Nagaraju, Tumula published the artcilePhI(OAc)2-Mediated Regioselective Synthesis of 5-Guanidino-1,2,4-thiadiazoles and 1,2,4-Triazolo[1,5-a]pyridines via Oxidative N-S and N-N Bond Formation, HPLC of Formula: 3696-23-9, the publication is Synthesis (2019), 51(19), 3600-3610, database is CAplus.
An effective and expeditious approach for the construction of biol. important 5-guanidino-1,2,4-thiadiazoles I [R1 = n-Pr, Ph, 3-ClC6H4, etc.; R2 = Ph, 2-MeOC6H4, 4-ClC6H4, etc.] and 1,2,4-triazolo[1,5- a]pyridine derivatives II [R3 = H, 7-Me, 7-Cl; R4 = Ph, 2-thienyl, 3-O2NC6H4, etc.] were developed with high efficiency and excellent regioselectivity. This new protocol involved the phenyliodine(III) diacetate-mediated oxidative cyclization of thioureas/2-aminopyridines and imidates via N-S and N-N bond formation at ambient temp to afford target compounds I and II resp.
Synthesis published new progress about 3696-23-9. 3696-23-9 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Thiourea,Amine,Benzene,Amide, name is 1-(4-Chlorophenyl)thiourea, and the molecular formula is C7H7ClN2S, HPLC of Formula: 3696-23-9.
Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics