6200-49-3

Basic information

• Product Name: N-phenyl-N-(3-phenyl-1,3-thiazolidin-2-ylidene)amine
• Synonyms: N-phenyl-N-(3-phenyl-1,3-thiazolidin-2-ylidene)amine
• CAS NO: 6200-49-3
• Molecular Formula: C₁₅H₁₄N₂S
• Molecular Weight: 254.35006
• Mol File: 6200-49-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-phenyl-N-(3-phenyl-1,3-thiazolidin-2-ylidene)amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-N-(3-phenyl-1,3-thiazolidin-2-ylidene)amine(6200-49-3)
• EPA Substance Registry System: N-phenyl-N-(3-phenyl-1,3-thiazolidin-2-ylidene)amine(6200-49-3)

Safety Data

• Hazardous Substances Data: 6200-49-3(Hazardous Substances Data)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 107-06-2 1,2-dichloro-ethane 
• 62-53-3 aniline 
• 122-98-5 2-Anilinoethanol 
• 696-18-4 1-phenylaziridine 
• 106-93-4 ethylene dibromide 
• 96-49-1 [1,3]-dioxolan-2-one 
• 2654-05-9 1-(2-hydroxy-ethyl)-1,3-diphenyl-thiourea 
• 201943-51-3 1,2-diphenylisothiocarbamidoethane 
• 3898-08-6 1,1-diphenylthiourea 

Relevant articles and documents

Synthesis of thiazolidinimines/thiazinan-2-imines via three-component coupling of amines, vic-dihalides and isothiocyanates under metal-free conditions

An expeditious approach for the synthesis of thiazolidin-2-imines and 1,3-thiazinan-2-imines through three-components coupling (TCC) of amines, isothiocynates and dihalides under metal-free conditions has been described. Dichloroethane (DCE) employed as two carbon (C2) source for the annulation and obtained saturated five membered heterocycles.With 1,3-dibromopropane, six membered heterocycles were obtained in good yields. The metal-free, broad substrate scope, functional group tolerance and applicability at gram scale synthesis are the advantages of the present protocol.

The Preparation of Cyclic Dithia and Thiaza Compounds by the Reaction of Potassium Carbonate with Heterocumulenes and Alkylene Dibromides or Carbonate Catalyzed by Organostannyl Compounds

Cyclic 1,3-dithia- and 1,3-thiaza-2-ylidene compounds were obtained by the heterogenous reaction of solid potassium carbonate, a sulfur-containing heterocumulene, such as aryl isothiocyanate, carbon disulfide, or carbonyl silfide, and alkylene dibromides or ethylene carbonate in the presence of bis(tributylstannyl) compounds.The effect of an organostannyl catalyst on these reactions is discussed.