22278-75-7

Basic information

• Product Name: 1,2,4-Triazin-5(2H)-one, 4-amino-6-[(4-chlorophenyl)methyl]-3,4-dihydro-3-thioxo-
• CAS NO: 22278-75-7
• Molecular Formula: C10H9ClN4OS
• Molecular Weight: 268.727
• Mol File: 22278-75-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,2,4-Triazin-5(2H)-one, 4-amino-6-[(4-chlorophenyl)methyl]-3,4-dihydro-3-thioxo-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-Triazin-5(2H)-one, 4-amino-6-[(4-chlorophenyl)methyl]-3,4-dihydro-3-thioxo-(22278-75-7)
• EPA Substance Registry System: 1,2,4-Triazin-5(2H)-one, 4-amino-6-[(4-chlorophenyl)methyl]-3,4-dihydro-3-thioxo-(22278-75-7)

Safety Data

• Hazardous Substances Data: 22278-75-7(Hazardous Substances Data)

Upstream product

• 3617-01-4 β-(4-chlorophenyl)pyruvic acid 
• 2231-57-4 Thiocarbohydrazide 
• 93634-55-0 (Z)-4-(4-chlorobenzylidene)-2-methyloxazol-5(4H)-one 
• 93634-55-0 2-methyl-4-(4-chlorobenzylidene)-4H-oxazol-5-one 
• 104-88-1 4-chlorobenzaldehyde 
• 88681-63-4 2-acetamido-3-(4-chlorophenyl)acrylic acid 

Downstream Products

• 202651-01-2 4-{[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-amino}-6-(4-chloro-benzyl)-3-mercapto-4H-[1,2,4]triazin-5-one 
• 202650-99-5 6-(4-Chloro-benzyl)-3-mercapto-4-{[1-p-tolyl-meth-(E)-ylidene]-amino}-4H-[1,2,4]triazin-5-one 
• 1105064-89-8 C₂₀H₁₅ClN₆O₄S 
• 1105064-94-5 C₂₁H₁₇ClN₆O₄S 
• 1105064-98-9 C₂₁H₁₇ClN₆O₅S 

Relevant articles and documents

Synthesis and antimicrobial activities of a new series of 4-S-[41-amino-51-oxo-61-substituted benzyl-41,51-dihydro-11,21,41-triazin-3-yl]mercaptoacetyl-3-arylsydnones

The synthesis of some 4-S-(41-amino-51-oxo-61-substituted benzyl-41,51-dihydro-11,21,41-triazin-3-yl)mercaptoacetyl-3-arylsydnones by the reaction of 3-aryl-4-bromoacetylsydnones with 6-substituted-4-amino-3-mercapto-1,2,4-triazin-5-ones is described. The IR, 1H NMR, mass spectra and elemental analysis characterized the newly synthesized compounds. The synthesized compounds were screened for their antimicrobial activity. All the compounds showed higher activity than that of standard drug during antimicrobial studies and the activity was comparable with the standard drug for antifungal activity.

Studies on arylmethyltriazinone derivatives-Part II. Synthesis and antifungal properties of 2-aminomethyl-4-(arylidene)amino-6-arylmethyl-3-mercapto-1, 2,4-triazin-5(4H)-ones

The preparation of twenty new 2-aminomethyl-4-(arylidene)amino-6-arylmethyl-3-mercapto-1,2,4-triazin-5(4H)- ones(4) is described. The structural elucidation of all the compounds is carried out on the basis of analytical and spectral data. The newly synthesized compounds are evaluated for their antifungal activity against Candida albicans and Paecileomyces variotti.

Herbicidal agents

3-[HYDROGEN-, (UNSUBSTITUTED AND HALO, AMINO, NITRO, ALKYL, ALKANOYL, ALKOXY, ALKYLMERCAPTO, ARYLOXY AND/OR ARYL-MERCAPTO-SUBSTITUTED) ALIPHATIC-, CYCLOALIPHATIC-, ARALIPHATIC-, ARYL-, OR HETEROCYCLIC- -SUBSTITUTED OXY, MERCAPTO OR AMINO]4-[AMINO; MONO AND DI (UNSUBSTITUTED AND CYANO, HYDROXY AND/OR HALO-SUBSTITUTED) ALKYL- AND/OR ALKANOYL-AMINO; N-heterocyclic; or N-(unsubstituted and aryl, haloaryl, alkoxyaryl, nitroaryl and/or heterocyclic- substituted) alkylidene or cycloalkylidene]-6-[(unsubstituted and halo, nitro, carbo lower alkoxy, alkyl, alkoxy, alkylmercapto, aralkylmercapto, aryloxy and/or arylmercapto-substituted) aliphatic, cycloaliphatic, araliphatic, aryl, or heterocyclic]-1,2,4-triazine-5-ones, which possess herbicidal properties, and which may be produced by conventional methods.