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4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester

Base Information Edit
  • Chemical Name:4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester
  • CAS No.:132089-40-8
  • Molecular Formula:C13H13NO2S
  • Molecular Weight:247.31300
  • Hs Code.:
  • Mol file:132089-40-8.mol
4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester

Synonyms:2-POhenyl-4-methyl-5-ethoxycarbonylthiazol;5-methyl-2-phenyl-thiazole-4-carboxylic acid ethyl ester;5-methyl-2-phenylthiazole-4-carboxylic acid ethyl ester;ethyl 5-methyl-2-phenyl-1,3-thiazole-4-carboxylate;

Suppliers and Price of 4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Matrix Scientific
  • 5-Methyl-2-phenylthiazole-4-carboxylic acid ethyl ester 95%+
  • 1g
  • $ 580.00
  • Labseeker
  • ethyl5-methyl-2-phenylthiazole-4-carboxylate 95
  • 10g
  • $ 3938.00
Total 8 raw suppliers
Chemical Property of 4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester Edit
Chemical Property:
  • Melting Point:80-81 °C(Solv: ethyl acetate (141-78-6); ligroine (8032-32-4)) 
  • Boiling Point:372.9±34.0 °C(Predicted) 
  • PSA:67.43000 
  • Density:1.188±0.06 g/cm3(Predicted) 
  • LogP:3.29520 
Purity/Quality:

99% *data from raw suppliers

5-Methyl-2-phenylthiazole-4-carboxylic acid ethyl ester 95%+ *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester

There total 4 articles about 4-Thiazolecarboxylic acid, 5-methyl-2-phenyl-, ethyl ester 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:
Multi-step reaction with 2 steps
1: 62 percent / Rh2(OAc)4 / 1,2-dichloro-ethane / Heating
2: 53 percent / Lawesson's reagent / tetrahydrofuran / Heating
With Lawessons reagent; dirhodium tetraacetate; In tetrahydrofuran; 1,2-dichloro-ethane;
DOI:10.1016/j.tet.2004.03.037
Guidance literature:
Multi-step reaction with 3 steps
1: 83 percent / 4-acetamidobenzenesulfonyl azide; triethylamine / acetonitrile / 16 h / 20 °C
2: 62 percent / Rh2(OAc)4 / 1,2-dichloro-ethane / Heating
3: 53 percent / Lawesson's reagent / tetrahydrofuran / Heating
With Lawessons reagent; 4-acetamidobenzenesulfonyl azide; triethylamine; dirhodium tetraacetate; In tetrahydrofuran; 1,2-dichloro-ethane; acetonitrile;
DOI:10.1016/j.tet.2004.03.037
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