62459-17-0 Usage
Chemical structure
2-(benzylsulfanyl)-6-phenyl-4(3H)-pyrimidinone consists of a pyrimidine backbone with a substituted benzylsulfanyl group.
Type of compound
Heterocyclic compound, as it contains a pyrimidine ring (a heterocyclic ring with nitrogen atoms).
Potential applications
Pharmacological, due to its structural features.
Biological activities
May exhibit biological activities, making it a potential candidate for drug development.
Benzylsulfanyl group
The presence of this group may impart specific chemical and biological properties to the compound, making it of interest for further study and potential therapeutic use.
Check Digit Verification of cas no
The CAS Registry Mumber 62459-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,5 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62459-17:
(7*6)+(6*2)+(5*4)+(4*5)+(3*9)+(2*1)+(1*7)=130
130 % 10 = 0
So 62459-17-0 is a valid CAS Registry Number.
62459-17-0Relevant academic research and scientific papers
Development of an efficient and straightforward methodology toward the synthesis of molecularly diverse 2,6-disubstituted 3,4-dihydropyrimidin-4(3H)-ones
Font, David,Heras, Montserrat,Villalgordo, Jose? M.
, p. 1833 - 1842 (2007/10/03)
A simple and efficient methodology toward the synthesis of highly molecularly diverse 2,6-disubstituted 3,4-dihydropyrimidin-4(3H)-ones of type 3 has been developed. The methodology is based on a selective O-alkylation reaction with i-PrOH under Mitsunobu conditions followed by a nucleophilic heteroaromatic ipso-substitution of sulfones 20 and subsequent acidic hydrolysis of the isopropoxy group.
