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2-Chloroquinoxaline
Base Information
- Chemical Name: 2-Chloroquinoxaline
- CAS No.: 1448-87-9
Reputable factory supply 2-Chloroquinoxaline 1448-87-9 in bulk at low price
- Molecular Formula: C8H5ClN2
- Molecular Weight: 164.594
- Vapor Pressure: 0.03mmHg at 25°C
- Melting Point: 47-50 °C(lit.)
- Refractive Index: 1.662
- Boiling Point: 252.919 °C at 760 mmHg
- PKA: -1.21±0.30(Predicted)
- Flash Point: 131.229 °C
- PSA： 25.78000
- Density: 1.35 g/cm3
- LogP: 2.28320
2-Chloroquinoxaline(Cas 1448-87-9) Usage
InChI:InChI=1/C8H5ClN2/c9-8-5-10-6-3-1-2-4-7(6)11-8/h1-5H
1448-87-9 Relevant articles
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Castle,R.N.,Onda,M.
, p. 954 - 956 (1961)
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Synthesis of new quinoxaline derivatives
Makhloufi,Baitiche,Merbah,Benachour
, p. 3532 - 3540 (2011)
New quinoxaline derivatives were prepare...
An improved method for chlorination of nitrogen-containing π-deficient heteroaromatics using triphenylphosphine and trichloroisocyanuric acid
Sugimoto, Osamu,Tanji, Ken-ichi
, p. 181 - 185 (2005)
Phosphorus compound prepared by reaction...
Synthesis and antimicrobial activity of some 2(1H)-quinoxalinone-6-sulfonyl derivatives
Obafemi, Craig A.,Akinpelu
, p. 1795 - 1807 (2005)
The synthesis of some quinoxalinesulfony...
Novel gas-phase cyclisation reactions of 2-(1-pyrazolyl)phenylnitrenes
Clark, Bernard A. J.,McNab, Hamish,Sommerville, Craig C.
, p. 1211 - 1212 (1996)
Flash vacuum pyrolysis of the azide 3 gi...
Synthesis, antiviral and antibacterial activities and action mechanism of penta-1,4-dien-3-one oxime ether derivatives containing a quinoxaline moiety
Xia, Rongjiao,Guo, Tao,Chen, Mei,Su, Shijun,He, Jun,Tang, Xu,Jiang, Shichun,Xue, Wei
, p. 16461 - 16467 (2019)
A series of penta-1,4-dien-3-one oxime e...
A Computer-Driven Scaffold-Hopping Approach Generating New PTP1B Inhibitors from the Pyrrolo[1,2-a]quinoxaline Core
García-Marín, Javier,Griera, Mercedes,Alajarín, Ramón,Rodríguez-Puyol, Manuel,Rodríguez-Puyol, Diego,Vaquero, Juan J.
, p. 2895 - 2906 (2021/07/21)
Protein tyrosine phosphatase 1B (PTP1B) ...
Design and Synthesis of Some New N-Phenyl-[1,2,4]triazolo[4,3-a]quinoxaline-1-sulfonamide Derivatives and Their Anti-Cancer Activity
Badithapuram, Vinitha,Bandari, Srinivas,Dasari, Gouthami,Nukala, Satheesh Kumar,Pandiri, Madhuri
, p. 2280 - 2285 (2021/12/23)
Abstract: Synthesis of some new derivati...
One-pot multicomponent synthesis of novel 2-(piperazin-1-yl) quinoxaline and benzimidazole derivatives, using a novel sulfamic acid functionalized Fe3O4 MNPs as highly effective nanocatalyst
Esam, Zohreh,Akhavan, Malihe,Bekhradnia, Ahmadreza
, (2020/10/27)
The immobilization of sulfonic acid on t...
Multifunctional quinoxaline-hydrazone derivatives with acetylcholinesterase and monoamine oxidases inhibitory activities as potential agents against Alzheimer’s disease
Ilgin, Sinem,Karaduman, Abdullah Burak,Levent, Serkan,Osmaniye, Derya,?avu?o?lu, Betül Kaya,?evik, Ulviye Acar,?zkay, Yusuf,Kaplancikli, Zafer As?m,Karaburun, Ahmet ?a?r?,Sa?lik, Begüm Nurpelin,Turan, Gülhan
, p. 1000 - 1011 (2020/04/29)
Multitarget molecules are considered as ...
1448-87-9 Process route
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120569-15-5
C22 H15 N3 O2
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1448-87-9
2-chloroquinoxaline
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119-61-9
benzophenone
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67-72-1
hexachloroethane
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983-79-9
benzophenone azine
| Conditions | Yield |
|---|---|
|
With
tetrachloromethane;
Yields of byproduct given;
Ambient temperature;
Irradiation;
|
74%
|
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51-17-2,79351-71-6
benzoimidazole
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67-66-3,8013-54-5
chloroform
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1448-87-9
2-chloroquinoxaline
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91-15-6
phthalonitrile
| Conditions | Yield |
|---|---|
|
at 390 - 400 ℃;
|
88%
12% |
1448-87-9 Upstream products
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1196-57-2
quinoxalin-2(1) -one
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6935-29-1
quinoxaline-N-oxide
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20254-76-6
3-Chloroquinoxaline-2-carboxylic acid
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51-17-2
benzoimidazole
1448-87-9 Downstream products
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57315-47-6
2-ethoxyquinoxaline
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102956-19-4
N -(4-quinoxalin-2-ylamino-benzoyl)-L-glutamic acid diethyl ester
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52598-53-5
Phenoxy-2 quinoxaline
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100962-02-5
4-quinoxalin-2-ylamino-benzoic acid