Archives for Chemistry Experiments of 150728-13-5

Synthetic Route of 150728-13-5, 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 150728-13-5.

Synthetic Route of 150728-13-5, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 150728-13-5, Name is 4,6-Dichloro-5-(2-methoxyphenoxy)-2,2′-bipyrimidine, SMILES is ClC1=NC(=NC(=C1OC2=C(C=CC=C2)OC)Cl)C3=NC=CC=N3, belongs to pyrimidines compound. In a article, author is Gein, V. L., introduce new discover of the category.

Synthesis, Structure, and Antibacterial Activity of Alkyl 6-Aroyl-7-aryl-4,7-dihydrotetrazolo[1,5-a]pyrimidine-5-carboxylates

A series of new alkyl 6-aroyl-7-aryl-4,7-dihydrotetrazolo[1,5-a]pyrimidine-5-carboxylates was obtained through the three-component reaction of alkyl esters aroylpyruvic acids with a mixture of aromatic aldehyde and 5-aminotetrazole. All the synthesized compounds were tested for antibacterial activity.

Synthetic Route of 150728-13-5, 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 150728-13-5.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia