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3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(3-((((3-(4-(3-methoxyphenyl)-1-piperidinyl)propyl)amino)carbonyl)amino)phenyl)-2,6-dimethyl-, 3,5-dimethyl ester

Base Information
  • Chemical Name:3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(3-((((3-(4-(3-methoxyphenyl)-1-piperidinyl)propyl)amino)carbonyl)amino)phenyl)-2,6-dimethyl-, 3,5-dimethyl ester
  • CAS No.:186185-03-5
  • Molecular Formula:C33H42N4O6
  • Molecular Weight:590.72
  • Hs Code.:
  • European Community (EC) Number:663-935-9
  • UNII:819SRG2Y6N
  • DSSTox Substance ID:DTXSID501018102
  • Nikkaji Number:J1.692.874G
  • Wikidata:Q27269229
  • Pharos Ligand ID:PAJVW5D787CQ
  • ChEMBL ID:CHEMBL324554
  • Mol file:186185-03-5.mol
3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(3-((((3-(4-(3-methoxyphenyl)-1-piperidinyl)propyl)amino)carbonyl)amino)phenyl)-2,6-dimethyl-, 3,5-dimethyl ester

Synonyms:BMS 193885;BMS-193885;BMS193885

Suppliers and Price of 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(3-((((3-(4-(3-methoxyphenyl)-1-piperidinyl)propyl)amino)carbonyl)amino)phenyl)-2,6-dimethyl-, 3,5-dimethyl ester
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
  • BMS 193885
  • 10mg
  • $ 531.00
  • Tocris
  • BMS193885 ≥99%(HPLC)
  • 50
  • $ 1088.00
  • Tocris
  • BMS193885 ≥99%(HPLC)
  • 10
  • $ 271.00
  • Sigma-Aldrich
  • BMS-193885 ≥98% (HPLC)
  • 5mg
  • $ 138.00
  • Sigma-Aldrich
  • BMS-193885 ≥98% (HPLC)
  • 25mg
  • $ 550.00
  • American Custom Chemicals Corporation
  • BMS-193885 95.00%
  • 50MG
  • $ 1478.35
  • American Custom Chemicals Corporation
  • BMS-193885 95.00%
  • 10MG
  • $ 757.97
Total 5 raw suppliers
Chemical Property of 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(3-((((3-(4-(3-methoxyphenyl)-1-piperidinyl)propyl)amino)carbonyl)amino)phenyl)-2,6-dimethyl-, 3,5-dimethyl ester
Chemical Property:
  • Boiling Point:707.5±60.0 °C(Predicted) 
  • PKA:13.94±0.46(Predicted) 
  • PSA:121.72000 
  • Density:1.188±0.06 g/cm3(Predicted) 
  • LogP:5.21130 
  • Storage Temp.:Desiccate at +4°C 
  • Solubility.:DMSO: >10mg/mL 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:12
  • Exact Mass:590.31043507
  • Heavy Atom Count:43
  • Complexity:1010
Purity/Quality:

>98% *data from raw suppliers

BMS 193885 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C(C(=C(N1)C)C(=O)OC)C2=CC(=CC=C2)NC(=O)NCCCN3CCC(CC3)C4=CC(=CC=C4)OC)C(=O)OC
  • Uses BMS 193885, is a potent, and competitive neuropeptide (NPY) Y1 antagonist, that has also displayed 160-fold selectivity over σ1, α1, Y2, Y4 and Y5 receptors respectively. BMS 193885, is also brain penetrant, and able to reduce food intake and body weight through central Y1 inhibition.
Technology Process of 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(3-((((3-(4-(3-methoxyphenyl)-1-piperidinyl)propyl)amino)carbonyl)amino)phenyl)-2,6-dimethyl-, 3,5-dimethyl ester

There total 6 articles about 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-4-(3-((((3-(4-(3-methoxyphenyl)-1-piperidinyl)propyl)amino)carbonyl)amino)phenyl)-2,6-dimethyl-, 3,5-dimethyl ester 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 2 steps
1: NH3; H2; Raney Ni / H2O; methanol / 1 h / 2585.74 Torr
2: CH2Cl2 / 1 h
With ammonia; hydrogen; nickel; In methanol; dichloromethane; water;
DOI:10.1016/j.bmc.2003.10.016
Guidance literature:
Multi-step reaction with 3 steps
1: 96 percent / acetonitrile / 4 h / Heating
2: NH3; H2; Raney Ni / H2O; methanol / 1 h / 2585.74 Torr
3: CH2Cl2 / 1 h
With ammonia; hydrogen; nickel; In methanol; dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmc.2003.10.016
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