141075-87-8 Usage
Description
Benzene, [(1-fluoroethenyl)thio]-, also known as [(1-Fluoroethenyl)thio]benzene, is an organic compound with a unique structure that features a benzene ring with a fluoroethenylthio group attached to it. Benzene, [(1-fluoroethenyl)thio]is characterized by its potential carcinogenic properties due to its classification as a polycyclic aromatic hydrocarbon (PAH) and its unique electrical and optical properties as a conjugated macromolecule.
Uses
Used in Chemical Synthesis:
Benzene, [(1-fluoroethenyl)thio]is used as an intermediate in the synthesis of 13-Fluorodibenzo[a,i]pyrene (F588440), a compound with potential applications in various chemical and pharmaceutical industries. The synthesis process involves the activation of P450 mono-oxygenase enzymes, which play a crucial role in the metabolism and detoxification of various compounds.
Used in Research and Development:
Due to its unique electrical and optical properties, Benzene, [(1-fluoroethenyl)thio]can be utilized in the development of novel materials and devices in the fields of electronics, optoelectronics, and photonics. Its conjugated macromolecular structure allows for the exploration of its potential in creating advanced materials with improved performance and functionality.
Used in Environmental and Health Studies:
As a polycyclic aromatic hydrocarbon (PAH), Benzene, [(1-fluoroethenyl)thio]can be used in research aimed at understanding the environmental and health impacts of PAHs. This includes studying their carcinogenic properties, their behavior in the environment, and their potential effects on human health.
Used in Pharmaceutical Industry:
Although Benzene, [(1-fluoroethenyl)thio]itself may not be directly used as a pharmaceutical compound, its synthesis intermediate, 13-Fluorodibenzo[a,i]pyrene (F588440), could potentially be utilized in the development of new drugs or drug candidates. Further research and development in this area could lead to the discovery of novel therapeutic agents with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 141075-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,7 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141075-87:
(8*1)+(7*4)+(6*1)+(5*0)+(4*7)+(3*5)+(2*8)+(1*7)=108
108 % 10 = 8
So 141075-87-8 is a valid CAS Registry Number.
141075-87-8Relevant articles and documents
Fluorovinyl Thioethers as Putative Steric and Electronic Thioester Enolate Mimetics: Chemoselective HF Addition to Acetylene Thioethers
Bello, Davide,Cormanich, Rodrigo A.,O'Hagan, David
, p. 72 - 79 (2015)
Fluorovinyl thioethers are presented as a putative biomimetic surrogate for the enol/ate of a thioester. A method is explored for the preparation of fluorovinyl thioethers by treatment of acetylene thioethers with pyridinium (poly)-hydrogen fluoride. Titr
Synthesis and reactivity of (1-fluorovinyl) phenyl sulfoxide as a dienophile
Hanamoto, Takeshi,Korekoda, Kaoru,Nakata, Kenya,Handa, Kumiko,Koga, Yukinori,Kondo, Michio
, p. 99 - 101 (2007/10/03)
(1-Fluorovinyl) phenyl sulfoxide 2 was prepared in two steps from (1-fluorovinyl)methyldiphenylsilane. Although the sulfoxide 2 underwent Diels-Alder reaction with very reactive diene, 1,3-diphenylisobenzofuran, to give the corresponding fluorinated-napht
