N,1-dimethyl-N-phenylindole-2-carboxamide

Base Information

Chemical Name:N,1-dimethyl-N-phenylindole-2-carboxamide
CAS No.:62048-33-3
Molecular Formula:C17H16N2O
Molecular Weight:264.327
Hs Code.:
DSSTox Substance ID:DTXSID80393528
Nikkaji Number:J1.132.201H
Wikidata:Q82192325
ChEMBL ID:CHEMBL464798

Synonyms:CHEMBL464798;N,1-dimethyl-N-phenylindole-2-carboxamide;62048-33-3;N,1-Dimethyl-N-phenyl-1H-indole-2-carboxamide;DTXSID80393528;BDBM50273488;N-Methyl, N-phenyl-1-methyl-1H-indole-2-carboxamide

Suppliers and Price of N,1-dimethyl-N-phenylindole-2-carboxamide

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 0 raw suppliers

Chemical Property of N,1-dimethyl-N-phenylindole-2-carboxamide

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:264.126263138
Heavy Atom Count:20
Complexity:351

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of N,1-dimethyl-N-phenylindole-2-carboxamide

There total 8 articles about N,1-dimethyl-N-phenylindole-2-carboxamide 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: 61.0%

: 160153-65-1
N-methyl-N-phenyl-5-(3-methoxymethyl)indole-2-carboxamide

: 62048-33-3
N-methyl-N-phenyl-1-methyl-1H-indole-2-carboxamide

Guidance literature:: With aluminum tri-bromide; thiophenol; In dichloromethane; 0 deg C, 3 h, then room temp., 48 h;
DOI:10.1016/S0040-4020(01)89350-9

Reference yield: 58.0%

: 62048-32-2
N-methyl-N-phenyl-1H-indole-2-carboxamide

: 74-88-4
methyl iodide

: 62048-33-3
N-methyl-N-phenyl-1-methyl-1H-indole-2-carboxamide

Guidance literature:: With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; water; at 25 ℃; for 3h;
DOI:10.1016/j.bmc.2008.09.072

Reference yield: 31.0%

: 603-76-9
1-methylindole

: 190511-51-4
N-methyl-N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide

: 62048-33-3
N-methyl-N-phenyl-1-methyl-1H-indole-2-carboxamide

Guidance literature:: With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.25h;

1-methylindole; N-methyl-N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide; In tetrahydrofuran; at -78 ℃; for 16h;
DOI:10.1039/a809181a