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Prostaglandin D2 1,15-lactone

Base Information
  • Chemical Name:Prostaglandin D2 1,15-lactone
  • CAS No.:62410-98-4
  • Molecular Formula:C20H30O4
  • Molecular Weight:334.45
  • Hs Code.:
Prostaglandin D2 1,15-lactone

Synonyms:Prostaglandin D2 1,15-lactone;PGD2 1,15-lactone;BRN 5600045;Prosta-5,13-dien-1-oic acid, 9,15-dihydroxy-11-oxo-, lambda-lactone, (5Z,9-alpha,13E,15S)-;62410-98-4;LS-125824

Suppliers and Price of Prostaglandin D2 1,15-lactone
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 2 raw suppliers
Chemical Property of Prostaglandin D2 1,15-lactone
Chemical Property:
  • Vapor Pressure:4.53E-13mmHg at 25°C 
  • Boiling Point:521.8°C at 760 mmHg 
  • PKA:13.74±0.40(Predicted) 
  • Flash Point:180.9°C 
  • PSA:63.60000 
  • Density:1.046g/cm3 
  • LogP:3.73100 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:334.21440943
  • Heavy Atom Count:24
  • Complexity:480
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCC1C=CC2C(CC=CCCCC(=O)O1)C(CC2=O)O
  • Isomeric SMILES:CCCCC[C@H]1/C=C/[C@@H]2[C@@H](C/C=C\CCCC(=O)O1)[C@H](CC2=O)O
Technology Process of Prostaglandin D2 1,15-lactone

There total 5 articles about Prostaglandin D2 1,15-lactone 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 5 steps
1: 82 percent / imidazole / dimethylformamide / 1 h / 0 °C
2: 92 percent / pyridine hydrochloride / CH2Cl2 / 18 h / 25 °C
3: tetrabutylammonium fluoride / tetrahydrofuran / 0.5 h / 25 °C
4: H2CrO4, H2SO4 / acetone / 1.25 h / -30 - -20 °C
5: 243 mg / AcOH / H2O; tetrahydrofuran / 3 h / 40 °C
With 1H-imidazole; sulfuric acid; tetrabutyl ammonium fluoride; pyridine hydrochloride; chromic acid; acetic acid; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm00360a003
Guidance literature:
Multi-step reaction with 2 steps
1: H2CrO4, H2SO4 / acetone / 1.25 h / -30 - -20 °C
2: 243 mg / AcOH / H2O; tetrahydrofuran / 3 h / 40 °C
With sulfuric acid; chromic acid; acetic acid; In tetrahydrofuran; water; acetone;
DOI:10.1021/jm00360a003
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