194725-10-5 Usage
Derivative of furan
Contains a furan ring with a sulfur atom and a hydrogen atom attached
Contains a phenyl group
A benzene ring with a substituent group attached
Used in production of pharmaceuticals and fragrances
Due to its chemical structure and properties, it can be used as a building block for creating various compounds
Potential applications in treatment of medical conditions
Has been studied for its potential use in treating neurological disorders and cancer
Investigated for antibacterial and antioxidant properties
Has been researched for its ability to inhibit bacterial growth and its potential to neutralize harmful free radicals
Important compound in medicinal chemistry
Due to its potential applications and versatility in creating various compounds, it is considered an important compound in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 194725-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,7,2 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 194725-10:
(8*1)+(7*9)+(6*4)+(5*7)+(4*2)+(3*5)+(2*1)+(1*0)=155
155 % 10 = 5
So 194725-10-5 is a valid CAS Registry Number.
194725-10-5Relevant articles and documents
Degradable vinyl copolymers through thiocarbonyl addition-ring-opening (TARO) polymerization
Bingham, Nathaniel M.,Roth, Peter J.
, p. 55 - 58 (2019)
The radical copolymerization of the thionolactone dibenzo[c,e]oxepane-5-thione with acrylates, acrylonitrile, and N,N-dimethylacrylamide afforded copolymers containing a controllable amount of backbone thioesters which could be selectively cleaved. The pr
Reaction of thionolactones with zinc enolate: New synthesis of vinylogous carbonates
Lee, Hyeon Kyu,Kim, Jia,Pak, Chwang Siek
, p. 6267 - 6270 (2007/10/03)
Reaction of various thionolactones, prepared from the lactones and Lawesson's reagent, with methyl bromozinc-acetate afforded the corresponding vinylogous carbonates in good yields under mild conditions.
