963-15-5 Usage
Uses
Used in Organic Synthesis:
CIS-1,2-BIS(PHENYLSULFONYL)ETHYLENE is used as a reagent for the formation of carbon-carbon bonds, which is crucial in the synthesis of various organic compounds.
Used in Polymer Production:
In the polymer industry, CIS-1,2-BIS(PHENYLSULFONYL)ETHYLENE is used as a cross-linking agent, enhancing the properties of materials such as plastics and adhesives by improving their structural integrity and durability.
Used in Pharmaceutical Development:
CIS-1,2-BIS(PHENYLSULFONYL)ETHYLENE has been studied for its potential applications in pharmaceuticals, indicating its possible use as a precursor or component in the development of new drugs.
Used in Agrochemical Formulation:
CIS-1,2-BIS(PHENYLSULFONYL)ETHYLENE is also being explored for its potential use in agrochemicals, suggesting that it could be utilized in the development of pesticides or other agricultural chemicals to improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 963-15-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 963-15:
(5*9)+(4*6)+(3*3)+(2*1)+(1*5)=85
85 % 10 = 5
So 963-15-5 is a valid CAS Registry Number.
963-15-5Relevant academic research and scientific papers
Organic semiconductor material and organic electronic device
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Page 21-22, (2010/11/30)
An organic semiconductor material comprising a compound which has a generalized porphyrin skeleton and which has a molecular structure such that the distance from the generalized porphyrin ring plane to the center of each atom forming the generalized porp
An alternative, inexpensive preparation of phenylsulfonylethylene
Cossu, Sergio,De Lucchi, Ottorino,Durr, Richard,Fabris, Fabrizio
, p. 211 - 216 (2007/10/03)
The reaction of (Z)-1,2-bis(phenylsulfonyl)ethylene with tributyltin hydride gives quantitatively phenylsulfonylethylene and constitutes an alternative and inexpensive preparation of this widely used reagent. The reaction also occurs with silicon hydrides (Pd catalyst) and sodium borohydride but the former reaction is not as clean as with tin hydridese while the latter gives the over reduced product phenylsulfonylethane.
