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Dimethyl oxazole-4,5-dicarboxy

Base Information Edit
  • Chemical Name:Dimethyl oxazole-4,5-dicarboxy
  • CAS No.:72030-81-0
  • Molecular Formula:C7H7NO5
  • Molecular Weight:185.136
  • Hs Code.:
  • Mol file:72030-81-0.mol
Dimethyl oxazole-4,5-dicarboxy

Synonyms:dimethyl oxazole-4,5-dicarboxylate

Suppliers and Price of Dimethyl oxazole-4,5-dicarboxy
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
  • American Custom Chemicals Corporation
  • DIMETHYL OXAZOLE-4,5-DICARBOXYLATE 95.00%
  • 5MG
  • $ 504.57
  • Alfa Aesar
  • Dimethyl oxazole-4,5-dicarboxylate, 99%
  • 10g
  • $ 354.00
  • Alfa Aesar
  • Dimethyl oxazole-4,5-dicarboxylate, 99%
  • 1g
  • $ 57.10
Total 3 raw suppliers
Chemical Property of Dimethyl oxazole-4,5-dicarboxy Edit
Chemical Property:
  • Melting Point:74-76℃ 
  • Boiling Point:150℃/12mm 
Purity/Quality:

99% *data from raw suppliers

DIMETHYL OXAZOLE-4,5-DICARBOXYLATE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses The teroxazole has been synthesized from dimethyl oxazole-4,5-dicarboxylate and lithiobenzyl isocyanide.
Technology Process of Dimethyl oxazole-4,5-dicarboxy

There total 3 articles about Dimethyl oxazole-4,5-dicarboxy 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:
Multistep reaction; (i) imidazole, Et3N, THF, (ii) /BRN= 3537963/;
Guidance literature:
Dihydromaleinsaeuredimethylester, Formamid;
DOI:10.1002/oms.1210111005
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