1-methyl-2-(1-phenylvinyl)-1H-indole

Base Information

Chemical Name:1-methyl-2-(1-phenylvinyl)-1H-indole
CAS No.:66643-64-9
Molecular Formula:C17H15N
Molecular Weight:233.313
Hs Code.:
DSSTox Substance ID:DTXSID80496624
Nikkaji Number:J277.599I
Wikidata:Q82345605

Synonyms:1-methyl-2-(1-phenylvinyl)-1H-indole;66643-64-9;DTXSID80496624;1-methyl-2-(1-phenyl-vinyl)-1H-indole;1-Methyl-2-(1-phenylethenyl)-1H-indole

Suppliers and Price of 1-methyl-2-(1-phenylvinyl)-1H-indole

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 1 raw suppliers

Chemical Property of 1-methyl-2-(1-phenylvinyl)-1H-indole

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:2
Exact Mass:233.120449483
Heavy Atom Count:18
Complexity:303

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=CC=CC=C2C=C1C(=C)C3=CC=CC=C3

Technology Process of 1-methyl-2-(1-phenylvinyl)-1H-indole

There total 5 articles about 1-methyl-2-(1-phenylvinyl)-1H-indole 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: 77.0%

: 1029-43-2
1-(1-methyl-2-indolyl)-1-phenylethanol

: 66643-64-9
1-phenyl-1-(2-N-methylindolyl)ethylene

Guidance literature:: With trifluoroacetic acid; In chloroform; at 20 ℃; for 0.0333333h;
DOI:10.1016/S0040-4020(01)91317-1

Reference yield:

: 603-76-9
1-methylindole

: 66643-64-9
1-phenyl-1-(2-N-methylindolyl)ethylene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) ether, hexane, then 6 h, reflux, 2.) ether, hexane, 20 deg C, then 2h, reflux, and 12 h, 20 deg C

2: 77 percent / CF₃COOH / CHCl₃ / 0.03 h / 20 °C

With n-butyllithium; trifluoroacetic acid; In chloroform;
DOI:10.1016/S0040-4020(01)91317-1

Reference yield:

: 98-86-2
acetophenone

: 66643-64-9
1-phenyl-1-(2-N-methylindolyl)ethylene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) ether, hexane, then 6 h, reflux, 2.) ether, hexane, 20 deg C, then 2h, reflux, and 12 h, 20 deg C

2: 77 percent / CF₃COOH / CHCl₃ / 0.03 h / 20 °C

With n-butyllithium; trifluoroacetic acid; In chloroform;
DOI:10.1016/S0040-4020(01)91317-1