89975-90-6

Basic information

• Product Name: N-(furan-2-ylmethylidene)-1H-1,2,4-triazol-5-amine
• CAS NO: 89975-90-6
• Molecular Formula: C₇H₆N₄O
• Molecular Weight: 162.1487
• Mol File: 89975-90-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 366.2°C at 760 mmHg
• Flash Point: 175.3°C
• Density: 1.42g/cm³
• Vapor Pressure: 1.49E-05mmHg at 25°C
• Refractive Index: 1.688
• CAS DataBase Reference: N-(furan-2-ylmethylidene)-1H-1,2,4-triazol-5-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(furan-2-ylmethylidene)-1H-1,2,4-triazol-5-amine(89975-90-6)
• EPA Substance Registry System: N-(furan-2-ylmethylidene)-1H-1,2,4-triazol-5-amine(89975-90-6)

Safety Data

• Hazardous Substances Data: 89975-90-6(Hazardous Substances Data)

Upstream product

• 98-01-1 furfural 
• 61-82-5 3⁽⁵⁾-amino-1,2,4-triazole 

Downstream Products

• 37716-21-5 5-furan-2-yl-3-phenyl-4-(1H-[1,2,4]triazol-3-yl)-4,5-dihydro-[1,2,4]oxadiazole 

Relevant articles and documents

Synthesis of some triazole schiff base derivatives and their metal complexes under microwave irradiation and evaluation of their corrosion inhibition and biological activity

TWO triazole Schiff base derivatives N-(furan-2-ylmethylene)-1H-1,2,4-triazole-3-amine (FTA), N-(thiophene-2-ylmethylene)-1H-1,2,4-triazole-3-amine (TTA) and their metal complexes Co(II), Ni(II), Cu(II) and Zn(II) were synthesized under microwave irradiation. The structure of these compounds has been investigated by using elemental analysis, FT-IR, UV-Vis spectrometric methods, magnetic susceptibility, mass spectra, NMR, ESR and thermal studies. The antimicrobial activities of the prepared ligands and their respective Zn (II) complexes were studied against the bacterial (positive and negative) grams and fungal strains. The inhibitive characteristics of Schiff base ligands on C-steel corrosion in hydrochloric acid were studied using weight loss measurements. The prepared Schiff base derivatives show high inhibition efficiency and their adsorption surface was found to obey Langmuir model. The data also revealed that FTA is less than TTA in terms of inhibiting efficiency.

Comparative study of conventional and microwave-assisted synthesis of some Schiff bases and their potential as antimicrobial agents

A series of Schiff bases (compounds 1-10) were synthesized by condensing heterocyclic/aromatic aldehydes with heterocyclic/aromatic amines through both, conventional method and microwave-assisted synthesis. The compounds were confirmed by means of IR spec