more complex molecules.
Used in Rubber and Plastic Industry:
In the rubber and plastic industry, 2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole is used as a crosslinking agent. It helps to improve the mechanical properties and durability of rubber and plastic materials by forming covalent bonds between polymer chains, resulting in a stronger and more stable material.
Used in Pharmaceutical Industry:
2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole is used in the pharmaceutical industry for its potential applications in drug development. Its chemical properties make it a candidate for the synthesis of new drugs or as a component in existing medications.
Safety Precautions:
It is important to handle 2,5-bis[(2,4-dinitrophenyl)sulfanyl]-1,3,4-thiadiazole with caution as it is toxic and may cause skin and eye irritation. Proper safety measures, such as wearing protective clothing and using appropriate containment, should be taken to minimize exposure and potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 79236-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,3 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79236-82:
(7*7)+(6*9)+(5*2)+(4*3)+(3*6)+(2*8)+(1*2)=161
161 % 10 = 1
So 79236-82-1 is a valid CAS Registry Number.
79236-82-1Relevant academic research and scientific papers
Synthesis of some novel 1,3,4- and 1,2,4-thiadiazole derivatives
Dueruest, Yasar
experimental part, p. 2923 - 2935 (2010/04/28)
Synthesis and spectral characterization of novel 1,3,4-thiadiazole derivatives including one organo-mercury compound are described. Their structure elucidation was performed by means of spectroscopic and physical methods (IR, 1H NMR, 13/s
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.
