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5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione

Base Information
  • Chemical Name:5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione
  • CAS No.:79525-07-8
  • Molecular Formula:C12H13NO4S
  • Molecular Weight:267.306
  • Hs Code.:
  • DSSTox Substance ID:DTXSID201000572
  • ChEMBL ID:CHEMBL4104501
5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione

Synonyms:BRN 5558540;79525-07-8;CHEMBL4104501;5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione;2,4-Thiazolidinedione, 5-((2,4-dimethoxyphenyl)methyl)-;SCHEMBL11158115;DTXSID201000572;BDBM50240910;LS-151317;5-[(2,4-Dimethoxyphenyl)methyl]-4-hydroxy-1,3-thiazol-2(5H)-one

Suppliers and Price of 5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
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Total 0 raw suppliers
Chemical Property of 5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione
Chemical Property:
  • Vapor Pressure:1.61E-08mmHg at 25°C 
  • Boiling Point:456.5°Cat760mmHg 
  • Flash Point:229.9°C 
  • Density:1.313g/cm3 
  • XLogP3:2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:267.05652907
  • Heavy Atom Count:18
  • Complexity:336
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC(=C(C=C1)CC2C(=O)NC(=O)S2)OC
Technology Process of 5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione

There total 5 articles about 5-((2,4-Dimethoxyphenyl)methyl)-2,4-thiazolidinedione 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:
Guidance literature:
With pyridine; lithium borohydride; In tetrahydrofuran; regiospecific reaction; Inert atmosphere; Reflux;
DOI:10.1021/acs.jmedchem.7b00606
Guidance literature:
Multi-step reaction with 4 steps
1: 92.9 percent / piperidine, benzoic acid / toluene / 4 h / Heating
2: H2 / 10percent Pd-C / methanol / 760 Torr / Ambient temperature
3: 74.2 percent / 60percent NaH, NCS / tetrahydrofuran / 0.5 h / Ambient temperature
With piperidine; N-chloro-succinimide; hydrogen; sodium hydride; benzoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; toluene;
DOI:10.1248/cpb.31.560
Guidance literature:
Multi-step reaction with 3 steps
1: H2 / 10percent Pd-C / methanol / 760 Torr / Ambient temperature
2: 74.2 percent / 60percent NaH, NCS / tetrahydrofuran / 0.5 h / Ambient temperature
With N-chloro-succinimide; hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1248/cpb.31.560
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