2-(Methylsulfanyl)-4-(4-nitrophenyl)-6-phenylpyridine-3,5-dicarbonitrile

Base Information

Chemical Name:2-(Methylsulfanyl)-4-(4-nitrophenyl)-6-phenylpyridine-3,5-dicarbonitrile
CAS No.:86634-62-0
Molecular Formula:C20H12N4O2S
Molecular Weight:372.407
Hs Code.:
DSSTox Substance ID:DTXSID80513966
Wikidata:Q82374019

Synonyms:86634-62-0;DTXSID80513966;2-(Methylsulfanyl)-4-(4-nitrophenyl)-6-phenylpyridine-3,5-dicarbonitrile

Suppliers and Price of 2-(Methylsulfanyl)-4-(4-nitrophenyl)-6-phenylpyridine-3,5-dicarbonitrile

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-(Methylsulfanyl)-4-(4-nitrophenyl)-6-phenylpyridine-3,5-dicarbonitrile

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:372.06809681
Heavy Atom Count:27
Complexity:619

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CSC1=C(C(=C(C(=N1)C2=CC=CC=C2)C#N)C3=CC=C(C=C3)[N+](=O)[O-])C#N

Technology Process of 2-(Methylsulfanyl)-4-(4-nitrophenyl)-6-phenylpyridine-3,5-dicarbonitrile

There total 3 articles about 2-(Methylsulfanyl)-4-(4-nitrophenyl)-6-phenylpyridine-3,5-dicarbonitrile 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: 30.0%

: 86625-33-4
1,2-Dihydro-4-(4-nitrophenyl)-6-phenyl-2-thioxo-3,5-pyridinedicarbonitrile

: 74-88-4
methyl iodide

: 86634-62-0
2-Methylthio-4-(4-nitrophenyl)-6-phenyl-3,5-pyridinedicarbonitrile

Guidance literature:

Reference yield:

: 7357-70-2
Cyanothioacetamide

: 61222-95-5,101220-38-6,101220-27-3
2-Benzoyl-3-(4-nitrophenyl)-2-propenenitrile

: 74-88-4
methyl iodide

: 86634-62-0
2-Methylthio-4-(4-nitrophenyl)-6-phenyl-3,5-pyridinedicarbonitrile

Guidance literature:: With piperidine; Yield given. Multistep reaction; 1) methanol, room temp., 48h, 2) sodium methoxide, 2h;

Reference yield:

: 61222-95-5,101220-38-6,101220-27-3
2-Benzoyl-3-(4-nitrophenyl)-2-propenenitrile

: 86634-62-0
2-Methylthio-4-(4-nitrophenyl)-6-phenyl-3,5-pyridinedicarbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 27 percent / 2-hydroxyethanethiol / piperidine / methanol / Ambient temperature

2: 30 percent

With 2-hydroxyethanethiol; piperidine; In methanol;