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Prednisolone 21-Ethylcarbonate

Base Information
  • Chemical Name:Prednisolone 21-Ethylcarbonate
  • CAS No.:2205-88-1
  • Molecular Formula:C24H32O7
  • Molecular Weight:432.514
  • Hs Code.:
  • UNII:2AZW35L4BF
  • Mol file:2205-88-1.mol
Prednisolone 21-Ethylcarbonate

Synonyms:P21EC cpd;prednisolone 21-ethylcarbonate

Suppliers and Price of Prednisolone 21-Ethylcarbonate
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
  • Usbiological
  • Prednisolone 21-Ethylcarbonate
  • 250mg
  • $ 460.00
  • TRC
  • Prednisolone21-Ethylcarbonate
  • 250mg
  • $ 185.00
  • TRC
  • Prednisolone21-Ethylcarbonate
  • 2.5g
  • $ 1455.00
  • Medical Isotopes, Inc.
  • Prednisolone21-Ethylcarbonate
  • 2.5 g
  • $ 2200.00
Total 8 raw suppliers
Chemical Property of Prednisolone 21-Ethylcarbonate
Chemical Property:
  • PSA:110.13000 
  • LogP:2.73840 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:6
  • Exact Mass:432.21480336
  • Heavy Atom Count:31
  • Complexity:860
Purity/Quality:

95+%HPLC *data from raw suppliers

Prednisolone 21-Ethylcarbonate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)C=CC34C)O)C)O
  • Isomeric SMILES:CCOC(=O)OCC(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@@H]([C@H]3[C@H]2CCC4=CC(=O)C=C[C@]34C)O)C)O
  • Uses Prednisolone 21-Ethylcarbonate is a derivative of Prednisolone (P703740), synthetic corticosteroid; metabolically interconvertible with prednisone.
Technology Process of Prednisolone 21-Ethylcarbonate

There total 4 articles about Prednisolone 21-Ethylcarbonate 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:
In acetone; for 0.5h; Heating;
DOI:10.1002/ardp.19863191016
Guidance literature:
With pyridine; at 22 ℃; for 2h;
Guidance literature:
With water; acetic acid; at 18 ℃; for 5h; Yield given. Yields of byproduct given;
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