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3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI)

Base Information
  • Chemical Name:3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI)
  • CAS No.:145554-63-8
  • Molecular Formula:C9H12N2
  • Molecular Weight:148.208
  • Hs Code.:
  • Mol file:145554-63-8.mol
3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI)

Synonyms:3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI)

Suppliers and Price of 3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI)
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
  • AccelPharmtech
  • (R)-1,2,3,4-tetrahydro-3-Quinolinamine 97.00%
  • 25G
  • $ 12000.00
  • AccelPharmtech
  • (R)-1,2,3,4-tetrahydro-3-Quinolinamine 97.00%
  • 5G
  • $ 6320.00
  • AccelPharmtech
  • (R)-1,2,3,4-tetrahydro-3-Quinolinamine 97.00%
  • 1G
  • $ 3660.00
Total 1 raw suppliers
Chemical Property of 3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI)
Chemical Property:
Purity/Quality:

(R)-1,2,3,4-tetrahydro-3-Quinolinamine 97.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI)

There total 11 articles about 3-Quinolinamine,1,2,3,4-tetrahydro-,(R)-(9CI) 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:
3-aminoquinoline; With H2SiEt2; tris(pentafluorophenyl)borate; In chloroform; at 100 ℃; for 24h; Inert atmosphere;
With hydrogenchloride; In diethyl ether; at 20 ℃; for 1h;
DOI:10.1055/s-0036-1588442
Guidance literature:
Multi-step reaction with 4 steps
1: sodium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / water; dichloromethane / 24 h / 20 °C
2: bis-[(trifluoroacetoxy)iodo]benzene; trifluoroacetic acid / dichloromethane / 1.17 h / 0 °C
3: hydrogen; palladium 10% on activated carbon / ethanol / 2585.81 Torr
4: dimethyl sulfide borane / tetrahydrofuran / 120 h / 0 - 20 °C / Reflux
With palladium 10% on activated carbon; hydrogen; dimethyl sulfide borane; sodium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; bis-[(trifluoroacetoxy)iodo]benzene; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1021/acs.jmedchem.5b01612
Guidance literature:
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 40 ℃; for 2h;
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