• Product NameMequindox
  • CasNo. 13297-17-1
  • MFC11H10 N2 O3
  • MW218.212
  • Purity
  • Appearance
  • Packing
  • Contact usInquiry

Product Details

CasNo: 13297-17-1

MF: C11H10 N2 O3

Quality Manufacturer Supply High Purity 99% Mequindox 13297-17-1 with Reasonable Price

  • Molecular Formula:C11H10 N2 O3
  • Molecular Weight:218.212
  • Melting Point:153-154 °C 
  • Boiling Point:°Cat760mmHg 
  • PKA:1.63±0.30(Predicted) 
  • Flash Point:°C 
  • PSA:67.99000 
  • Density:g/cm3 
  • LogP:2.20780 

2-ACETYL-3-METHYLQUINOXALINEDIIUM-1,4-DIOLATE(Cas 13297-17-1) Usage

InChI:InChI=1/C11H10N2O3/c1-7-11(8(2)14)13(16)10-6-4-3-5-9(10)12(7)15/h3-6H,1-2H3

13297-17-1 Relevant articles

Effective promotion of beirut reaction by-cyclodextrin in water

Sun, Tao,Zhao, Wen-Jing,Hao, Ai-You,Sun, Li-Zhen

, p. 3097 - 3105 (2011)

A mild and highly efficient, environment...

Thermochemical and Theoretical Study of Some Quinoxaline 1,4-Dioxides and of Pyrazine 1,4-Dioxide

Acree Jr.,Powell, Joyce R.,Tucker, Sheryl A.,Ribeiro da Silva, Maria D.M.C.,Matos, M. Agostinha R.,Goncalves,Santos,Morais,Pilcher

, p. 3722 - 3726 (1997)

The following standard molar enthalpies ...

Synthesis, 3D-QSAR analysis and biological evaluation of quinoxaline 1,4-di-N-oxide derivatives as antituberculosis agents

Pan, Yuanhu,Li, Panpan,Xie, Shuyu,Tao, Yanfei,Chen, Dongmei,Dai, Menghong,Hao, Haihong,Huang, Lingli,Wang, Yulian,Wang, Liye,Liu, Zhenli,Yuan, Zonghui

, p. 4146 - 4153 (2016)

A series of quinoxaline 1,4-di-N-oxide d...

-

Issidorides,Haddadin

, p. 4067 (1966)

-

Preparation method of mequindox

-

Paragraph 0046-0063, (2019/02/08)

The invention provides a preparation met...

Improved synthesis of quinocetone and its two deoxy metabolites

Li, Yuwen,Qiu, Mei,Bai, Yubin,Qu, Shaoqi,Hao, Zhihui

, p. 265 - 270 (2018/04/12)

Oxidation of o-nitroaniline with sodium ...

Preparation method of quinohydroxylone

-

Paragraph 0021; 0045, (2016/10/10)

The invention relates to a preparation m...

13297-17-1 Process route

benzofurazan oxide
480-96-6,68100-26-5

benzofurazan oxide

acetylacetone
123-54-6,81235-32-7

acetylacetone

3-methyl-2-acetylquinoxaline-1,4-dioxide
13297-17-1

3-methyl-2-acetylquinoxaline-1,4-dioxide

Conditions
Conditions Yield
With triethylamine; In ethanol; at 45 ℃; for 2h;
94%
With triethylamine; In ethanol; for 3h; Ambient temperature;
86%
With silica gel; for 0.0666667h; Microwave irradiation;
85%
With triethylamine; In dichloromethane; at 25 ℃; for 12h;
80%
With triethylamine; at 60 ℃; for 4h; Temperature;
79.3%
With triethylamine; In ethanol; at 20 ℃; for 24h;
78%
With triethylamine; In chloroform; at 20 ℃; for 24h;
73%
benzofurazan oxide; With β‐cyclodextrin; In methanol; water; for 0.5h;
acetylacetone; In methanol; water; at 20 ℃; for 0.333333h;
61%
With Wako gel C-200; for 168h;
58%
With 3 A molecular sieve; In ethanol; at 90 ℃;
58%
With trimethylamine; for 24h; Ambient temperature;
 
In triethylamine;
 
With aminoethyl alcohol; calcium chloride;
 
at 20 - 35 ℃; for 20h;
 
2-methyl-3-acetylquinoxaline
22059-64-9

2-methyl-3-acetylquinoxaline

3-methyl-2-acetylquinoxaline-1,4-dioxide
13297-17-1

3-methyl-2-acetylquinoxaline-1,4-dioxide

2-Acetyl-3-methylquinoxaline 1-Oxide
61522-57-4

2-Acetyl-3-methylquinoxaline 1-Oxide

Conditions
Conditions Yield
With xylene; for 18h; Heating;
55.5%
2.3%
19.8%

13297-17-1 Upstream products

  • 480-96-6
    480-96-6

    benzofurazan oxide

  • 123-54-6
    123-54-6

    acetylacetone

  • 110-13-4
    110-13-4

    2,5-hexanedione

  • 1322877-87-1
    1322877-87-1

    C6H4N2O2*C42H70O35

13297-17-1 Downstream products

  • 61522-56-3
    61522-56-3

    3-Acetyl-2-methylquinoxaline 1-Oxide

  • 22059-64-9
    22059-64-9

    2-methyl-3-acetylquinoxaline

  • 61522-57-4
    61522-57-4

    2-Acetyl-3-methylquinoxaline 1-Oxide

  • 85108-69-6
    85108-69-6

    2-[3-(4-chlorophenyl)-2-propenoyl]-3-methylquinoxaline-1,4-dioxide

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