32826-80-5

Basic information

• Product Name: 3-(4-methoxy-phenyl)-2-phenylimino-thiazolidin-4-one
• Synonyms: 3-(4-methoxy-phenyl)-2-phenylimino-thiazolidin-4-one
• CAS NO: 32826-80-5
• Molecular Weight: 298.365
• Mol File: 32826-80-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(4-methoxy-phenyl)-2-phenylimino-thiazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxy-phenyl)-2-phenylimino-thiazolidin-4-one(32826-80-5)
• EPA Substance Registry System: 3-(4-methoxy-phenyl)-2-phenylimino-thiazolidin-4-one(32826-80-5)

Safety Data

• Hazardous Substances Data: 32826-80-5(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 103-72-0 phenyl isothiocyanate 
• 1219-96-1 N¹-phenyl-N²-(p-methoxyphenyl)thiourea 
• 79-11-8 chloroacetic acid 
• 1219-96-1 N-(p-methoxyphenyl)-N'-phenylthiourea 

Downstream Products

• 114710-76-8 3-Allyl-2-[(Z)-phenylimino]-thiazolidin-4-one 
• 7341-63-1 N¹-phenyl-N²-allylthiourea 
• 32826-88-3 3-(4-methoxyphenyl)-1,3-thiazolidine-2,4-dione 
• 62-53-3 aniline 
• 36969-60-5 3-(4-methoxy-phenyl)-1,1-dioxo-2-phenylimino-1λ⁶-thiazolidin-4-one 

Relevant articles and documents

Synthesis of some 3,5-disubstituted phenyl-5,6-dihydrofuro[2,3-d]thiazol-2(3H)-ylidene) imines as potential pesticides

A new series of novel 3,5-disubstituted phenyl-5,6-dihydrofuro[2,3-d]thiazol-2(3H)-ylidene) imines have been synthesized from a common intermediate, in good yield. These compounds have been screened for their herbicidal activities against èchinochloa oryzicola, Echinochloa crus-galli, Oryza sativa, Glycine max and antifungal activities against Aspergillus Niger and Pyricularia oryzae whereas for antimicrobial activities, they have been screened against Salmonella typhi, Escherichia coli, Klebsiella pneumoniae, Bacillus subtilis and Bacillus pumilus.

Influence of Substituents on the Synthesis of Thiazolidinones

The influence of substituents (subunits) in the synthesis of thiazolidinones by the reaction of unsymmetrical thioureas with monochloroacetic acid in ethanol has been rationalised by the characterisation of the hydrolysis products of the resulting thiazolidinones.The formation of thiol from thiourea, which is the key intermediate in thiazolidinone synthesis, invariably involves the -NH- group adjacent to more electron withdrawing subunits.