Synthetic Route of 4983-28-2, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 4983-28-2, Name is 2-Chloro-5-hydroxypyrimidine, SMILES is ClC1=NC=C(C=N1)O, belongs to pyrimidines compound. In a article, author is El-Mahdy, K. M., introduce new discover of the category.
Convenient Methodology for Some Heterocyclization Reactions with Thioxopyrimidine Derivatives
A simple and efficient method for derivatization of the pyrimidine nucleus is developed. The readily available 6-amino-2-thioxo-2,3-dihydropyrimidin-4(1H)-one has been used as a versatile building block for the synthesis of thioxopyrimidine derivatives. A variety of novel fused pyrimidines has been prepared via nucleophilic and/or electrophilic reactions of thioxopyrimidine derivatives. The structures of the newly synthesized products have been deduced on the basis of elemental analysis and spectral data.
Synthetic Route of 4983-28-2, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 4983-28-2.
Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia