114751-76-7Relevant articles and documents
Synthesis of N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol- 2(3H)-yl)acetamide derivatives promoted by carbodiimide condensation
Yu, Peng,Hu, Jun,Wan, Rong,Li, Xi,Zheng, Shanlong,Xu, Yanhua
, p. 347 - 350 (2014/07/08)
Novel N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol-2(3H)-yl) acetamide derivatives were prepared by 1-(3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride and N-hydroxybenzotrizole condensation catalysis in a convenient and fast method
LIQUID-CRYSTALLINE IMIDAZO-1,3,4-THIADIAZOLES. I. SYNTHESIS OF 2,6-DISUBSTITUTED IMIDAZO-1,3,4-THIADIAZOLES AND THEIR MESOMORPHOUS AND SPECTRAL CHARACTERISTICS
Torgova, S. I.,Abolin, A. G.,Karamysheva, L. A.,Ivashchenko, A. V.
, p. 172 - 178 (2007/10/02)
Derivatives of imidazo-1,3,4-thiadiazole possessing a wide temperature range of smectic mesophase were obtained.The introduction of the cyclohexane fragment into the imidazole part of the molecule promotes the appearance of the nematic mesophase.The structure of the new mesogens and of the intermediates in their synthesis were confirmed by the data from IR and (13)C and (1)H NMR spectroscopy.