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Ceronapril

Base Information Edit
  • Chemical Name:Ceronapril
  • CAS No.:111223-26-8
  • Molecular Formula:C21H33 N2 O6 P
  • Molecular Weight:440.477
  • Hs Code.:
  • UNII:X3MM60SOVP
  • DSSTox Substance ID:DTXSID80891418
  • Nikkaji Number:J304.212J
  • Wikipedia:Ceronapril
  • Wikidata:Q27293516
  • NCI Thesaurus Code:C169841
  • Pharos Ligand ID:MRTU35Q15QUN
  • ChEMBL ID:CHEMBL36503
  • Mol file:111223-26-8.mol
Ceronapril

Synonyms:1-(6-amino-2-((hydroxy(4-phenylbutyl)phosphinyl)oxy)-1-oxohexyl)proline;ceranapril;ceronapril;SQ 29852;SQ-29,852

Suppliers and Price of Ceronapril
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
  • CERONAPRIL 95.00%
  • 5MG
  • $ 501.85
Total 1 raw suppliers
Chemical Property of Ceronapril Edit
Chemical Property:
  • Vapor Pressure:1.4E-19mmHg at 25°C 
  • Melting Point:190-195° (dec) 
  • Boiling Point:682.8°C at 760 mmHg 
  • Flash Point:366.7°C 
  • PSA:139.97000 
  • Density:1.265g/cm3 
  • LogP:3.42270 
  • XLogP3:-0.7
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:13
  • Exact Mass:440.20762377
  • Heavy Atom Count:30
  • Complexity:596
Purity/Quality:

99.0%min *data from raw suppliers

CERONAPRIL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC(N(C1)C(=O)C(CCCCN)OP(=O)(CCCCC2=CC=CC=C2)O)C(=O)O
  • Isomeric SMILES:C1C[C@H](N(C1)C(=O)[C@H](CCCCN)OP(=O)(CCCCC2=CC=CC=C2)O)C(=O)O
  • Uses Antihypertensive.
Technology Process of Ceronapril

There total 15 articles about Ceronapril 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:
With hydrogen; palladium dihydroxide; In methanol; for 3h;
DOI:10.1021/jm00396a033
Guidance literature:
Multi-step reaction with 4 steps
1: sodium hypophosphite hydrate, H2SO4, AIBN / ethanol / 22 h / Heating
2: DCC, DMAP / tetrahydrofuran / 2 h / Ambient temperature
3: NaIO4 / dioxane; H2O / 16 h
4: 78 percent / H2 / Pd(OH)2/C / methanol / 3 h
With dmap; sodium periodate; sodium hypophosphite; 2,2'-azobis(isobutyronitrile); sulfuric acid; hydrogen; dicyclohexyl-carbodiimide; palladium dihydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; water;
DOI:10.1021/jm00396a033
Guidance literature:
Multi-step reaction with 5 steps
1: 94 percent / aq. NaOH / 45 h / 0 °C / pH 10
2: 94 percent / Et3N, hydroxybenzotriazole, DCC / tetrahydrofuran / 1.) 0 deg C. 3 h, 2.) room temperature, 1 h
3: DCC, DMAP / tetrahydrofuran / 2 h / Ambient temperature
4: NaIO4 / dioxane; H2O / 16 h
5: 78 percent / H2 / Pd(OH)2/C / methanol / 3 h
With dmap; sodium hydroxide; sodium periodate; hydrogen; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium dihydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; water;
DOI:10.1021/jm00396a033
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