54615-63-3 Usage
Uses
Used in Organic Chemistry:
2-Ethoxy Thiophenol is used as an intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities and materials. Its unique structure allows for versatile reactions and transformations, making it a valuable component in the synthesis process.
Used in Pharmaceutical Industry:
2-Ethoxy Thiophenol is used as a building block in the development of pharmaceutical compounds, potentially leading to the creation of new drugs with therapeutic applications. Its presence in the molecular structure can influence the properties and activities of the final drug product.
Used in Chemical Research:
2-Ethoxy Thiophenol is used as a research tool in chemical studies, helping scientists understand the properties and reactivity of thiophenol-containing compounds. This knowledge can be applied to design more efficient synthetic routes and develop novel compounds with desired characteristics.
Used in Material Science:
2-Ethoxy Thiophenol is used in the development of new materials, such as polymers and coatings, that can benefit from the unique properties of thiophenol-containing structures. Its incorporation into these materials can lead to improved performance and new applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 54615-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,1 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54615-63:
(7*5)+(6*4)+(5*6)+(4*1)+(3*5)+(2*6)+(1*3)=123
123 % 10 = 3
So 54615-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10OS/c1-2-9-7-5-3-4-6-8(7)10/h3-6,10H,2H2,1H3
54615-63-3Relevant articles and documents
Solvent-free synthesis of thiophenol using uncatalyzed transfer hydrogenation
Zhou, Shaodong,Qian, Chao,Chen, Xinzhi
experimental part, p. 2432 - 2439 (2012/06/18)
Clean and sustainable transfer hydrogenation for aryl sulfonamides and sulfonyl chlorides is described. The protocol is chemoselective and uses neither catalyst nor solvent.
Catalytic transfer hydrogenation of aryl sulfo compounds
Chen, Xinzhi,Zhou, Shaodong,Qian, Chao
experimental part, p. 179 - 185 (2012/05/21)
A new method to reduce aryl sulfo compounds via transfer hydrogenation was investigated, using Pd/C as a catalyst, and 2-propanol or formic acid as hydrogen sources. This new process is simple and clean.
Cell adhesion-inhibiting antiinflammatory and immune-suppressive compounds
-
, (2008/06/13)
The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immunune diseases, to pharmaceutical compositions containing these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.
Cell adhesion-inhibiting antiinflammatory and immune-suppressive compounds
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Page 47, (2010/02/07)
The present invention relates to novel cinnamide compounds that are useful for treating inflammatory and immune diseases and cerebral vasospasm, to pharmaceutical compositions containing these compounds, and to methods of inhibiting inflammation or suppressing immune response in a mammal.