176380-41-9

Basic information

• Product Name: [1-Furan-2-yl-meth-(E)-ylidene]-[5-(2-methoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-amine
• CAS NO: 176380-41-9
• Molecular Weight: 285.326
• Mol File: 176380-41-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [1-Furan-2-yl-meth-(E)-ylidene]-[5-(2-methoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-amine(CAS DataBase Reference)
• NIST Chemistry Reference: [1-Furan-2-yl-meth-(E)-ylidene]-[5-(2-methoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-amine(176380-41-9)
• EPA Substance Registry System: [1-Furan-2-yl-meth-(E)-ylidene]-[5-(2-methoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-amine(176380-41-9)

Safety Data

• Hazardous Substances Data: 176380-41-9(Hazardous Substances Data)

Upstream product

• 98-01-1 furfural 
• 28004-56-0 2-amino-5-(o-methoxyphenyl)-1,3,4-thiadiazole 

Relevant articles and documents

Synthesis, Spectral, Thermal, and Biological Studies of Adducts of Organotin(IV) Halides with Schiff Bases Derived from 2-Amino-5-(o-methoxyphenyl)-1,3,4-thiadiazole

Some new organotin(IV) complexes of the general formula, RnSnCl4-n·L [where n = 3, R = CH3 or C6H5: n = 2, R=C6H5; L= Schiff bases derived from the condensation of 2-amino-5-(o-methoxyphenyl)-1,3,4-thiadiazole with salicyl-aldehyde (L-1), 2-hydroxy-1-naphthaldehyde (L-2), 2′-hydroxyacetophenone (L-3), benzyl methyl ketone (L-4), acetylacetone (L-5), and 2-furancarbaldehyde (L-6)] have been synthesized and characterized by elemental analyses, molar conductances, electronic, infrared, far-infrared, 1H and 119Sn NMR and Moessbauer spectral studies. Thermal studies of three complexes, viz., Ph3SnCl(L-2), Me3SnCl(L-4), and Ph3SnCl(L-5) have been carried out in the temperature range 25-1000°C using TG, DTG, and DTA techniques. All these complexes decompose gradually with the formation of SnO2 as an end product. In vitro antimicrobial activity of the ligands and their complexes has also been determined against Streptococcus faecalis, Kiebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus Penicillin resistance (2500 units), Candida albicans, Cryptococcus neoformans, Sporotrichum schenckii, Trichophyton mentagrophytes, and Aspergillus fumigatus.