62459-06-7 Usage
Molecular Structure
Pyrimidine derivative with an allylthio group and a methyl group
Potential Uses
Antiviral and anticancer agent, antioxidant, neuroprotective agent, and anti-inflammatory agent
Mechanism of Action
Inhibition of an enzyme involved in viral replication and tumor cell growth
Current Status
Ongoing research and development for potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62459-06-7 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, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62459-06:
(7*6)+(6*2)+(5*4)+(4*5)+(3*9)+(2*0)+(1*6)=127
127 % 10 = 7
So 62459-06-7 is a valid CAS Registry Number.
62459-06-7Relevant articles and documents
Synthesis of 2-alkyl(aralkyl)sulfanyl-6-methylpyrimidin-4(3H)-ones and 4-alkyl(aralkyl)oxy-2-alkyl(aralkyl)sulfanyl-6-methylpyrimidines
Rakhimov,Titova
, p. 96 - 102 (2007/10/03)
2-Alkyl(aralkyl)sulfanyl-6-methylpyrimidin-4(3H)-ones and 4-alkyl(aralkyl)oxy-2-alkyl(aralkyl)-sulfanyl-6-methylpyrimidines having similar or different substituents on the sulfur and oxygen atoms were synthesized by alkylation of sodium salts derived from
IODOCYCLIZATION OF 2-ALLYLTHIO-4(3H)-PYRIMIDINONES
Kim, D. G.,Shmygarev, V. I.
, p. 183 - 185 (2007/10/03)
It has been established that the iodocyclization of 2-allylthio-4(3H)-pyrimidinones occurs at the N(1) nitrogen atom with the formation of 3-iodomethyl-7-oxo-2,3-dihydro-8H-thiazolopyrimidinium iodides and triiodides.
