2(1H)-Pyrazinone, 3,5-dichloro-6-phenyl-1-(phenylmethyl)-

Base Information

Chemical Name:2(1H)-Pyrazinone, 3,5-dichloro-6-phenyl-1-(phenylmethyl)-
CAS No.:138610-71-6
Molecular Formula:C17H12Cl2N2O
Molecular Weight:331.201
Hs Code.:
DSSTox Substance ID:DTXSID00357288
Nikkaji Number:J1.215.784C
Wikidata:Q82137149

Synonyms:138610-71-6;2(1H)-Pyrazinone, 3,5-dichloro-6-phenyl-1-(phenylmethyl)-;DTXSID00357288

Suppliers and Price of 2(1H)-Pyrazinone, 3,5-dichloro-6-phenyl-1-(phenylmethyl)-

Supply Marketing:

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

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Chemical Property of 2(1H)-Pyrazinone, 3,5-dichloro-6-phenyl-1-(phenylmethyl)-

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:330.0326684
Heavy Atom Count:22
Complexity:489

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN2C(=C(N=C(C2=O)Cl)Cl)C3=CC=CC=C3

Technology Process of 2(1H)-Pyrazinone, 3,5-dichloro-6-phenyl-1-(phenylmethyl)-

There total 3 articles about 2(1H)-Pyrazinone, 3,5-dichloro-6-phenyl-1-(phenylmethyl)- 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:

: 100-52-7
benzaldehyde

: 138610-71-6
1-benzyl-3,5-dichloro-6-phenyl-2(1H)-pyrazinone

Guidance literature:: Multi-step reaction with 2 steps

1: triethylammonium chloride / chlorobenzene

With triethylamine hydrochloride; In chlorobenzene; 1: Strecker synthesis;
DOI:10.1016/j.tet.2004.09.054

Reference yield:

: 100-46-9
benzylamine

: 138610-71-6
1-benzyl-3,5-dichloro-6-phenyl-2(1H)-pyrazinone

Guidance literature:: Multi-step reaction with 2 steps

1: triethylammonium chloride / chlorobenzene

With triethylamine hydrochloride; In chlorobenzene; 1: Strecker synthesis;
DOI:10.1016/j.tet.2004.09.054