Quinoline, 3-ethyl-2-phenyl-

Base Information

Chemical Name:Quinoline, 3-ethyl-2-phenyl-
CAS No.:101441-53-6
Molecular Formula:C17H15N
Molecular Weight:233.313
Hs Code.:
DSSTox Substance ID:DTXSID40396035
Nikkaji Number:J1.081.343C
Wikidata:Q82196495
Mol file:101441-53-6.mol

Synonyms:Quinoline, 3-ethyl-2-phenyl-;101441-53-6;2-Phenyl-3-ethylquinoline;SCHEMBL20081370;DTXSID40396035

Suppliers and Price of Quinoline, 3-ethyl-2-phenyl-

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
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price

Total 0 raw suppliers

Chemical Property of Quinoline, 3-ethyl-2-phenyl-

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:233.120449483
Heavy Atom Count:18
Complexity:256

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=CC2=CC=CC=C2N=C1C3=CC=CC=C3

Technology Process of Quinoline, 3-ethyl-2-phenyl-

There total 21 articles about Quinoline, 3-ethyl-2-phenyl- 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: 93.0%

: 100-52-7
benzaldehyde

: 123-72-8
butyraldehyde

: 62-53-3
aniline

: 101441-53-6
3-ethyl-2-phenylquinoline

Guidance literature:: With choline chloride; tin(ll) chloride; at 60 ℃; for 2h; Green chemistry;
DOI:10.1016/j.molliq.2016.04.094

Reference yield: 92.0%

: 5344-90-1
2-Aminobenzyl alcohol

: 495-40-9
propiophenone

: 101441-53-6
3-ethyl-2-phenylquinoline

Guidance literature:: With benzophenone; potassium tert-butylate; In 1,4-dioxane; at 90 ℃; for 0.5h; Inert atmosphere;
DOI:10.1021/jo801678n

Reference yield: 89.0%

: 5344-90-1
2-Aminobenzyl alcohol

: 495-41-0
1-phenylbut-2-en-1-one

: 101441-53-6
3-ethyl-2-phenylquinoline

: C₁₇H₁₉N

Guidance literature:: With C₁₉H₂₇ClIrN₃O⁽¹⁺⁾*Cl^(1-); potassium hydroxide; In water; at 100 ℃; for 18h; chemoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1055/a-1545-7563