2H-Isoindole-2-hexanamide, 1,3-dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)-

Base Information

Chemical Name:2H-Isoindole-2-hexanamide, 1,3-dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)-
CAS No.:138349-41-4
Molecular Formula:C₂₉H₂₇N₃O₃
Molecular Weight:465.552
Hs Code.:
DSSTox Substance ID:DTXSID10160624
Nikkaji Number:J440.280D
Wikidata:Q83028983

Synonyms:BRN 5462349;2H-Isoindole-2-hexanamide, 1,3-dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)-;1,3-Dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)-2H-isoindole-2-hexanamide;138349-41-4;2H-Isoindole-2-hexanamide, 1,3-dihydro-N-(3-methyl-1-phenyl-1H-indol-2-yl)-1,3-dioxo-;DTXSID10160624;C29H27N3O3;C29-H27-N3-O3;LS-84679;N-(1-Phenyl-3-methyl-1H-indol-2-yl)-6-(1,3-dioxoisoindolin-2-yl)hexanamide

Suppliers and Price of 2H-Isoindole-2-hexanamide, 1,3-dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)-

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
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Total 1 raw suppliers

Chemical Property of 2H-Isoindole-2-hexanamide, 1,3-dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)-

Chemical Property:

Vapor Pressure:3.65E-15mmHg at 25°C
Boiling Point:617.2°Cat760mmHg
Flash Point:327.1°C
Density:1.24g/cm³
XLogP3:5.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:465.20524173
Heavy Atom Count:35
Complexity:755

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N(C2=CC=CC=C12)C3=CC=CC=C3)NC(=O)CCCCCN4C(=O)C5=CC=CC=C5C4=O

Technology Process of 2H-Isoindole-2-hexanamide, 1,3-dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)-

There total 2 articles about 2H-Isoindole-2-hexanamide, 1,3-dihydro-1,3-dioxo-N-(3-methyl-1-phenyl-1H-indol-2-yl)- 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:

: 31968-60-2
6-phthalimidohexanoyl chloride

: 138349-58-3
3-Methyl-1-phenyl-1H-indol-2-ylamine; hydrochloride

: 138349-41-4
6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic acid (3-methyl-1-phenyl-1H-indol-2-yl)-amide

Guidance literature:: With triethylamine; In dichloromethane; at 5 ℃; Yield given;
DOI:10.1007/BF00767254

Reference yield:

: 4443-26-9
6-phthalimidohexanoic acid

: 138349-41-4
6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic acid (3-methyl-1-phenyl-1H-indol-2-yl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂, DMF / CH₂Cl₂ / 2 h / Heating

2: Et₃N / CH₂Cl₂ / 5 °C

With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In dichloromethane;
DOI:10.1007/BF00767254