54397-16-9

Basic information

• Product Name: 4-Thiazolidinone, 3-(4-methylphenyl)-2-phenyl-
• CAS NO: 54397-16-9
• Molecular Formula: C16H15NOS
• Molecular Weight: 269.367
• Mol File: 54397-16-9.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: 4-Thiazolidinone, 3-(4-methylphenyl)-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Thiazolidinone, 3-(4-methylphenyl)-2-phenyl-(54397-16-9)
• EPA Substance Registry System: 4-Thiazolidinone, 3-(4-methylphenyl)-2-phenyl-(54397-16-9)

Safety Data

• Hazardous Substances Data: 54397-16-9(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 106-49-0 p-toluidine 
• 68-11-1 mercaptoacetic acid 
• 2272-45-9 benzal-p-toluidine 
• 2101-86-2 p-methylazidobenzene 

Downstream Products

• 10205-58-0 6-methyl-2-phenyl-1,3-benzothiazole 
• 613-33-2 (4,4'-dimethyl-1,1'-biphenyl) 
• 614-96-0 5-methyl-1H-indole 
• 122-00-9 para-methylacetophenone 
• 103-89-9 4-Methylacetanilide 
• 134-81-6 benzil 
• 130887-92-2 2-phenyl-3-(4-methylphenyl)-5-phenylmethylene-4-oxo-1,3-thiazolidine 
• 1353992-42-3 5-(4-dimethylaminobenzylidene)-2-phenyl-3-(4-methyphenyl)-4-thiazolidinone 
• 1353992-43-4 2-phenyl-5-(3-phenylallylidene)-3-(4-methyphenyl)-4-thiazolidinone 
• 1353992-40-1 5-(4-methoxybenzylidene)-2-phenyl-3-(4-methyphenyl)-4-thiazolidinone 
• 1353992-38-7 5-(4-chlorobenzylidene)-2-phenyl-3-(4-methyphenyl)-4-thiazolidinone 
• 130887-98-8 2-phenyl-3-(4-methylphenyl)-5-(α-phenylmethylaminobenzyl)-4-oxo-1,3-thiazolidine-1-oxide 
• 130888-00-5 2-phenyl-3-(4-methylphenyl)-5-(α-phenylmethylbenzyl)-4-oxo-1,3-thiazolidine-1-oxide 
• 130887-95-5 2-phenyl-3-(4-methylphenyl)-5-phenylmethylene-4-oxo-1,3-thiazolidine-1-oxide 

Relevant articles and documents

Condensation–cyclization reaction for one-pot synthesis of 1,3-thiazolidin-4-one derivatives by poly(p-phenylenediamine) grafted on LDHs as a catalyst with green tool

The three-component reaction between amine, carbonyl compound and thioglycolic acid is now considered as a major strategy for synthesis of 1,3-thiazolidin-4-ones, which consists of the following steps: (i) condensation of aldehyde and amine which results

Visible-light-driven photocatalytic activity of ZnO/g-C3N4 heterojunction for the green synthesis of biologically interest small molecules of thiazolidinones

Designing a photocatalytic system with complementary properties including high surface area, high loading, extraordinary electronic properties, and easy separation for increases photocatalytic performance has remained a challenge in photocatalytic applications. Herein, an environmentally benign approach was developed to fabricate graphitic carbon nitride (g-C3N4) decorated with nanorods zinc oxide (ZnO). The photocatalytic activity of ZnO decorated on the g-C3N4 surface was developed in the synthesis of 1,3-thiazolidin-4-ones and bis-thiazolidinones under very mild and sustainable reaction conditions. The reaction can be carried out by utilizing visible light without the requirement of any additive and other external sources of energy. It was found that the proposed photocatalyst is a more facile, recyclable, large-scale application and provides some new insights into the stabilization of semiconductors for a variety of applications.

TS-1 zeolite as a Lewis acid catalyst for solvent-free one-pot synthesis of 1,3-thiazolidin-4-ones

Abstract: Titanium silicate (TS-1) zeolite heterogeneous catalyst is synthesized by the hydrothermally discontinuous method and is characterized by using XRD, SEM, TEM, and NH3–TPD techniques. The catalytic activity of the TS-1 type zeolite was tested for one-pot solvent-free synthesis of 1,3-thiazolidine-4-ones. The present technique illustrates many benefits, including eco-friendly reaction conditions, environmentally helpful, short response time, simplicity, straightforward separatation, catalyst reusability and high yields of the products. Furthermore, the catalyst was utilized for four recycle reactions and it has been found that the catalyst shows consistent chemical process activity. Graphical abstract: [Figure not available: see fulltext.].