4-Thiazolidinone, 5-[(4-methoxyphenyl)methylene]-3-methyl-2-thioxo-

Base Information

• Chemical Name: 4-Thiazolidinone, 5-[(4-methoxyphenyl)methylene]-3-methyl-2-thioxo-
• CAS No.: 28996-49-8
• Molecular Formula: C12H11NO2S2
• Molecular Weight: 265.357
• DSSTox Substance ID: DTXSID40362058
• Mol file: 28996-49-8.mol

Synonyms:28996-49-8;4-Thiazolidinone, 5-[(4-methoxyphenyl)methylene]-3-methyl-2-thioxo-;ChemDiv3_000488;DTXSID40362058

Chemical Property of 4-Thiazolidinone, 5-[(4-methoxyphenyl)methylene]-3-methyl-2-thioxo-

Chemical Property:

• Boiling Point: 410.9±55.0 °C(Predicted)
• PSA: 86.93000
• Density: 1.38±0.1 g/cm3(Predicted)
• LogP: 2.46410
• XLogP3: 2.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 265.02312094
• Heavy Atom Count: 17
• Complexity: 360

Purity/Quality:

5-(4-METHOXYBENZYLIDENE)-3-METHYL-2-THIOXO-1,3-THIAZOLIDIN-4-ONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1C(=O)C(=CC2=CC=C(C=C2)OC)SC1=S

Technology Process of 4-Thiazolidinone, 5-[(4-methoxyphenyl)methylene]-3-methyl-2-thioxo-

There total 6 articles about 4-Thiazolidinone, 5-[(4-methoxyphenyl)methylene]-3-methyl-2-thioxo- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 78.0%

3-Methyl-2-thioxo-thiazolidin-4-on (4807-55-0) + 4-methoxy-benzaldehyde (123-11-5) → 5-(4-methoxyphenylmethylene)-3-methyl-4-oxo-2-thioxothiazolidine (28996-49-8)

Guidance literature:

With aluminum oxide; potassium fluoride; In solid; for 0.0666667h; microwaves (350 W);

Reference yield: 10.0%

5-(4-methoxybenzylidene)-2-thioxo-4-thiazolidinone (5462-97-5,81154-16-7) + dimethyl sulfate (77-78-1) → 5-(4-methoxy-benzylidene)-2-methylsulfanyl-thiazol-4-one (28996-11-4) + 5-(4-methoxyphenylmethylene)-3-methyl-4-oxo-2-thioxothiazolidine (28996-49-8)

Guidance literature:

With potassium carbonate; In acetone; for 20h; Heating;

Reference yield:

4-methoxy-benzaldehyde (123-11-5) → 5-(4-methoxyphenylmethylene)-3-methyl-4-oxo-2-thioxothiazolidine (28996-49-8)

Guidance literature:

With acetic acid;

upstream raw materials:

4-methoxy-benzaldehyde

thiocyanatoacetic acid, Na-salt

methyl thioisocyanate

diazomethane

Downstream raw materials:

5-(4-Methoxyphenylmethylene)-2-(phenylmethylimino)-3-methyl-4-thiazolidinone