66181-18-8

Upstream product

• 2002-03-1 2-amino-5-phenyl-1,3,4-thiadiazole 
• 333-20-0 potassium thioacyanate 
• 1147550-11-5 ammonium thiocyanate 
• 65-85-0 benzoic acid 
• 66181-13-3 4-(5-phenyl-[1,3,4]thiadiazol-2-yl)-3-thio-allophanic acid methyl ester 

Downstream Products

• 89335-17-1 2-[(Z)-5-Phenyl-[1,3,4]thiadiazol-2-ylimino]-thiazolidin-4-one 
• 1021423-02-8 C₁₃H₁₂N₄OS₂ 
• 1021422-96-7 C₁₂H₁₀N₄OS₂ 

Relevant academic research and scientific papers

Synthesis and antimicrobial activities of thiadiazole containing quinoline derivatives

A novel series of 1-[(substituted 2-chloroquinolin-3-yl)methylidene]-3-[substituted-5-phenyl-1,3,4-thiadiazol-2-yl] thioureas have been synthesized by acid catalyzed reaction between the 1-(5-substitued phenyl-1,3,4-thiadiazol-2-yl) thioureas and 6-substi

GUANIDINE COMPOUNDS, AND USE THEREOF AS BINDING PARTNERS FOR 5-HT5 RECEPTORS

The invention relates to guanidine compounds of general formula (I), corresponding enantiomeric, diastereomeric, and/or tautomeric forms thereof, and pharmaceutically acceptable salts thereof. The invention further relates to the use of guanidine compounds as binding partners for 5-HT5 receptors in order to treat diseases modulated by 5-HT5 receptor activity, especially treat neurodegenerative and neuropsychiatric disorders and the signs, symptoms, and malfunctions associated therewith.

Synthesis and fungicidal activity of some 5-methylene-2-amino-4-thiazolones

N1 (5-Aryl-1,3,4-oxa (thia) diazol-2-yl)thioureas (1a-f) undergo regioselective cyclocondensation with 2,3-dibromopropionyl chloride (2) to give 5-methylene-2--amino-4-thiazolones (4a-f).These compounds