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Structure

6-CHLOROQUINOXALINE

CAS
5448-43-1
Catalog Number
ACM5448431
Category
Other Products
Molecular Weight
164.59
Molecular Formula
C8H5ClN2

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Specification

Synonyms
6-Chloroquinoxaline, Quinoxaline, 6-chloro-, NSC17797, ZINC00046555, GL-1052, 5448-43-1, InChI=1/C8H5ClN2/c9-6-1-2-7-8(5-6)11-4-3-10-7/h1-5
IUPAC Name
6-chloroquinoxaline
Canonical SMILES
C1=CC2=NC=CN=C2C=C1Cl
InChI Key
HOOMNCITVCXDTR-UHFFFAOYSA-N
Boiling Point
276.9ºC at 760mmHg
Flash Point
147.9ºC
Density
1.349g/cm³
Exact Mass
164.01400
Hazard Statements
Xi
H-Bond Acceptor
2
H-Bond Donor
0

Upstream Synthesis Route 1

  • 6935-29-1
  • 91-19-0
  • 1448-87-9
  • 5448-43-1
  • 7483-33-2

Reference: [1] Tetrahedron, 1989, vol. 45, # 24, p. 7795 - 7804

Upstream Synthesis Route 2

  • 6935-29-1
  • 1448-87-9
  • 5448-43-1
  • 62163-09-1
  • 1196-57-2

Reference: [1] Tetrahedron, 1989, vol. 45, # 24, p. 7795 - 7804

Upstream Synthesis Route 3

  • 6935-29-1
  • 1448-87-9
  • 5448-43-1

Reference: [1] Bulletin des Societes Chimiques Belges, 1986, vol. 95, # 8, p. 663 - 670

Downstream Synthesis Route 1

  • 5448-43-1
  • 39267-11-3
  • 6639-79-8

Reference: [1]Landquist
[Journal of the Chemical Society, 1953, p. 2816,2819]

Downstream Synthesis Route 2

  • 5448-43-1
  • 73855-45-5

Reference: [1]Zhang, Lingjuan; Qiu, Ruiying; Xue, Xiao; Pan, Yixiao; Xu, Conghui; Li, Huanrong; Xu, Lijin
[Advanced Synthesis and Catalysis, 2015, vol. 357, # 16-17, p. 3529 - 3537]

Downstream Synthesis Route 3

  • 5448-43-1
  • 6639-80-1

Reference: [1]Landquist
[Journal of the Chemical Society, 1953, p. 2816,2819]
[2]Landquist
[Journal of the Chemical Society, 1953, p. 2816,2819]

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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