《Reaction of 4-chloropyrimidines with alkylisothioureas》 was written by Hurst, Derek T.. Application of 52854-14-5 And the article was included in Journal of Heterocyclic Chemistry on April 30 ,1995. The article conveys some information:
Reaction of 4,6-dichloro-5-nitropyrimidine with S-methylisothiouronium sulfate gave 1-(4-chloro-5-nitropyrimidinium-6-yl)-S-methylisothiourea by an unusual nucleophilic attack involving an isothiouronium nitrogen atom. Rearrangement of S-Methylisothiuronium sulfate with 4,6-dichloro-5-nitropyrimidine gave [4-(methylthio)-1,3,5-triazin-2(1H)-ylidene]nitroacetonitrile (>70% yield) and 4,6-bis(methylthio)-5-nitropyrimidine (6% yield). In the experiment, the researchers used many compounds, for example, 4-Chloro-6-methoxy-5-nitropyrimidine(cas: 52854-14-5Application of 52854-14-5)
4-Chloro-6-methoxy-5-nitropyrimidine(cas: 52854-14-5) is a member of organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. They are generally not present in crude oils and are typically the result of additives, cleaning solutions or chemicals used for oil recovery.Application of 52854-14-5
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia