2-Cyano-3-(3-chlorophenylthiomethyl)pyridine

Base Information

Chemical Name:2-Cyano-3-(3-chlorophenylthiomethyl)pyridine
CAS No.:126570-66-9
Molecular Formula:C13H9ClN2S
Molecular Weight:260.747
Hs Code.:
DSSTox Substance ID:DTXSID201206954
Mol file:126570-66-9.mol

Synonyms:126570-66-9;2-CYANO-3-(3-CHLOROPHENYLTHIOMETHYL)PYRIDINE;SCHEMBL6992287;NUDWKSIYWTZGSN-UHFFFAOYSA-N;DTXSID201206954;AKOS012216355;3-[[(3-Chlorophenyl)thio]methyl]-2-pyridinecarbonitrile

Suppliers and Price of 2-Cyano-3-(3-chlorophenylthiomethyl)pyridine

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-Cyano-3-(3-chlorophenylthiomethyl)pyridine

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:260.0174972
Heavy Atom Count:17
Complexity:288

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Cl)SCC2=C(N=CC=C2)C#N

Technology Process of 2-Cyano-3-(3-chlorophenylthiomethyl)pyridine

There total 2 articles about 2-Cyano-3-(3-chlorophenylthiomethyl)pyridine 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:

: 2037-31-2
3-chlorophenylthiol

: 116986-13-1
2-cyano-3-(bromomethyl)pyridine

: 126570-66-9
3-[(3-chlorophenyl)thiomethyl]-2-cyanopyridine

Guidance literature:: With sodium methylate; In methanol;

Reference yield:

: 20970-75-6
2-cyano-3-methylpyridine

: 126570-66-9
3-[(3-chlorophenyl)thiomethyl]-2-cyanopyridine

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane

2: sodium methylate / methanol

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium methylate; In methanol; tetrachloromethane;