2-Chloro-7-nitroquinoxaline

• CAS: 55686-94-7
• Catalog Number: ACM55686947
• Category: Other Products
• Molecular Weight: 209.59
• Molecular Formula: C₈H₄ClN₃O₂
• Synonyms: 2-CHLORO-7-NITROQUINOXALINE;TIMTEC-BB SBB014258
• IUPAC Name: 2-chloro-7-nitroquinoxaline
• SMILES: C1=CC2=NC=C(N=C2C=C1[N+](=O)[O-])Cl
• InChI Key: DCWHGXURAAYUEC-UHFFFAOYSA-N
• EC Number: 232-531-0
• Exact Mass: 208.99900
• H-Bond Acceptor: 4
• H-Bond Donor: 0

Synthetic Use

Upstream Synthesis Route 1

• 89898-96-4

• 55686-94-7

Reference: [1] Journal of the Brazilian Chemical Society, 2017, vol. 28, # 10, p. 1874 - 1878
[2] Tetrahedron Letters, 1991, vol. 32, # 10, p. 1311 - 1314
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 13, p. 6169 - 6186
[4] Journal of Medicinal Chemistry, 2011, vol. 54, # 13, p. 4508 - 4522

Upstream Synthesis Route 2

• 109541-16-4

• 55686-94-7

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

Upstream Synthesis Route 3

• 1196-57-2

• 55686-94-7

Reference: [1] Journal of Medicinal Chemistry, 2011, vol. 54, # 13, p. 4508 - 4522
[2] Journal of Medicinal Chemistry, 2016, vol. 59, # 13, p. 6169 - 6186
[3] Journal of the Brazilian Chemical Society, 2017, vol. 28, # 10, p. 1874 - 1878

Upstream Synthesis Route 4

• 89898-96-4

• 55686-94-7

Reference: [1]Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan,1959,vol. 79,p. 658
Chem.Abstr.,1959,p. 21979
[2]Justus Liebigs Annalen der Chemie,1953,vol. 579,p. 212,220

Downstream Synthesis Route 1

• 55686-94-7

• 89898-96-4

Reference: [1]Journal of the Chemical Society,1956,p. 26,27
[2]Justus Liebigs Annalen der Chemie,1953,vol. 579,p. 212,220

Downstream Synthesis Route 2

• 67-56-1
• 55686-94-7

• 142396-58-5

Reference: [1]Liebigs Annalen der Chemie,1992,p. 899 - 902

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