1,4-Bis(heptyloxy)-6-methyl-6H-indolo[2,3-b]quinoxaline

Base Information

Chemical Name:1,4-Bis(heptyloxy)-6-methyl-6H-indolo[2,3-b]quinoxaline
CAS No.:77855-17-5
Molecular Formula:C₂₉H₃₉N₃O₂
Molecular Weight:461.648
Hs Code.:
DSSTox Substance ID:DTXSID50507251
Wikidata:Q82363369

Synonyms:77855-17-5;1,4-Bis(heptyloxy)-6-methyl-6H-indolo[2,3-b]quinoxaline;DTXSID50507251;1,4-diheptyloxy-6-methylindolo[2,3-b]quinoxaline

Suppliers and Price of 1,4-Bis(heptyloxy)-6-methyl-6H-indolo[2,3-b]quinoxaline

Supply Marketing:

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

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Chemical Property of 1,4-Bis(heptyloxy)-6-methyl-6H-indolo[2,3-b]quinoxaline

Chemical Property:

XLogP3:8.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:14
Exact Mass:461.30422750
Heavy Atom Count:34
Complexity:576

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCOC1=C2C(=C(C=C1)OCCCCCCC)N=C3C(=N2)C4=CC=CC=C4N3C

Technology Process of 1,4-Bis(heptyloxy)-6-methyl-6H-indolo[2,3-b]quinoxaline

There total 2 articles about 1,4-Bis(heptyloxy)-6-methyl-6H-indolo[2,3-b]quinoxaline 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:

: 77855-11-9
1,4-Diheptyloxy-2,3-dinitrobenzene

: 77855-17-5
1,4-diheptyloxy-6-methylindolo<2,3-b>quinoxaline

: 77855-23-3
4,7-diheptyloxy-1-methylspiro(2H-benzimidazole-2,3'-indolin)-2'-one

: 77855-25-5
Bis-(3,6-bis-heptyloxy-2-nitro-phenyl)-diazene

Guidance literature:: With hydrogenchloride; iron; Yield given. Multistep reaction. Yields of byproduct given; 1) EtOH, 2) 50percent acetic acid;
DOI:10.1007/BF00507254

Reference yield:

: 2058-74-4
1-methyl-1H-indole-2,3-dione

: 77855-11-9
1,4-Diheptyloxy-2,3-dinitrobenzene

: 77855-17-5
1,4-diheptyloxy-6-methylindolo<2,3-b>quinoxaline

: 77855-23-3
4,7-diheptyloxy-1-methylspiro(2H-benzimidazole-2,3'-indolin)-2'-one

: 77855-25-5
Bis-(3,6-bis-heptyloxy-2-nitro-phenyl)-diazene

Guidance literature:: With hydrogenchloride; iron; Yield given. Multistep reaction. Yields of byproduct given; 1) EtOH, 2) 50percent acetic acid;
DOI:10.1007/BF00507254