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1-(Benzoylamino)methyl-3,4-dihydro isoquinoline

Base Information
  • Chemical Name:1-(Benzoylamino)methyl-3,4-dihydro isoquinoline
  • CAS No.:19382-36-6
  • Molecular Formula:C17H14N2O
  • Molecular Weight:262.311
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70563793
  • Wikidata:Q82448283
1-(Benzoylamino)methyl-3,4-dihydro isoquinoline

Synonyms:1-(BENZOYLAMINO)METHYL-3,4-DIHYDRO ISOQUINOLINE;132056-76-9;19382-36-6;1-(Benzoylamino)Methyl-3,4-Dihydro-Iso-Quinoline;N-(3,4-dihydroisoquinolin-1-ylmethyl)benzamide;N-[(3,4-Dihydroisoquinolin-1-yl)methyl]benzamide;DTXSID70563793;2-Amino-1-(4 inverted exclamation mark -chlorophenyl)propan-1-ol

Suppliers and Price of 1-(Benzoylamino)methyl-3,4-dihydro isoquinoline
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of 1-(Benzoylamino)methyl-3,4-dihydro isoquinoline
Chemical Property:
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:264.126263138
  • Heavy Atom Count:20
  • Complexity:371
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CN=C(C2=CC=CC=C21)CNC(=O)C3=CC=CC=C3
Technology Process of 1-(Benzoylamino)methyl-3,4-dihydro isoquinoline

There total 4 articles about 1-(Benzoylamino)methyl-3,4-dihydro isoquinoline 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:
With potassium carbonate; In ethanol; water; for 5h; Heating;
Guidance literature:
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 16h; Inert atmosphere;
DOI:10.1021/ol400870b
Guidance literature:
Multi-step reaction with 2 steps
1: hydrogen; palladium 10% on activated carbon / acetic acid / 6 h / 20 °C / 10343.2 Torr / Autoclave
2: triethylamine / dichloromethane / 16 h / 0 - 20 °C / Inert atmosphere
With palladium 10% on activated carbon; hydrogen; triethylamine; In dichloromethane; acetic acid;
DOI:10.1021/ol400870b
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