2-[2-(4-Chlorophenyl)ethynyl]pyridine

Base Information

Chemical Name:2-[2-(4-Chlorophenyl)ethynyl]pyridine
CAS No.:80221-12-1
Molecular Formula:C₁₃H₈ClN
Molecular Weight:213.666
Hs Code.:
DSSTox Substance ID:DTXSID901285250
Nikkaji Number:J2.376.317F

Synonyms:DTXSID901285250;2-[2-(4-chlorophenyl)ethynyl]pyridine;80221-12-1

Suppliers and Price of 2-[2-(4-Chlorophenyl)ethynyl]pyridine

Supply Marketing:

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

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Chemical Property of 2-[2-(4-Chlorophenyl)ethynyl]pyridine

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:213.0345270
Heavy Atom Count:15
Complexity:254

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

Canonical SMILES:C1=CC=NC(=C1)C#CC2=CC=C(C=C2)Cl

Technology Process of 2-[2-(4-Chlorophenyl)ethynyl]pyridine

There total 2 articles about 2-[2-(4-Chlorophenyl)ethynyl]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:

: 80221-12-1
2-(4-chloro-phenylethynyl)-pyridine

Guidance literature:: With potassium hydroxide;
DOI:10.1021/ja01192a009

Reference yield:

: C₁₃H₁₀Br₂ClN

: 80221-12-1
2-(4-chloro-phenylethynyl)-pyridine

Guidance literature:: With potassium hydroxide; In ethanol; Reflux;
DOI:10.1016/j.jphotochem.2013.07.004

Reference yield: 93.0%

: 80221-12-1
2-(4-chloro-phenylethynyl)-pyridine

: 24470-01-7,5343-70-4
(E)-2-(4-chlorostyryl)pyridine

Guidance literature:: With water; potassium ethyl xanthogenate; In N,N-dimethyl-formamide; at 130 ℃; for 12h; stereoselective reaction; Schlenk technique;
DOI:10.1039/C9CC00128J