Home > Products > Pharmaceutical intermediate

  • Product Name6-Methoxyquinoline
  • CasNo. 5263-87-6
  • MFC10H9NO
  • MW159.188
  • Purity
  • Appearancecolorless to light yellow liquid
  • Packing
  • Contact usInquiry

Product Details

CasNo： 5263-87-6

MF： C10H9NO

Appearance： colorless to light yellow liquid

Manufacturer Supply Best Quality 6-Methoxyquinoline 5263-87-6 with Efficient Transportation

  • Molecular Formula:C10H9NO
  • Molecular Weight:159.188
  • Appearance/Colour:colorless to light yellow liquid 
  • Vapor Pressure:0.00272mmHg at 25°C 
  • Melting Point:18-20 °C(lit.) 
  • Refractive Index:n20/D 1.625(lit.)  
  • Boiling Point:295.3 °C at 760 mmHg 
  • PKA:5.03(at 20℃) 
  • Flash Point:102.7 °C 
  • PSA：22.12000 
  • Density:1.13 g/cm3 
  • LogP:2.24340 

6-Methoxyquinoline(Cas 5263-87-6) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1584, 1946 DOI: 10.1021/ja01212a062

Definition

ChEBI: An aromatic ether that is quinoline substituted at position 6 by a methoxy group.

InChI:InChI=1/C10H9NO/c1-12-9-4-5-10-8(7-9)3-2-6-11-10/h2-7H,1H3

5263-87-6 Relevant articles

A NOVEL ROUTE TO QUINOLINE DERIVATIVES FROM 1,3-PROPANEDIOL AND AMINOARENES: RUTHENIUM CATALYZED HETEROCYCLIZATION UNDER NON-ACIDIC CONDITIONS

Tsuji, Yashushi,Nishimura, Hideo,Huh, Keun-Tae,Watanabe, Yoshihisa

, p. C44 - C46 (1985)

Ruthenium trichloride hydrate combined w...

-

Kaslow,Raymond

, p. 1102 (1946)

-

Organocatalytic Enantioselective Functionalization of Hydroxyquinolines through an Aza-Friedel-Crafts Alkylation with Isatin-derived Ketimines

Vila, Carlos,Rendón-Pati?o, Alejandra,Montesinos-Magraner, Marc,Blay, Gonzalo,Mu?oz, M. Carmen,Pedro, José R.

, p. 859 - 864 (2018)

A highly enantioselective addition of hy...

-

Auterhoff et al.

, p. 882,885,887 (1977)

-

Picomole-Scale Real-Time Photoreaction Screening: Discovery of the Visible-Light-Promoted Dehydrogenation of Tetrahydroquinolines under Ambient Conditions

Chen, Suming,Wan, Qiongqiong,Badu-Tawiah, Abraham K.

, p. 9345 - 9349 (2016)

The identification of new photocatalytic...

Method for realizing oxidative dehydrogenation of nitrogen-containing heterocyclic ring by using biomass-based carbon material

-

Paragraph 0010-0011; 0022-0023, (2021/06/26)

The invention provides a method for real...

Clean protocol for deoxygenation of epoxides to alkenes: Via catalytic hydrogenation using gold

Fiorio, Jhonatan L.,Rossi, Liane M.

, p. 312 - 318 (2021/01/29)

The epoxidation of olefin as a strategy ...

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...

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...

5263-87-6 Process route

6-methoxy-1,2,3,4-tetrahydroquinoline
120-15-0

6-methoxy-1,2,3,4-tetrahydroquinoline

2-nitro(ethylbenzene)
612-22-6

2-nitro(ethylbenzene)

6-methoxy quinoline
5263-87-6

6-methoxy quinoline

ortho-ethylaniline
578-54-1

ortho-ethylaniline

Conditions
Conditions Yield
With nickel-nitrogen-doped carbon framework; In water; at 145 ℃; for 18h; Inert atmosphere; Sealed tube; Green chemistry;
52%
48%
4-methoxyacetanilide
51-66-1

4-methoxyacetanilide

glycerol
56-81-5,25618-55-7,64333-26-2,8013-25-0

glycerol

6-hydroxyquinoline
580-16-5

6-hydroxyquinoline

6-methoxy quinoline
5263-87-6

6-methoxy quinoline

Conditions
Conditions Yield
With para-methoxynitrobenzene; sulfuric acid; boric acid; at 135 ℃;

5263-87-6 Upstream products

  • 580-16-5
    580-16-5

    6-hydroxyquinoline

  • 74-88-4
    74-88-4

    methyl iodide

  • 51-66-1
    51-66-1

    4-methoxyacetanilide

  • 56-81-5
    56-81-5

    glycerol

5263-87-6 Downstream products

  • 6334-31-2
    6334-31-2

    1-benzoyl-6-methoxy-1,2-dihydro-quinoline-2-carbonitrile

  • 34373-76-7
    34373-76-7

    1-ethyl-6-methoxyquinolin-1-ium iodide

  • 4789-73-5
    4789-73-5

    2-phenyl-6-methoxyquinoline

  • 101441-73-0
    101441-73-0

    3-benzyl-6-methoxy-quinoline

Relevant Products

Related products

  • Product NameCasNo.