107326-19-2

Basic information

• Product Name: 5-phenylthiazolidine
• Synonyms: 5-phenylthiazolidine
• CAS NO: 107326-19-2
• Molecular Weight: 165.259
• Mol File: 107326-19-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-phenylthiazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenylthiazolidine(107326-19-2)
• EPA Substance Registry System: 5-phenylthiazolidine(107326-19-2)

Safety Data

• Hazardous Substances Data: 107326-19-2(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 934-14-5 2-amino-1-phenyl-ethanethiol 
• 1499-00-9 2-phenylaziridine 
• 7568-93-6 2-Amino-1-phenylethanol 
• 13084-09-8 tris-(benzylsulfanyl-methyl)-amine 
• 2218-01-1 1-Phenyl-2-aminoethylthiosulfuric acid 
• 4561-46-0 1-Chloro-1-phenyl-2-aminoethane hydrochloride 

Downstream Products

• 155914-64-0 3-(benzoylmethyl)-5-phenylthiazolidine 

Relevant articles and documents

Sequential ring expansion and ketene elimination reactions in the novel rhodium(I)-catalyzed carbonylation of thiazolidines

1,3-Thiazolidines react with carbon monoxide, in the presence of catalytic quantities of chloro(1,5-cyclooctadiene)rhodium(I) dimer and potassium iodide, to give thiazolidinones in 56-88% yields. Reaction in the absence of KI afforded the six-membered ring thiazin-3-one. The rhodium(I) complex can catalyze the quantitative conversion of the thiazin-3-one to the thiazolidinone under carbon monoxide, with ketene as the reaction by-product. The conversion of thiazolidines to thiazolidinones involves a novel regiospecific insertion of carbon monoxide into one of two ring carbon-nitrogen bonds, as well as a metal-catalyzed ketene elimination process.

Cyclization of α- and β-alkylthio-substituted amines possessing positively charged carbon at the nitrogen. A new synthetic method for thiazolidines, thiomorpholines and dihydro-1,4-benzothiazines

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