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Prostaglandin E-2

Base Information
  • Chemical Name:Prostaglandin E-2
  • CAS No.:154170-57-7
  • Molecular Formula:C20H32 O5
  • Molecular Weight:352.471
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80274262
  • Mol file:154170-57-7.mol
Prostaglandin E-2

Synonyms:Prostaglandin E-2;DTXSID80274262;L024045;(5Z)-7-(3-Hydroxy-2-((1E)-3-hydroxy-1-octen-1-yl)-5-oxocyclopentyl)-5-heptenoic acid

Suppliers and Price of Prostaglandin E-2
Supply Marketing:
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
Total 16 raw suppliers
Chemical Property of Prostaglandin E-2
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:66-68℃ 
  • Boiling Point:530.071°C at 760 mmHg 
  • Flash Point:288.452°C 
  • PSA:94.83000 
  • LogP:3.25110 
  • Water Solubility.:insoluble 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:12
  • Exact Mass:352.22497412
  • Heavy Atom Count:25
  • Complexity:469
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s): R60:; R22:; 
  • Hazard Codes: T:Toxic;
     
  • Statements: R60:; R22:; 
  • Safety Statements: S53:; S22:; S26:; S36/37/39:; 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCC(C=CC1C(CC(=O)C1CC=CCCCC(=O)O)O)O
  • Isomeric SMILES:CCCCCC(/C=C/C1C(CC(=O)C1C/C=C\CCCC(=O)O)O)O
Technology Process of Prostaglandin E-2

There total 1 articles about Prostaglandin E-2 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:
aus entspr. Trichlorethylester;
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