3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one

Base Information

Chemical Name:3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one
CAS No.:129972-91-4
Molecular Formula:C₁₅H₉ClO
Molecular Weight:240.689
Hs Code.:
DSSTox Substance ID:DTXSID201265326
Nikkaji Number:J329.192H

Synonyms:SCHEMBL9189694;DTXSID201265326;129972-91-4;3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one

Suppliers and Price of 3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one

Supply Marketing:

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

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Chemical Property of 3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:240.0341926
Heavy Atom Count:17
Complexity:329

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C#CC2=CC=CC=C2Cl

Technology Process of 3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one

There total 15 articles about 3-(2-Chlorophenyl)-1-phenyl-2-propyn-1-one 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: 95.0%

: 873-31-4
2-chlorophenylacetylene

: 98-88-4
benzoyl chloride

: 129972-91-4
3-(2-chlorophenyl)-1-phenylprop-2-yn-1-one

Guidance literature:: With copper(l) iodide; N,N,N,N,-tetramethylethylenediamine; triethylamine; at 20 ℃; for 1h; Schlenk technique; Inert atmosphere;
DOI:10.1055/s-0034-1378358

Reference yield: 89.0%

: 16619-64-0
1-(2-chlorophenyl)-3-phenyl-2-propyn-1-one

: 129972-91-4
3-(2-chlorophenyl)-1-phenylprop-2-yn-1-one

Guidance literature:: With silver tetrafluoroborate; tris(2,4-di-tert-butylphenyl)phosphite gold(I) chloride; In 1,2-dichloro-ethane; at 20 ℃; for 2h; regioselective reaction; Inert atmosphere; Schlenk technique; Glovebox;
DOI:10.1021/ja504892c

Reference yield: 87.0%

: 6125-26-4
phenyl(2-phenyl-2,3-dihydrobenzo[d]thiazol-2-yl)methanone

: 1-((2-chlorophenyl)ethynyl)-1λ³-benzo[d][1,2]iodaoxol-3(1H)-one

: 129972-91-4
3-(2-chlorophenyl)-1-phenylprop-2-yn-1-one

Guidance literature:: With sodium dihydrogenphosphate; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere; Irradiation;
DOI:10.1021/acs.orglett.9b01717