3652-33-3

Usage

Uses

Used in Corrosion Inhibition:
4-Amino-4H-1,2,4-triazole-3,5-dithiol is used as a corrosion inhibitor in various industrial processes. It helps control metal corrosion in different environments, thereby protecting metal structures and equipment from degradation.
Used in Coordination Chemistry:
In coordination chemistry, 4-Amino-4H-1,2,4-triazole-3,5-dithiol serves as a ligand. Its ability to form stable complexes with metal ions makes it valuable for the synthesis of coordination compounds with specific properties and applications.
Used in Chemical Synthesis:
4-Amino-4H-1,2,4-triazole-3,5-dithiol is utilized in the synthesis of other organic compounds. Its unique structure allows it to act as a building block or a reagent in the creation of various chemical products.
Used in Pharmaceutical Research:
4-Amino-4H-1,2,4-triazole-3,5-dithiol has been studied for its potential pharmaceutical properties, such as antioxidant and anti-inflammatory effects. Its biological activities are being explored for possible applications in the development of new drugs and therapies.
Used in Chemical Reagent Production:
4-AMINO-4H-1,2,4-TRIAZOLE-3,5-DITHIOL is also used in the production of chemical reagents. Its versatility and reactivity make it suitable for use in various laboratory and industrial applications, contributing to the synthesis and analysis of other chemicals.

InChI:InChI=1/C2H4N4S2/c3-6-1(7)4-5-2(6)8/h3H2,(H,4,7)(H,5,8)

Upstream product

• 142-46-1 bithiourea 
• 854654-87-8 N,N'-bis-isothiocyanato-thiourea 
• 20953-16-6 1-thiocarbamylthiocarbohydrazide 
• 2231-57-4 Thiocarbohydrazide 
• 75-15-0 carbon disulfide 
• 253266-93-2 4-thioxo-3,5-dithia-heptanedioic acid dimethyl ester 

Downstream Products

• 188896-73-3 4-salicylaldimino-3,5-dimercapto-1,2,4-triazole 
• 760177-52-4 1,2-bis[(4-amino-5-mercapto-1,2,4-triazol-3-yl)mercaptomethyl]benzene 
• 1115025-04-1 5,6-diethoxycarbonyl-3,8-di(4-methylphenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-05-2 5,6-diethoxycarbonyl-3,8-di(4-chlorophenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-06-3 5,6-diethoxycarbonyl-3,8-di(4-nitrophenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-03-0 5,6-diethoxycarbonyl-3,8-diphenyl-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-01-8 5,6-diphenyl-3,8-di(4-nitrophenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-00-7 3,5,6,8-tetraphenyl-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-12-1 5,6-dibenzoyl-3,8-di(4-nitrophenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-11-0 5,6-dibenzoyl-3,8-diphenyl-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-08-5 5,6-diphenylcarbamoyl-3,8-di(4-methylphenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-09-6 5,6-diphenylcarbamoyl-3,8-di(4-chlorophenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-10-9 5,6-diphenylcarbamoyl-3,8-di(4-nitrophenyl)-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 
• 1115025-07-4 5,6-diphenylcarbamoyl-3,8-diphenyl-1,2,3,4,5a,7,8,8b-octaaza-acenaphthylene 

Relevant academic research and scientific papers

Synthesis and characterization of manganese, copper and zinc complexes derived from Schiff - base ligand

A Schiff base has been prepared by the condensation of 4- amino -3,5-dimercapto, 1,2,4-triazole with 2,4-diaminobenzaldehyde. The ligand has been used for complexation with Mn(II), Cu(II) and Zn(II) metal ions. The complexes have been characterized by their elemental analysis, molar conductivity, magnetic susceptibility, IR spectra and electronic spectra. The very low value of molar conductivity of complexes shows their non-electrolytic nature. The comparison of IR spectra of complexes with that of free ligand reveals that the ligand is coordinated through azomethine nitrogen and deprotonated thiol sulphur forming five membered heterochelates. The magnetic moment values and electronic spectral bands clearly indicate the octahedral geometry around metal ions in complexes.

Magnetic and spectral study of some mixed ligand complexes

Complexes of Fe(II), Co(II) and Ni(II) metal ions have been prepared with 4-(phydroxyl benzalidimino)-3,5-dimercapto-1,2,4-triazole (LH) as primary ligand while pyridine has been used as secondary ligand. The analytical data suggest 1:2 (M:L) stoichiometric composition of complexes . The electrical conductivity indicates their non- electrolytic nature. The magnetic and spectral character favour octahedral geometry of Fe(II), Co(II) and Ni(II) complexes.

Regioselective synthesis of 3-sulfanyl-5H-naphtho[2,3-e][1,3,4] triazino[3,4-b][1,3,4]thiadiazole-6,11-dione and its derivatives

Regioselective synthesis of novel 3-sulfanyl-5H-naphtho[2,3-e][1,3,4] triazino[3,4-b][1,3,4]thiadiazole-6,11-dione (3) has been achieved by the condensation of 2-bromo-3-hydroxynaphthalene-1,4-dione (1) with 4-amino-4H-1,2,4-triazole-3,5-dithiol (2) in DM

A highly regioselective synthesis of 8-hydroxy-3-sulfanyl-7-undecyl-5H-[1, 2,4]triazolo[3,4-b][1,3,4]benzothiadiazole-6,9-dione and its derivative

Regioselective synthesis of novel 8-hydroxy-3-sulfanyl-7-undecyl-5 H-[1,2,4]triazolo[3,4-b][1,3,4]benzothiadiazole-6,9-dione (3) by condensation of 2-bromo-3,6-dihydroxy-5-undecyl-1,4-benzoquinone (bromoembelin) (1) with 4-amino-4 H-1,2,4-triazole-3,5-dit