1628-53-1

Basic information

• Product Name: 4,5-Thiazoledione, 2-phenyl-
• Synonyms: 2-phenyl-2-thiazoline-4,5-dione;2-phenylthiazole-4,5-dione;2-Phenylthiazolin-4,5-dion;2-phenylthiazoline-4,5-dione;2-phenylthiazolin-4,5-dione
• CAS NO: 1628-53-1
• Molecular Formula: C9H5NO2S
• Molecular Weight: 191.21
• Mol File: 1628-53-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4,5-Thiazoledione, 2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-Thiazoledione, 2-phenyl-(1628-53-1)
• EPA Substance Registry System: 4,5-Thiazoledione, 2-phenyl-(1628-53-1)

Safety Data

• Hazardous Substances Data: 1628-53-1(Hazardous Substances Data)

Upstream product

• 79-37-8 oxalyl dichloride 
• 2227-79-4 benzenecarbothioamide 

Downstream Products

• 14563-09-8 3-cyclohexyl-2,6-diphenyl-2,3-dihydro-[1,3,5]thiadiazin-4-one 
• 14658-14-1 3-(4-methoxy-phenyl)-2,6-diphenyl-2,3-dihydro-[1,3,5]thiadiazin-4-one 
• 13514-41-5 2-phenyl-(4at,8at)-4a,5,8,8a-tetrahydro-5r,8c-methano-benzo[e][1,3]thiazin-4-one 
• 13514-40-4 2-phenyl-(4at,8at)-4a,5,6,7,8,8a-hexahydro-5r,8c-methano-benzo[e][1,3]thiazin-4-one 
• 14563-15-6 2-(4-nitro-phenoxy)-6-phenyl-[1,3,5]thiadiazin-4-one 
• 40012-69-9 2-(naphthalen-1-yl-phenyl-methylene)-4-phenyl-[1,3,5]oxathiazin-6-one 
• 40012-68-8 4-phenyl-2-(2,4,6-trimethyl-benzhydrylidene)-[1,3,5]oxathiazin-6-one 
• 40012-71-3 [10-(6-oxo-4-phenyl-6H-[1,3,5]oxathiazin-2-ylidene)-10H-anthracen-9-ylidene]-δ²-methanone 
• 178408-15-6 N,N-diisobutyl-N'-benzoylthiourea 
• 178408-14-5 tert-butyl ester of N-thiobenzoyloxalamic acid 
• 109988-51-4 1-tert-Butyl-2-ethoxy-2-phenyl-5-thioxo-imidazolidin-4-one 
• 40039-45-0 2,5,5-triphenyl-[1,3]thiazine-4,6-dione 
• 3553-61-5 thiobenzoyl isocyanate 
• 72674-77-2 7-imino-2-phenyl-5-thiobenzoyl-[1,3,5]thiadiazepine-4,6-dione 

Relevant articles and documents

Facile synthesis of 2-azaazulenes from thiobenzoyl isocyanates using trimethylsilyldiazomethane

The reaction of trimethylsilyldiazomethane with thiobenzoyl isocyanates, in situ generated from thiazole-4,5-diones, yielded diazoketones, which were converted into 2-azaazulenes by the intramolecular Buchner reaction.