4413-42-7

Basic information

• Product Name: 3H-1,2,4-Triazole-3-thione, 4-amino-5-[(2-chlorophenoxy)methyl]-2,4-dihydro-
• CAS NO: 4413-42-7
• Molecular Formula: C9H9ClN4OS
• Molecular Weight: 256.716
• Mol File: 4413-42-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3H-1,2,4-Triazole-3-thione, 4-amino-5-[(2-chlorophenoxy)methyl]-2,4-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-1,2,4-Triazole-3-thione, 4-amino-5-[(2-chlorophenoxy)methyl]-2,4-dihydro-(4413-42-7)
• EPA Substance Registry System: 3H-1,2,4-Triazole-3-thione, 4-amino-5-[(2-chlorophenoxy)methyl]-2,4-dihydro-(4413-42-7)

Safety Data

• Hazardous Substances Data: 4413-42-7(Hazardous Substances Data)

Upstream product

• 614-61-9 (2-chlorophenoxy)acetic acid 
• 2231-57-4 Thiocarbohydrazide 
• 36304-40-2 (2-chlorophenoxy)acetic acid hydrazide 
• 95-57-8 2-monochlorophenol 
• 52094-97-0 ethyl 2-(2-chlorophenoxy)acetate 
• 768323-53-1 N-[(2-chloro-phenoxy)-acetyl]-hydrazinecarbodithioic acid 

Downstream Products

• 14758-90-8 5-(2-Chloro-phenoxymethyl)-4-{[1-(5-nitro-furan-2-yl)-meth-(E)-ylidene]-amino}-4H-[1,2,4]triazole-3-thiol 
• 623936-90-3 5-(2-Chloro-phenoxymethyl)-4-{[1-[5-(4-methoxy-2-nitro-phenyl)-furan-2-yl]-meth-(E)-ylidene]-amino}-2,4-dihydro-[1,2,4]triazole-3-thione 
• 682769-41-1 3-[4-amino-5-(2-chloro-phenoxymethyl)-4H-[1,2,4]triazol-3-ylsulfanyl]-3-(5-nitro-furan-2-yl)-1-phenyl-propenone 
• 682769-49-9 3-[4-amino-5-(2-chloro-phenoxymethyl)-4H-[1,2,4]triazol-3-ylsulfanyl]-3-(5-nitro-furan-2-yl)-1-p-tolyl-propenone 
• 1258254-27-1 C₁₉H₁₄Cl₂N₆OS 
• 1258254-28-2 C₁₉H₁₄ClFN₆OS 
• 1258254-29-3 C₁₅H₁₅ClN₆OS 
• 1214892-00-8 C₁₈H₁₀Cl₂N₄OS₂ 

Relevant articles and documents

Synthesis and?studies on?some?new fluorine containing triazolothiadiazines as?possible antibacterial, antifungal and?anticancer agents

Synthesis of a series of 7-arylidene-6-(2,4-dichlorophenyl)-3-aryloxymethyl/anilinomethyl-1,2,4-t riazolo[3,4-b]-1,3,4-thiadiazines (3) by the condensation of 3-aryl-1-(2,4-dichloro-5-fluorophenyl)-2-bromo-propen-1-one (1) and 4-amino-5-mercapto-3-aryloxy

Synthesis and antibacterial activity of N-bridged heterocycles derived from aryloxymethyltriazoles

Reactions of 3-aryloxymethyl-4-amino-5-mercapto-1,2,4-triazoles 1 with aromatic carboxylic acids, furoic acid, oxalic acid, monochloroacetic acid and phenacyl bromide furnish various N-bridged heterocycles viz., triazolothiadiazoles, bistriazolothiadiazoles, triazolothiadiazinones and triazolothiadiazines. The structures of these N-bridged heterocycles are characterized on the basis of elemental analyses, IR, NMR and mass spectral data. Some of these compounds are also subjected to antibacterial screening studies.