113486-67-2

Basic information

• Product Name: 3-PHENYL-7H-[1,2,4]TRIAZOLO[3,4-B][1,3,4]THIADIAZIN-6-AMINE
• Synonyms: 3-PHENYL-7H-[1,2,4]TRIAZOLO[3,4-B][1,3,4]THIADIAZIN-6-AMINE;3-PHENYL-7H-[1,2,4]TRIAZOLO[3,4-B][1,3,4]THIADIAZIN-6-YLAMINE;BUTTPARK 4\07-98
• CAS NO: 113486-67-2
• Molecular Formula: C₁₀H₉N₅S
• Molecular Weight: 231.28
• Mol File: 113486-67-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-PHENYL-7H-[1,2,4]TRIAZOLO[3,4-B][1,3,4]THIADIAZIN-6-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-PHENYL-7H-[1,2,4]TRIAZOLO[3,4-B][1,3,4]THIADIAZIN-6-AMINE(113486-67-2)
• EPA Substance Registry System: 3-PHENYL-7H-[1,2,4]TRIAZOLO[3,4-B][1,3,4]THIADIAZIN-6-AMINE(113486-67-2)

Safety Data

• Hazardous Substances Data: 113486-67-2(Hazardous Substances Data)

Upstream product

• 111828-01-4 (4-amino-5-phenyl-4H-1,2,4-triazol-3-ylsulphanyl)-methylenenitrile 
• 107-14-2 chloroacetonitrile 
• 22706-11-2 3-phenyl-4-amino-5-mercapto-1,2,4-triazole 
• 22706-11-2 4-amino-3-phenyl-1H-1,2,4-triazole-5(4H)-thione 

Relevant articles and documents

Novel method for the synthesis of s -triazolo[3,4- b ][1,3,4]thiadiazines

The reaction of 4-amino-3-mercapto-5-phenyl-s-triazole with aromatic or aliphatic ketones containing active -hydrogens as a methyl or methylene group using an acidified acetic acid method afforded the corresponding s-triazolo[3,4-b][1,3,4]thiadiazines. In

SYNTHESIS OF SOME CONDENSED s-TRIAZOLE HETEROCYCLES USING PHASE-TRANSFER CATALYSIS TECHNIQUE

Some condensed heterocyclic systems were obtained by reacting 3-phenyl-4-amino-s-triazole-5-thiol 1 as a dianionic ambident compound containing N- and S- poles with some tetrahalo- and dihalo derivatives as well as α-haloketones and

STUDIES ON 4-AMINO-5-ARYL-1,2,4-TRIAZOLE-3-THIONES

4-Amino-5-aryl-1,2,4-triazole-3-thiones 1 react with phenacylbromide at room temperature to give 2, which could be converted to 3 on reflux. Treatment of 1 with chloroacetonitrile and potassium hydroxide in equimolar ratio and in excess yielded 4 and 6, r

Synthesis of Heterocycles. Part VII . Synthesis and Antimicrobial Activity of Some 7H-s-Triazolothiadiazine and s-Triazolothiadiazole Derivatives

The cyclization of 4-amino-5-aryl-3-cyanomethylthio-1,2,4-triazoles II in the presence of concentrated sulfuric acid yields 7H-6-amino-s-triazolothiadiazines III.Cyclization of 4-amino-5-aryl-1,2,4-triazole-3-thiones I with phenacyl chloride yields 7H-3-aryl-6-phenyl-s-triazolothiadiazines IV.Similarly, compounds I condensed with cyanogen bromide, phenyl isothiocyanate and carbon disulfide to give the corresponding cyclized products 6-amino-3-aryl-s-triazolothiadiazoles V, 3-aryl-6-phenylamino-s-triazolothiadiazoles VI and 3-aryl-s-triazolothiadiazol-6(5H)thiones VII, respectively.Also in the presence of phosphoryl chloride, compounds I underwent cyclization with monocarboxylic acids and oxalic acid to 3,6-diaryl-s-triazolothiadiazole VIII and 6,6'-bis(3-aryl-s-triazolothiadiazoles) IX.The above compounds were screened for their antimicrobial activity.