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4829-67-8

4829-67-8 structure

4829-67-8 structure

Name: ethyl 7-chloro-3-oxo-4H-quinoxaline-2-carboxylate
Chemical Name: ethyl 7-chloro-3-oxo-4H-quinoxaline-2-carboxylate
CAS Number: 4829-67-8
Molecular Formula: C₁₁H₉ClN₂O₃
Molecular Weight: 252.65400
Create Date: 2016-10-26 15:54:58
Modify Date: 2024-01-10 12:31:44

Name	ethyl 7-chloro-3-oxo-4H-quinoxaline-2-carboxylate
Synonyms	ETHYL 7-CHLORO-3-OXO-3,4-DIHYDROQUINOXALINE-2-CARBOXYLATE 7-Chlor-3-hydroxy-chinoxalin-2-carbonsaeure-ethylester 7-chloro-3-oxo-3,4-dihydro-quinoxaline-2-carboxylic acid ethyl ester ethyl 7-chloro-3,4-dihydro-3-oxoquinoxaline-2-carboxylate

Molecular Formula	C₁₁H₉ClN₂O₃
Molecular Weight	252.65400
Exact Mass	252.03000
PSA	72.05000
LogP	1.75320

866417-22-3 structure

866417-22-3

~89%

4829-67-8 structure

4829-67-8

Literature: Takano, Yasuo; Shiga, Futoshi; Asano, Jun; Ando, Naoki; Uchiki, Hideharu; Fukuchi, Kazunori; Anraku, Tsuyosi Bioorganic and Medicinal Chemistry, 2005 , vol. 13, # 20 p. 5841 - 5863

143948-68-9 structure

143948-68-9

~%

4829-67-8 structure

4829-67-8

Literature: Takano, Yasuo; Shiga, Futoshi; Asano, Jun; Ando, Naoki; Uchiki, Hideharu; Fukuchi, Kazunori; Anraku, Tsuyosi Bioorganic and Medicinal Chemistry, 2005 , vol. 13, # 20 p. 5841 - 5863

89-63-4 structure

89-63-4

~%

4829-67-8 structure

4829-67-8

Literature: Takano, Yasuo; Shiga, Futoshi; Asano, Jun; Ando, Naoki; Uchiki, Hideharu; Fukuchi, Kazunori; Anraku, Tsuyosi Bioorganic and Medicinal Chemistry, 2005 , vol. 13, # 20 p. 5841 - 5863

59743-08-7 structure

59743-08-7

95-83-0 structure

95-83-0

~35%

4829-67-8 structure

4829-67-8

4017-32-7 structure

4017-32-7

Literature: Sanna, Paolo; Carta, Antonio; Loriga, Mario; Zanetti, Stefania; Sechi, Leonardo Farmaco, 1998 , vol. 53, # 7 p. 455 - 461

95-83-0 structure

95-83-0

609-09-6 structure

609-09-6

~34%

4829-67-8 structure

4829-67-8

4017-32-7 structure

4017-32-7

Literature: Takano, Yasuo; Shiga, Futoshi; Asano, Jun; Ando, Naoki; Uchiki, Hideharu; Fukuchi, Kazunori; Anraku, Tsuyosi Bioorganic and Medicinal Chemistry, 2005 , vol. 13, # 20 p. 5841 - 5863

Precursor 6
866417-22-3 143948-68-9 89-63-4 59743-08-7
95-83-0 609-09-6
DownStream 1
4017-34-9

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