1-Methoxy-2-phenyl-1H-indole

Base Information

Chemical Name:1-Methoxy-2-phenyl-1H-indole
CAS No.:16616-82-3
Molecular Formula:C15H13 N O
Molecular Weight:223.274
Hs Code.:
European Community (EC) Number:240-664-0
DSSTox Substance ID:DTXSID4066090
Nikkaji Number:J318.260F
Wikidata:Q81992668
Mol file:16616-82-3.mol

Synonyms:1-Methoxy-2-phenylindole;1-Methoxy-2-phenyl-1H-indole;16616-82-3;1H-Indole, 1-methoxy-2-phenyl-;EINECS 240-664-0;DTXSID4066090;SCHEMBL11747741

Suppliers and Price of 1-Methoxy-2-phenyl-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 5 raw suppliers

Chemical Property of 1-Methoxy-2-phenyl-1H-indole

Chemical Property:

Vapor Pressure:6.12E-06mmHg at 25°C
Boiling Point:378.8°C at 760 mmHg
Flash Point:182.9°C
PSA：14.16000
Density:1.08g/cm³
LogP:3.36670
XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:223.099714038
Heavy Atom Count:17
Complexity:249

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CON1C2=CC=CC=C2C=C1C3=CC=CC=C3

Technology Process of 1-Methoxy-2-phenyl-1H-indole

There total 9 articles about 1-Methoxy-2-phenyl-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: 70.0%

: 108-86-1,52753-63-6
bromobenzene

: lithium triethyl(1-methoxyindol-2-yl)borate

: 16616-82-3
1-methoxy-2-phenylindole

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; at 60 ℃; for 3h;
DOI:10.1002/jhet.5570360408

Reference yield: 50.0%

: 54698-11-2
1-methoxyindole

: 1483-72-3
diphenyliodonium chloride

: 16616-82-3
1-methoxy-2-phenylindole

Guidance literature:: 1-methoxyindole; With tert.-butyl lithium; In tetrahydrofuran; pentane; at 20 ℃;

In tetrahydrofuran; pentane; at -20 ℃;

diphenyliodonium chloride; In tetrahydrofuran; pentane; at -20 - 20 ℃;
DOI:10.3987/COM-06-10865

Reference yield:

: 4264-29-3
(E)-2-nitrostilbene

: 16616-82-3
1-methoxy-2-phenylindole

Guidance literature:: Multi-step reaction with 2 steps

1: sodium t-butanolate / tetrahydrofuran / 40 h / 25 °C / Sealed tube; Inert atmosphere

2: tetrahydrofuran / 2 h / 25 °C / Inert atmosphere

With sodium t-butanolate; In tetrahydrofuran;
DOI:10.1002/anie.202104319