《Synthesis and thermal transformations of 5-nitropyrimidin-4-yl dialkyldithiocarbamates》 was written by Ryabova, O. B.; Makarov, V. A.; Chernyshev, V. V.; Granik, V. G.. Application In Synthesis of 4-Chloro-6-methoxy-5-nitropyrimidine And the article was included in Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya) on April 30 ,2004. The article conveys some information:
On heating, 5-nitropyrimidin-4-yl dialkyldithiocarbamates undergo two types of transformations. One type of these transformations involves intramol. ipso-substitution of the nitro group to form bis(4-dialkylcarbamoylthiopyrimidin-5-yl) disulfides, whereas another type of transformations involves elimination of carbon disulfide to give 4,6-diamino-5-nitropyrimidine derivatives The reaction pathway is controlled by the steric effect of the substituent at position 6 of the pyrimidine ring.4-Chloro-6-methoxy-5-nitropyrimidine(cas: 52854-14-5Application In Synthesis of 4-Chloro-6-methoxy-5-nitropyrimidine) was used in this study.
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 In Synthesis of 4-Chloro-6-methoxy-5-nitropyrimidine
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia