(1-Methylisoquinolin-2(1H)-yl)(phenyl)methanone

Base Information

Chemical Name:(1-Methylisoquinolin-2(1H)-yl)(phenyl)methanone
CAS No.:61456-83-5
Molecular Formula:C17H15NO
Molecular Weight:249.312
Hs Code.:
DSSTox Substance ID:DTXSID70560025
Nikkaji Number:J432.321A

Synonyms:61456-83-5;(1-Methylisoquinolin-2(1H)-yl)(phenyl)methanone;isoquinoline,2-benzoyl-1,2-dihydro-1-methyl-;DTXSID70560025

Suppliers and Price of (1-Methylisoquinolin-2(1H)-yl)(phenyl)methanone

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

Total 3 raw suppliers

Chemical Property of (1-Methylisoquinolin-2(1H)-yl)(phenyl)methanone

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:249.115364102
Heavy Atom Count:19
Complexity:356

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C2=CC=CC=C2C=CN1C(=O)C3=CC=CC=C3

Technology Process of (1-Methylisoquinolin-2(1H)-yl)(phenyl)methanone

There total 6 articles about (1-Methylisoquinolin-2(1H)-yl)(phenyl)methanone 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:

Reference yield: 50.0%

: 917-64-6
methyl magnesium iodide

: 138528-82-2
N-benzoylisoquinolinium triflate

: 61456-83-5
N-benzoyl-1-methyl-1,2-dihydroisoquinoline

Guidance literature:: In diethyl ether; at 0 ℃; for 1h;

Reference yield:

: 61206-56-2
N-benzoylisoquinolinium chloride

: 61456-83-5
N-benzoyl-1-methyl-1,2-dihydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 43 percent / CH₂Cl₂ / 24 h

2: 50 percent / diethyl ether / 1 h / 0 °C

In diethyl ether; dichloromethane;

Reference yield:

: 138528-82-2
N-benzoylisoquinolinium triflate

: 61456-83-5
N-benzoyl-1-methyl-1,2-dihydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / sodium hydroxide / H₂O / 24 h

2: diethyl ether / 0 °C

With sodium hydroxide; In diethyl ether; water;