Vasudevan, Anil et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2005 | CAS: 55661-33-1

Thiazol-2-ylmethanamine (cas: 55661-33-1) belongs to thiazole derivatives. Thiazole is a five-membered, unsaturated, planar, π-excessive heteroaromatic containing one sulfur atom and one pyridine-type nitrogen atom at position 3 of the cyclic ring system. Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.Recommanded Product: 55661-33-1

Identification of ortho-amino benzamides and nicotinamides as MCHr1 antagonists was written by Vasudevan, Anil;LaMarche, Matthew J.;Blackburn, Christopher;Che, Jennifer Lee;Luchaco-Cullis, Courtney A.;Lai, Sujen;Marsilje, Thomas H.;Patane, Michael A.;Souers, Andrew J.;Wodka, Derek;Geddes, Bradley;Chen, Sumiao;Brodjian, Seven;Falls, Doug H.;Dayton, Brian D.;Bush, Eugene;Brune, Michael;Shapiro, Robin D.;Marsh, Kennan C.;Hernandez, Lisa E.;Sham, Hing L.;Collins, Christine A.;Kym, Philip R.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2005.Recommanded Product: 55661-33-1 This article mentions the following:

Several potent and efficacious MCHr1 antagonists containing an ortho-amino benzamide or nicotinamide chemotype have been identified, exemplified by compounds (I) and (II). In the experiment, the researchers used many compounds, for example, Thiazol-2-ylmethanamine (cas: 55661-33-1Recommanded Product: 55661-33-1).

Thiazol-2-ylmethanamine (cas: 55661-33-1) belongs to thiazole derivatives. Thiazole is a five-membered, unsaturated, planar, π-excessive heteroaromatic containing one sulfur atom and one pyridine-type nitrogen atom at position 3 of the cyclic ring system. Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.Recommanded Product: 55661-33-1

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica