• Product Name2,8-Dimethylquinoline
  • CasNo. 1463-17-8
  • MFC11H11N
  • MW157.215
  • Purity
  • Appearanceliquid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 1463-17-8

MF: C11H11N

Appearance: liquid

Factory Supply Industrial Grade 2,8-Dimethylquinoline 1463-17-8 with Best Price

  • Molecular Formula:C11H11N
  • Molecular Weight:157.215
  • Appearance/Colour:liquid 
  • Vapor Pressure:0.0263mmHg at 25°C 
  • Melting Point:61°C 
  • Refractive Index:1.61 
  • Boiling Point:255.299 °C at 760 mmHg 
  • PKA:5.87±0.50(Predicted) 
  • Flash Point:105.022 °C 
  • PSA:12.89000 
  • Density:1.053 g/cm3 
  • LogP:2.85160 

2,8-Dimethylquinoline(Cas 1463-17-8) Usage

InChI:InChI=1/C11H11N/c1-8-4-3-5-10-7-6-9(2)12-11(8)10/h3-7H,1-2H3

1463-17-8 Relevant articles

Photocatalytic tandem reaction of primary alcohols with arylamines in the synthesis of amides and alkylquinolines in the presence of a heterogeneous Fe(CrO2)2–TiO2/X system under aerobic conditions

Makhmutov

, p. 68 - 73 (2019)

A heterogeneous system Fe(CrO2)2–TiO2/X ...

Metal-Free Oxidative B?N Coupling of nido-Carborane with N-Heterocycles

Yang, Zhongming,Zhao, Weijia,Liu, Wei,Wei, Xing,Chen, Meng,Zhang, Xiao,Zhang, Xiaolei,Liang, Yong,Lu, Changsheng,Yan, Hong

supporting information, p. 11886 - 11892 (2019/07/18)

A general method for the oxidative subst...

Fe(CrO2)2-catalyzed, photoactivated oxidative one-pot tandem synthesis of substituted quinolines from primary alcohols and arylamines

Makhmutov, Aynur R.,Mustafin, Akhat G.,Usmanov, Salavat M.

, p. 369 - 374 (2018/05/28)

[Figure not available: see fulltext.] A ...

One-Pot Oxidative Synthesis of Substituted Quinolines from Alcohols and Arylamines Catalyzed by Fe(CrO2)2 in Water Medium

Makhmutov

, p. 1166 - 1172 (2018/10/24)

One-pot tandem synthesis was developed f...

1463-17-8 Process route

ethanol
64-17-5

ethanol

<i>o</i>-toluidine
95-53-4

o-toluidine

2,8-dimethylquinoline
1463-17-8

2,8-dimethylquinoline

Conditions
Conditions Yield
ethanol; With iron chromite; for 24h;
With dihydrogen peroxide; In water; at 20 ℃; for 2h; Irradiation;
o-toluidine; In water; at 20 ℃; for 0.0833333h;
94%
ethanol; With iron chromite; dihydrogen peroxide; In water; at 20 ℃; for 2h; UV-irradiation;
o-toluidine; In water; for 0.0833333h;
94%
With iron(III) chloride hexahydrate; In tetrachloromethane; at 140 ℃; for 4h; Autoclave; Inert atmosphere; Sealed tube;
85%
With copper(II) oxide; In water; at 25 ℃; UV-irradiation;
85%
With platinum-loaded TiO2 nanoparticles; at 30 ℃; for 4h; Irradiation; Inert atmosphere;
72%
With 2,4,6-trimethyl-pyridine; oxygen; palladium diacetate; trifluoroacetic acid; at 150 ℃; for 16h; Schlenk technique;
72%
With transition metal catalyst; pyridine derviative; acid derviative; at 150 ℃; for 16h; Green chemistry;
72%
With gold on titanium oxide; at 30 ℃; for 4h; UV-irradiation; Inert atmosphere;
68%
at 30 ℃; for 4h; UV-irradiation; Inert atmosphere;
acetaldehyde
75-07-0,9002-91-9

acetaldehyde

<i>o</i>-toluidine
95-53-4

o-toluidine

2,8-dimethylquinoline
1463-17-8

2,8-dimethylquinoline

Conditions
Conditions Yield
bis(1,5-cyclooctadiene)diiridium(I) dichloride; In dimethyl sulfoxide; at 90 ℃; for 17h;
74%
With di-μ-chlorobis(norbornadiene)dirhodium(I); nitrobenzene; In ethanol; at 180 ℃; for 4h;
24%
With hydrogenchloride; zinc(II) chloride;

1463-17-8 Upstream products

  • 636-21-5
    636-21-5

    o-toluidine hydrochloride

  • 75-07-0
    75-07-0

    acetaldehyde

  • 95-53-4
    95-53-4

    o-toluidine

  • 111-34-2
    111-34-2

    -butyl vinyl ether

1463-17-8 Downstream products

  • 67081-69-0
    67081-69-0

    2-acetylamino-3-methylbenzoic acid

  • 1446451-49-5
    1446451-49-5

    2,2'-(2-phenylpropane-1,3-diyl)bis(8-methylquinoline)

Relevant Products