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4-Methyl-1-propylquinolinium iodide

Base Information
  • Chemical Name:4-Methyl-1-propylquinolinium iodide
  • CAS No.:32863-55-1
  • Molecular Formula:C13H16 N . I
  • Molecular Weight:313.181
  • Hs Code.:2933499090
  • European Community (EC) Number:251-268-2
  • DSSTox Substance ID:DTXSID30885544
  • Mol file:32863-55-1.mol
4-Methyl-1-propylquinolinium iodide

Synonyms:4-Methyl-1-propylquinolinium iodide;32863-55-1;1-Propyllepidinium iodide;Quinolinium, 4-methyl-1-propyl-, iodide (1:1);EINECS 251-268-2;Quinolinium, 4-methyl-1-propyl-, iodide;4-methyl-1-propylquinolin-1-ium iodide;DTXSID30885544;EN300-9399114;Z1486012676

Suppliers and Price of 4-Methyl-1-propylquinolinium iodide
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
  • American Custom Chemicals Corporation
  • 4-METHYL-1-PROPYLQUINOLINIUM IODIDE 95.00%
  • 5MG
  • $ 502.32
Total 5 raw suppliers
Chemical Property of 4-Methyl-1-propylquinolinium iodide
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:3.88000 
  • Density:g/cm3 
  • LogP:-0.15030 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:313.03275
  • Heavy Atom Count:15
  • Complexity:178
Purity/Quality:

99% *data from raw suppliers

4-METHYL-1-PROPYLQUINOLINIUM IODIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC[N+]1=CC=C(C2=CC=CC=C21)C.[I-]
Technology Process of 4-Methyl-1-propylquinolinium iodide

There total 3 articles about 4-Methyl-1-propylquinolinium iodide 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:
at 130 ℃; for 0.0833333h; Microwave irradiation;
DOI:10.3390/molecules181114306
Guidance literature:
Multi-step reaction with 3 steps
1.1: neat (no solvent) / 180 °C / Inert atmosphere
1.2: 3 h / 95 °C / Acidic conditions; Inert atmosphere
2.1: trichlorophosphate / Reflux; Inert atmosphere
2.2: Inert atmosphere
3.1: methanol / 80 °C / Sealed tube; Inert atmosphere
With trichlorophosphate; In methanol;
DOI:10.1016/j.bmcl.2019.126725
Guidance literature:
Multi-step reaction with 2 steps
1.1: trichlorophosphate / Reflux; Inert atmosphere
1.2: Inert atmosphere
2.1: methanol / 80 °C / Sealed tube; Inert atmosphere
With trichlorophosphate; In methanol;
DOI:10.1016/j.bmcl.2019.126725
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