64502-69-8

Basic information

• Product Name: 1,2,4-Dithiazol-1-ium, 3,5-diphenyl-, perchlorate
• CAS NO: 64502-69-8
• Molecular Formula: C14H10NS2.ClO4
• Molecular Weight: 355.823
• Mol File: 64502-69-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2,4-Dithiazol-1-ium, 3,5-diphenyl-, perchlorate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-Dithiazol-1-ium, 3,5-diphenyl-, perchlorate(64502-69-8)
• EPA Substance Registry System: 1,2,4-Dithiazol-1-ium, 3,5-diphenyl-, perchlorate(64502-69-8)

Safety Data

• Hazardous Substances Data: 64502-69-8(Hazardous Substances Data)

Upstream product

• 2032-36-2 Thiobenzmorpholid 
• 2227-79-4 benzenecarbothioamide 

Downstream Products

• 91850-59-8 N-[1-Phenyl-1-pyrrolidin-1-yl-meth-(Z)-ylidene]-thiobenzamide 
• 80282-58-2 2,4-diphenylthiazole-5-carbonitrile 
• 64499-36-1 4-(4-Methoxyphenylamino)-2,6-diphenyl-5-pyrimidincarbonitril 
• 13996-08-2 4,6-diphenyl-2-thioxo-1,2-dihydropyrimidine-3-carbonitrile 
• 4194-36-9 N-<(Phenylthioxo)-methyl>benzamide 
• 104555-96-6 C₃₈H₃₀N₄O₄S₂ 
• 83610-02-0 3,4-Dihydro-2,6-diphenyl-4-thioxo-5-pyrimidincarbonsaeure-ethylester 
• 37009-52-2 ethyl 2,4-diphenyl-1H-imidazole-5-carboxylate 
• 737-54-2 6-oxo-2,4-diphenyl-1,6-dihydro-pyrimidine-5-carbonitrile 
• 13996-08-2 5-cyano-2,6-diphenylpyrimidine-4(3H)thione 
• 96530-65-3 2-Cyano-3-phenyl-3-thiobenzamidopropenenitrile 
• 83610-02-0 5-ethoxycarbonyl-4-mercapto-2,6-diphenylpyrimidine 
• 101185-06-2 2-Cyan-3-phenyl-3-thiobenzoylamido-acrylsaeureethylester 
• 51803-15-7 5-benzoyl-4-hydroxy-2,6-diphenylpyrimidine 

Relevant articles and documents

The Triethylamine Catalyzed Reaction of N,N-Disubstituted Thioamide-Bromine Adducts With Unsubstituted Thiobenzamide

The reaction of N,N-disubstituted thioamide-bromine adducts with unsubstituted thioamide, followed by treatment with triethylamine, affords novel N'-thiobenzoylamidines along with smaller amounts of secondary products.A mechanism is proposed for the formation of the amidines.The results give an insight into the initial steps of the mechanism by which thioamides are converted into 1,2,4-thiadiazoles.