114710-76-8

Basic information

• Product Name: 3-Allyl-2-[(Z)-phenylimino]-thiazolidin-4-one
• Synonyms: 3-Allyl-2-[(Z)-phenylimino]-thiazolidin-4-one
• CAS NO: 114710-76-8
• Molecular Weight: 232.306
• Mol File: 114710-76-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-Allyl-2-[(Z)-phenylimino]-thiazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Allyl-2-[(Z)-phenylimino]-thiazolidin-4-one(114710-76-8)
• EPA Substance Registry System: 3-Allyl-2-[(Z)-phenylimino]-thiazolidin-4-one(114710-76-8)

Safety Data

• Hazardous Substances Data: 114710-76-8(Hazardous Substances Data)

Upstream product

• 7341-63-1 1-allyl-3-phenyl-thiourea 
• 105-39-5 chloroacetic acid ethyl ester 
• 62-53-3 aniline 
• 102936-66-3 3-Cyclohexyl-2-[(Z)-phenylimino]-thiazolidin-4-one 
• 1219-96-1 N¹-phenyl-N²-(p-methoxyphenyl)thiourea 
• 722-03-2 N¹-phenyl-N²-cyclohexylthiourea 
• 103-72-0 phenyl isothiocyanate 
• 32826-80-5 3-(4-methoxy-phenyl)-2-phenylimino-thiazolidin-4-one 
• 7341-63-1 N¹-phenyl-N²-allylthiourea 
• 79-11-8 chloroacetic acid 

Downstream Products

• 39137-27-4 3-allylthiazolidine-2,4-dione 
• 62-53-3 aniline 

Relevant articles and documents

Facile and regioselective synthesis of thiazolidin-4-one derivatives catalyzed by basic ionic liquid [bmim]OH under ultrasonic irradiation

2-Iminothiazolidin-4-one derivatives were synthesized regioselectively in good to high yields by condensation of N,N-disubstituted thioureas and ethyl chloroacetate in the presence of basic ionic liquid [bmim]OH as a catalyst under conventional and ultrasonic irradiation conditions. Under ultrasonic irradiation, the reaction furnished the desired 2-iminothiazolidinones in higher yields (76-87%) and lower reaction times (30-55 min).