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  • Product Name2,6-DIMETHYLQUINOLINE
  • CasNo. 877-43-0
  • MFC11H11N
  • MW157.215
  • Purity
  • Appearancewhite to light yellow crystal powder
  • Packing
  • Contact usInquiry

Product Details

CasNo： 877-43-0

MF： C11H11N

Appearance： white to light yellow crystal powder

Factory Supply Industrial Grade 2,6-DIMETHYLQUINOLINE 877-43-0 with Best Price

  • Molecular Formula:C11H11N
  • Molecular Weight:157.215
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.0142mmHg at 25°C 
  • Melting Point:57-59 °C(lit.) 
  • Refractive Index:1.61 
  • Boiling Point:266.5 °C at 760 mmHg 
  • PKA:pK1:5.46(+1) (25°C) 
  • Flash Point:106.5 °C 
  • PSA：12.89000 
  • Density:1.052 g/cm3 
  • LogP:2.85160 

2,6-DIMETHYLQUINOLINE(Cas 877-43-0) Usage

Biochem/physiol Actions

2,6-Dimethylquinoline is the chemical constituent present in roots of Peucedantu praeruptorum. It is a potential inhibitor of cytochrome P450 1A2 activity.

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

877-43-0 Relevant articles

1H, 13C and 15N NMR and GIAO CPHF calculations on two quinoacridinium salts

Jaroszewska-Manaj, Jolanta,Maciejewska, Dorota,Wawer, Iwona

, p. 482 - 485 (2000)

The complete 1H, 13C and 15N NMR assignm...

Oxidation of 1,2-dihydroquinolines under mild and heterogeneous conditions

Damavandi,Zolfigol,Karami

, p. 3183 - 3187 (2001)

A combination of NaHSO4.H2O and Na2Cr2O7...

Highly Chemoselective Deoxygenation of N-Heterocyclic N-Oxides Using Hantzsch Esters as Mild Reducing Agents

An, Ju Hyeon,Kim, Kyu Dong,Lee, Jun Hee

supporting information, p. 2876 - 2894 (2021/02/01)

Herein, we disclose a highly chemoselect...

Metal-Free Deoxygenation of Amine N-Oxides: Synthetic and Mechanistic Studies

Lecroq, William,Schleinitz, Jules,Billoue, Mallaury,Perfetto, Anna,Gaumont, Annie-Claude,Lalevée, Jacques,Ciofini, Ilaria,Grimaud, Laurence,Lakhdar, Sami

, p. 1237 - 1242 (2021/06/01)

We report herein an unprecedented combin...

Method for producing quinoline derivative through one-pot two-step method

-

Paragraph 0033-0036, (2020/02/17)

The invention relates to a method for pr...

Method for preparing quinoline compound through oxidation and reduction integration (by machine translation)

-

Paragraph 9-10, (2020/02/17)

The method takes the aromatic nitro comp...

877-43-0 Process route

<i>p</i>-toluidine
106-49-0,12221-03-3

p-toluidine

ethyl vinyl ether
109-92-2,25104-37-4

ethyl vinyl ether

2,6-dimethylquinoline
877-43-0

2,6-dimethylquinoline

N-ethyl-p-tolylamine
622-57-1

N-ethyl-p-tolylamine

Conditions
Conditions Yield
With palladium on activated charcoal; palladium dichloride; In acetonitrile; at 80 ℃; for 24h;
82 %Chromat.
12 %Chromat.
1.3-butanediol
18826-95-4,107-88-0

1.3-butanediol

<i>p</i>-toluidine
106-49-0,12221-03-3

p-toluidine

4,6-dimethylquinoline
826-77-7

4,6-dimethylquinoline

2,6-dimethylquinoline
877-43-0

2,6-dimethylquinoline

Conditions
Conditions Yield
With iron(III) chloride hexahydrate; In tetrachloromethane; at 150 ℃; for 8h; Overall yield = 93 %; Inert atmosphere;

877-43-0 Upstream products

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    3-oxobutyraldehyde

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    106-49-0

    p-toluidine

877-43-0 Downstream products

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    2-(6-methyl-1H-[2]chinolyLiDene)-indane-1,3-dione

  • 67866-68-6
    67866-68-6

    6-methyl-2-(3-nitro-styryl)-quinoline

  • 67866-69-7
    67866-69-7

    (E)-6-methyl-2-(4-nitrostyryl)quinoline

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