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Levamlodipine nicotinate

Base Information Edit
  • Chemical Name:Levamlodipine nicotinate
  • CAS No.:675605-61-5
  • Molecular Formula:C6H5NO2*C20H25ClN2O5
  • Molecular Weight:531.993
  • Hs Code.:
  • UNII:7EQG8Y8AHW
  • Mol file:675605-61-5.mol
Levamlodipine nicotinate

Synonyms:Levamlodipine nicotinate;7EQG8Y8AHW;(-)-AMLODIPINE NICOTINATE;3,5-Pyridinedicarboxylic acid, 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, (4S)-, 3-pyridinecarboxylate (1:1);3,5-Pyridinedicarboxylic acid, 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, (4S)-, mono-3-pyridinecarboxylate;675605-61-5;UNII-7EQG8Y8AHW;(s)-amlodipine nicotinate;SCHEMBL2255627;S Amlodipine Nicotinate [WHO-DD]

Suppliers and Price of Levamlodipine nicotinate
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
Total 0 raw suppliers
Chemical Property of Levamlodipine nicotinate Edit
Chemical Property:
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:11
  • Exact Mass:531.1772280
  • Heavy Atom Count:37
  • Complexity:760
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC(=O)C1=C(NC(=C(C1C2=CC=CC=C2Cl)C(=O)OC)C)COCCN.C1=CC(=CN=C1)C(=O)O
  • Isomeric SMILES:CCOC(=O)C1=C(NC(=C([C@@H]1C2=CC=CC=C2Cl)C(=O)OC)C)COCCN.C1=CC(=CN=C1)C(=O)O
Technology Process of Levamlodipine nicotinate

There total 1 articles about Levamlodipine nicotinate 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 Petroleum ether; for 5h; Heating / reflux;
upstream raw materials:

nicotinic acid

amlodipine

Refernces Edit
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