Detail of "66870-61-9"
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- Formation of trisubstituted 1,2,4-triazoles in the cyclodehydration of 2-hydrazinothiazoles
- Formation of trisubstituted 1,2,4-triazoles in the cyclodehydration of 2-hydrazinothiazoles. There are some commonly used reagents like 66870-61-9 in this article. Competition of two reaction routes. Veverka, Miroslav; Svetlik, Jan (Inst. Biotechnol., Slovak Tech. Univ., Bratislava 812 37, Czech.). Liebigs Ann. Chem., (1), 75-7 (English) 1989. CODEN: LACHDL. ISSN: 0170-2041. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) The intramol. cyclodehydration of Et (2-hydrazinothiazol-4-yl)acetates I (R = Ph, Me, 2-furyl, 5-bromo-2-furyl, 5-phenyl-2-furyl, 2-thienyl) with POCl3 has been re-examd. The reactions yield the desired thiazolo[2,3-c]-s-triazoles II together with the unexpected trisubstituted 1,2,4-triazoles III. .


![Molecular Structure of 66870-61-9 (ethyl 2-[2-(2-benzoylhydrazinyl)-1,3-thiazol-4-yl]acetate)](http://www.lookchem.com/300w/33/327017.png)