620158-95-4 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-Chlorophenyl)-6-ethylsulfanyl-2,3-dihydrothiopyran-4-one is used as a potential active pharmaceutical ingredient for its unique structural features that may offer novel therapeutic properties. Its chemical composition could be exploited in the development of new drugs, particularly in areas where its specific functional groups could interact with biological targets.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-Chlorophenyl)-6-ethylsulfanyl-2,3-dihydrothiopyran-4-one may serve as a precursor or intermediate in the synthesis of new pesticides or herbicides. Its structure could provide a basis for the creation of compounds with enhanced efficacy or selectivity in controlling agricultural pests and weeds, while minimizing environmental impact.
Used in Chemical Research:
2-(4-Chlorophenyl)-6-ethylsulfanyl-2,3-dihydrothiopyran-4-one is used as a research compound in academic and industrial laboratories. Its complex structure makes it an interesting subject for studies in organic chemistry, potentially leading to new insights into synthesis methods, reaction mechanisms, or the discovery of new chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 620158-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,5 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 620158-95:
(8*6)+(7*2)+(6*0)+(5*1)+(4*5)+(3*8)+(2*9)+(1*5)=134
134 % 10 = 4
So 620158-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H13ClOS2/c1-2-16-13-8-11(15)7-12(17-13)9-3-5-10(14)6-4-9/h3-6,8,12H,2,7H2,1H3
620158-95-4Relevant academic research and scientific papers
[5C + 1S] annulation: A facile and efficient synthetic route toward functionalized 2,3-dihydrothiopyran-4-ones
Bi, Xihe,Dong, Dewen,Li, Yan,Liu, Qun,Zhang, Qian
, p. 10886 - 10889 (2007/10/03)
A facile and efficient synthetic route toward highly substituted 2,3-dihydrothiopyran-4-ones 2 has been developed via a formal [5C + 1S] annulation of readily available α-alkenoyl ketene-(S,S)-acetals 1 with sodium sulfide nonahydrated salt (Na2/sub
