2-phenyl-1H-benzo[g]indole

Base Information

Chemical Name:2-phenyl-1H-benzo[g]indole
CAS No.:33555-17-8
Molecular Formula:C18H13N
Molecular Weight:243.308
Hs Code.:
DSSTox Substance ID:DTXSID20385301
Nikkaji Number:J1.218.260K

Synonyms:2-phenyl-1H-benzo[g]indole;33555-17-8;phenylbenz[g]indole;Oprea1_314845;SCHEMBL4891254;DTXSID20385301;ALIHHRJMNTXXJT-UHFFFAOYSA-N

Suppliers and Price of 2-phenyl-1H-benzo[g]indole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-phenyl-1H-benzo[g]indole

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:243.104799419
Heavy Atom Count:19
Complexity:307

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC3=C(N2)C4=CC=CC=C4C=C3

Technology Process of 2-phenyl-1H-benzo[g]indole

There total 38 articles about 2-phenyl-1H-benzo[g]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: 98.0%

: C₁₈H₁₃NO₂

: 33555-17-8
2-phenyl-1H-benzo[g]indole

Guidance literature:: With 4,7-dimethoxy-1,10-phenanthroline; phenylsilane; iron(II) acetate; In 1,2-dimethoxyethane; at 80 ℃;
DOI:10.1021/acscatal.7b01915

Reference yield: 95.0%

: 90-14-2
1-Iodonaphthalene

: 7654-06-0
3-phenyl-2H-azirine

: 33555-17-8
2-phenyl-1H-benzo[g]indole

Guidance literature:: With norborn-2-ene; tri(m-chlorophenyl)-phosphine; palladium diacetate; caesium carbonate; In acetonitrile; at 110 ℃; for 16h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/ol100975b

Reference yield: 94.0%

: 90-14-2
1-Iodonaphthalene

: 19433-17-1
acetophenone O-acetyloxime

: 33555-17-8
2-phenyl-1H-benzo[g]indole

Guidance literature:: With norborn-2-ene; trifuran-2-yl-phosphane; palladium diacetate; potassium carbonate; In 1,4-dioxane; dimethyl sulfoxide; at 80 ℃; for 24h; Inert atmosphere;