Simple exploration of 2,3-Dichloroquinoxaline

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 2213-63-0, and how the biochemistry of the body works.Electric Literature of 2213-63-0

Electric Literature of 2213-63-0, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2. In a Article£¬once mentioned of 2213-63-0

BRIDGEHEAD NITROGEN HETEROCYCLES. PART III. SYNTHESIS OF FUSED HETEROCYCLES FROM 3-(2,4-DICHLOROPHENYL)-5-MERCAPTO-1,2,4-s-TRIAZOLES

The condensation reaction of 3-(2,4-dichlorophenyl)-5-mercapto-1,2,4-s-triazole with chloroacetic acid, aromatic aldehydes, oxalyl chloride, dimethyl acetylenedicarboxylate, 1,2-diaminocompounds and 1,2-diketones leading to the formation of fused heterocycles was carried out.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 2213-63-0, and how the biochemistry of the body works.Electric Literature of 2213-63-0

Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1336 | ChemSpider