1H-Pyrrole-3-carbonitrile, 4-amino-2,5-diphenyl-

Base Information

Chemical Name:1H-Pyrrole-3-carbonitrile, 4-amino-2,5-diphenyl-
CAS No.:86625-51-6
Molecular Formula:C17H13N3
Molecular Weight:259.31
Hs Code.:
DSSTox Substance ID:DTXSID20434242
Nikkaji Number:J277.216G
Wikidata:Q82248593

Synonyms:86625-51-6;1H-Pyrrole-3-carbonitrile, 4-amino-2,5-diphenyl-;DTXSID20434242;2,5-Diphenyl-3-amino-1H-pyrrole-4-carbonitrile

Suppliers and Price of 1H-Pyrrole-3-carbonitrile, 4-amino-2,5-diphenyl-

Supply Marketing:

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

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Chemical Property of 1H-Pyrrole-3-carbonitrile, 4-amino-2,5-diphenyl-

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:259.110947427
Heavy Atom Count:20
Complexity:360

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=C(C(=C(N2)C3=CC=CC=C3)N)C#N

Technology Process of 1H-Pyrrole-3-carbonitrile, 4-amino-2,5-diphenyl-

There total 2 articles about 1H-Pyrrole-3-carbonitrile, 4-amino-2,5-diphenyl- 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: 76.0%

: 86625-48-1
4-cyano-2,5-diphenyl-3-nitropyrrole

: 86625-51-6
4-Amino-2,5-diphenyl-1H-pyrrole-3-carbonitrile

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; under 2327.2 Torr;

Reference yield:

: 67421-66-3
2,5-diphenyl-1H-pyrrole-3-carbonitrile

: 86625-51-6
4-Amino-2,5-diphenyl-1H-pyrrole-3-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / nitric acid, acetic anhydride / nitromethane / -15 °C

2: 76 percent / H₂ / 10percent Pd/C / ethanol / 2327.2 Torr

With hydrogen; nitric acid; acetic anhydride; palladium on activated charcoal; In nitromethane; ethanol;