3-(3-Chlorophenyl)-2-phenyl-1,3-thiazolidin-4-one

Base Information

• Chemical Name: 3-(3-Chlorophenyl)-2-phenyl-1,3-thiazolidin-4-one
• CAS No.: 117664-55-8
• Molecular Formula: C₁₅H₁₂ClNOS
• Molecular Weight: 289.785
• DSSTox Substance ID: DTXSID30385817
• Nikkaji Number: J752.267C
• Mol file: 117664-55-8.mol

Synonyms:3-(3-chlorophenyl)-2-phenyl-1,3-thiazolidin-4-one;117664-55-8;4-Thiazolidinone, 3-(3-chlorophenyl)-2-phenyl-;DTXSID30385817;AKOS001484241;PK04_181174;2-Phenyl-3-(3-chlorophenyl)thiazolidin-4-one;AB00084049-01;SR-01000422632;SR-01000422632-1;BRD-A98951712-001-01-1

Chemical Property of 3-(3-Chlorophenyl)-2-phenyl-1,3-thiazolidin-4-one

Chemical Property:

• XLogP3: 4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 289.0328129
• Heavy Atom Count: 19
• Complexity: 332

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(=O)N(C(S1)C2=CC=CC=C2)C3=CC(=CC=C3)Cl

Technology Process of 3-(3-Chlorophenyl)-2-phenyl-1,3-thiazolidin-4-one

There total 3 articles about 3-(3-Chlorophenyl)-2-phenyl-1,3-thiazolidin-4-one 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: 53.0%

N-(3-chlorobenzylidene)aniline (7519-65-5,32213-65-3) + mercaptoacetic acid (68-11-1) → 2-phenyl-3-(3-chlorophenyl)thiazolidin-4-one (117664-55-8)

Guidance literature:

In toluene; Heating;

Reference yield:

[(3-Chloro-phenylamino)-phenyl-methylsulfanyl]-acetic acid (126079-78-5) → 2-phenyl-3-(3-chlorophenyl)thiazolidin-4-one (117664-55-8)

Guidance literature:

In tetrachloromethane; at 76 ℃; Kinetics; other temperature, other solvent;

Reference yield:

→ 2-phenyl-3-(3-chlorophenyl)thiazolidin-4-one (117664-55-8)

Guidance literature:

/BRN= 236097/;

DOI:10.1021/ja01574a036

upstream raw materials:

N-(3-chlorobenzylidene)aniline

mercaptoacetic acid

[(3-Chloro-phenylamino)-phenyl-methylsulfanyl]-acetic acid

Downstream raw materials:

5-Bromo-3-(3-chloro-phenyl)-2-phenyl-thiazolidin-4-one

4-(3-Chloro-phenyl)-3-(4-fluoro-phenyl)-5-phenyl-4,5-dihydro-3H-thiazolo[4,5-d]thiazole-2-thione

(4-Fluoro-phenyl)-dithiocarbamic acid 3-(3-chloro-phenyl)-4-oxo-2-phenyl-thiazolidin-5-yl ester

[6-(3-Chloro-phenyl)-5-phenyl-5,6-dihydro-1-oxa-3,4-dithia-6-aza-pentalen-(2E)-ylidene]-(4-fluoro-phenyl)-amine