6-Chloro-3,4-diphenylquinoline

Base Information

Chemical Name:6-Chloro-3,4-diphenylquinoline
CAS No.:61554-25-4
Molecular Formula:C21H14ClN
Molecular Weight:315.802
Hs Code.:
DSSTox Substance ID:DTXSID20491830
Nikkaji Number:J3.450.703A
Wikidata:Q82336862

Synonyms:6-Chloro-3,4-diphenylquinoline;61554-25-4;SCHEMBL8956546;DTXSID20491830

Suppliers and Price of 6-Chloro-3,4-diphenylquinoline

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 6-Chloro-3,4-diphenylquinoline

Chemical Property:

XLogP3:6.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:315.0814771
Heavy Atom Count:23
Complexity:372

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CN=C3C=CC(=CC3=C2C4=CC=CC=C4)Cl

Technology Process of 6-Chloro-3,4-diphenylquinoline

There total 5 articles about 6-Chloro-3,4-diphenylquinoline 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: 83.0%

: 27032-10-6
4-chlorobenzyl azide

: 501-65-5
diphenyl acetylene

: 61554-25-4
6-chloro-3,4-diphenylquinoline

Guidance literature:: With copper(II) bis(trifluoromethanesulfonate); In nitromethane; at 80 ℃; for 24h; regioselective reaction; Sealed tube; Inert atmosphere;
DOI:10.1039/c5ra23065a

Reference yield: 69.0%

: 122-78-1
phenylacetaldehyde

: 719-64-2
5-chloro-3-phenylanthranil

: 61554-25-4
6-chloro-3,4-diphenylquinoline

Guidance literature:: With oxygen; silver trifluoromethanesulfonate; copper; at 110 ℃; for 30h; Schlenk technique;

Reference yield: 69.0%

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

: 719-59-5
5-chloro-2-aminobenzophenone

: 61554-25-4
6-chloro-3,4-diphenylquinoline

Guidance literature:: With palladium(II) trifluoroacetate; oxygen; copper(II) bis(trifluoromethanesulfonate); trifluoroacetic acid; In chlorobenzene; at 110 ℃; regioselective reaction;
DOI:10.1039/c5cc05196g