4-Chloro-3-phenylquinoline

Base Information

Chemical Name:4-Chloro-3-phenylquinoline
CAS No.:6319-32-0
Molecular Formula:C15H10 Cl N
Molecular Weight:239.704
Hs Code.:
NSC Number:31021
DSSTox Substance ID:DTXSID30283349
Wikidata:Q82017886

Synonyms:4-chloro-3-phenylquinoline;6319-32-0;NSC31021;SCHEMBL15646666;DTXSID30283349;NSC-31021;AKOS025149603

Suppliers and Price of 4-Chloro-3-phenylquinoline

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 7 raw suppliers

Chemical Property of 4-Chloro-3-phenylquinoline

Chemical Property:

Vapor Pressure:6.46E-05mmHg at 25°C
Boiling Point:355.3°Cat760mmHg
Flash Point:199.8°C
Density:1.235g/cm³
XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:239.0501770
Heavy Atom Count:17
Complexity:249

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=C(C3=CC=CC=C3N=C2)Cl

Technology Process of 4-Chloro-3-phenylquinoline

There total 7 articles about 4-Chloro-3-phenylquinoline 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: 88.0%

: 25410-99-5
3-phenylquinolin-4(1H)-one

: 6319-32-0
4-chloro-3-phenylquinoline

Guidance literature:: With trichlorophosphate; for 2h; Reflux;

Reference yield: 50.0%

: 611-35-8
4-chloroquinoline

: 108-86-1,52753-63-6
bromobenzene

: 6319-32-0
4-chloro-3-phenylquinoline

Guidance literature:: With 2,2-dimethylhexanoic acid; butyl di-1-adamantylphosphine tetrafluoroborate; palladium diacetate; caesium carbonate; silver carbonate; In toluene; at 120 ℃; for 22h; regioselective reaction; Inert atmosphere;
DOI:10.1021/ja206022p