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Spirapril

Base Information Edit
  • Chemical Name:Spirapril
  • CAS No.:83647-97-6
  • Molecular Formula:C22H30N2O5S2
  • Molecular Weight:466.623
  • Hs Code.:
  • UNII:96U2K78I3V
  • DSSTox Substance ID:DTXSID1044300
  • Nikkaji Number:J33.109K
  • Wikipedia:Spirapril
  • Wikidata:Q835757
  • NCI Thesaurus Code:C66560
  • Pharos Ligand ID:TX9FQNU8VNG6
  • Metabolomics Workbench ID:43510
  • ChEMBL ID:CHEMBL431
  • Mol file:83647-97-6.mol
Spirapril

Synonyms:Quadropril;Renormax;Renpress;SCH 33844;SCH-33844;spirapril;spirapril hydrochloride

Suppliers and Price of Spirapril
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
  • CSNpharm
  • Spirapril
  • 1g
  • $ 1200.00
  • Crysdot
  • Spirapril 95+%
  • 1g
  • $ 1191.00
  • Chemenu
  • (S)-7-(((S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl)-L-alanyl)-1,4-dithia-7-azaspiro[4.4]nonane-8-carboxylicacid 95%
  • 1g
  • $ 1122.00
  • American Custom Chemicals Corporation
  • SPIRAPRIL 95.00%
  • 1G
  • $ 1904.70
  • American Custom Chemicals Corporation
  • SPIRAPRIL 95.00%
  • 250MG
  • $ 697.34
  • American Custom Chemicals Corporation
  • SPIRAPRIL 95.00%
  • 100MG
  • $ 624.57
  • AHH
  • Spirapril 98%
  • 5g
  • $ 830.00
Total 32 raw suppliers
Chemical Property of Spirapril Edit
Chemical Property:
  • Vapor Pressure:1.93E-20mmHg at 25°C 
  • Refractive Index:1.621 
  • Boiling Point:697.8 °C at 760 mmHg 
  • Flash Point:375.8 °C 
  • PSA:146.54000 
  • Density:1.32 g/cm3 
  • LogP:2.71960 
  • Storage Temp.:2-8°C 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:10
  • Exact Mass:466.15961441
  • Heavy Atom Count:31
  • Complexity:650
Purity/Quality:

99% *data from raw suppliers

Spirapril *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2CC3(CC2C(=O)O)SCCS3
  • Isomeric SMILES:CCOC(=O)[C@H](CCC1=CC=CC=C1)N[C@@H](C)C(=O)N2CC3(C[C@H]2C(=O)O)SCCS3
Technology Process of Spirapril

There total 11 articles about Spirapril 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: 6.8 g / SOCl2 / 20 h / Heating
2: 3.86 g / p-toluenesulfonic acid / acetic acid / 44 h / Heating
3: 6.3 g / 20percent HBr/glacial acetic acid / 2 h / Ambient temperature
4: 3.64 g / 2.5 N aq. NaOH / methanol / 18 h / Ambient temperature
5: 1.) N,N-disuccinimidyl carbonate, pyridine, 2.) NEt3 / 1.) CH3CN, RT, 44 h, 2.) CH3CN, H2O, RT
With pyridine; sodium hydroxide; thionyl chloride; di(succinimido) carbonate; hydrogen bromide; toluene-4-sulfonic acid; acetic acid; triethylamine; In methanol; acetic acid;
DOI:10.1021/jm00127a033
Guidance literature:
Multi-step reaction with 2 steps
1: 1->3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / dimethylformamide / 18 h / Ambient temperature
2: 4.6 g / NEt3 / dimethylformamide / Ambient temperature
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide;
DOI:10.1021/jm00127a033
Guidance literature:
Multi-step reaction with 4 steps
1: 3.86 g / p-toluenesulfonic acid / acetic acid / 44 h / Heating
2: 6.3 g / 20percent HBr/glacial acetic acid / 2 h / Ambient temperature
3: 3.64 g / 2.5 N aq. NaOH / methanol / 18 h / Ambient temperature
4: 1.) N,N-disuccinimidyl carbonate, pyridine, 2.) NEt3 / 1.) CH3CN, RT, 44 h, 2.) CH3CN, H2O, RT
With pyridine; sodium hydroxide; di(succinimido) carbonate; hydrogen bromide; toluene-4-sulfonic acid; acetic acid; triethylamine; In methanol; acetic acid;
DOI:10.1021/jm00127a033
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