3,8-Diamino-6-(3-methoxyphenyl)-5-methylphenanthridinium bromide

Base Information

Chemical Name:3,8-Diamino-6-(3-methoxyphenyl)-5-methylphenanthridinium bromide
CAS No.:79053-79-5
Molecular Formula:Br*C₂₁H₂₀N₃O
Molecular Weight:410.313
Hs Code.:
ChEMBL ID:CHEMBL26589

Synonyms:3,8-Diamino-6-(3-methoxyphenyl)-5-methylphenanthridinium bromide;CHEMBL26589;Phenanthridinium, 3,8-diamino-6-(3-methoxyphenyl)-5-methyl-, bromide

Suppliers and Price of 3,8-Diamino-6-(3-methoxyphenyl)-5-methylphenanthridinium bromide

Supply Marketing:

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

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Chemical Property of 3,8-Diamino-6-(3-methoxyphenyl)-5-methylphenanthridinium bromide

Chemical Property:

Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:409.07897
Heavy Atom Count:26
Complexity:458

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[N+]1=C2C=C(C=CC2=C3C=CC(=CC3=C1C4=CC(=CC=C4)OC)N)N.[Br-]

Technology Process of 3,8-Diamino-6-(3-methoxyphenyl)-5-methylphenanthridinium bromide

There total 2 articles about 3,8-Diamino-6-(3-methoxyphenyl)-5-methylphenanthridinium bromide 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:

: 79053-78-4
N-(4,4'-Dinitro-biphenyl-2-yl)-3-methoxy-benzamide

: 79053-79-5
3,8-Diamino-6-(3-methoxy-phenyl)-5-methyl-phenanthridinium; bromide

Guidance literature:: Multi-step reaction with 2 steps

1: 66 percent / POCl₃ / nitrobenzene / Heating

2: 2.) aq. HBr, Fe

With hydrogen bromide; iron; trichlorophosphate; In nitrobenzene;
DOI:10.1021/jm00143a014