Development of s-triazine anticytokinins and their quantitative structure-activity relationship was written by Shimizu, Ryo;Iwamura, Hajime;Matsubara, Satoshi;Fujita, Toshio. And the article was included in Journal of Agricultural and Food Chemistry in 1989.Electric Literature of C9H6Cl2N4 The following contents are mentioned in the article:
A new, nonadenylate series of anticytokinins, N2-substituted 2-amino-4-chloro-6-(ethylamino)-s-triazines, has been developed. The activity in terms of the I50 value of the most potent members was (0.3-0.5) × 10-6M when examined by the tobacco (Nicotiana tabacum) callus assay in the presence of 0.05 × 10-6 M kinetin. The design of the mol. was made on the basis of insight into the active structure obtained from a cytokinin receptor map drawn previously. Quant. anal. of their structure-activity relationship showed that the mode of their binding to the receptor was in important ways the same as for previously known anticytokinins, the structure of which resembles the adenylate cytokinins. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Electric Literature of C9H6Cl2N4).
4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Electric Literature of C9H6Cl2N4
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics