CAS No.14161-11-6,Pyridazine,3,4,5-trichloro- Suppliers

Detail of "14161-11-6"

CAS Number:

14161-11-6

Name:

Superlist Name:

Molecular Structure:

Formula:

C₄HCl₃N₂

Molecular Weight:

183.42

Synonyms:

NSC 75074;

EINECS:

238-006-2

Density:

1.641 g/cm³

Boiling Point:

322.8 °C at 760 mmHg

Flash Point:

178.7 °C

Hazard Symbols:

Transport Information:

UN 1759

Synthesis and pharmacological study of 10H-pyridazino[4,5-b][1,4]benzoxazines (2,3-diazaphenoxazines): Synthesis and pharmacological study of 10H-pyridazino[4,5-b][1,4]benzoxazines (2,3-diazaphenoxazines). Synthesis of 1 and 1,10-substituted 2,3-diazaphenoxazines. Gortinskaya, T. V.; Nyrkova, V. G.; Savitskaya, N. V.; Fedorova, I. N.; Polezhaeva, A. I.; Mashkovskii, M. D.; Vlasova, T. F. (Vses. Nauchno-Issled. Khim.-Farm. Inst.Several substances like 14161-11-6 may be metioned in this study. im. Ordzhonikidze, Moscow, USSR). 14161-11-6 is also in the experiment. Khim.-Farm. Zh., 11(8), 27-33 (Russian) 1977. CODEN: KHFZAN. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 1 Pyridazinobenzoxazines I [R = H, Me, Et, Bu, PhCH2, (CH2)3NMe2, R1 = Cl] were obtained in 23-38.4% yields by cyclocondensation of an aminophenol with 3,4,5-trichloropyridazine. Subsequent amination and alkoxylation reactions gave 60-76.5% I [R = Me, (CH2)3NMe2, R1 = 4-methyl-1-piperaziinyl, OCH2CH2NEt2, OBu, OEt, 1-pyrrolidinyl, morpholino]. I [R = (CH2)3NMe2, R1 = Cl, OBu; R = Me, R1 = 4-methyl-1-piperazinyl, OBu] showed significant antipyretic and antidepressant activity. ..

Synthesis and pharmacological study of 10H-pyridazino[4,5-b][1,4]benzoxazines (2,3-diazaphenoxazines): Synthesis and pharmacological study of 10H-pyridazino[4,5-b][1,4]benzoxazines (2,3-diazaphenoxazines). Synthesis of 1 and 1,10-substituted 2,3-diazaphenoxazines. Gortinskaya, T. V.; Nyrkova, V. G.; Savitskaya, N. V.; Fedorova, I. N.; Polezhaeva, A. I.; Mashkovskii, M. D.; Vlasova, T. F. (Vses. Nauchno-Issled. Khim.-Farm. Inst.Several substances like 14161-11-6 may be metioned in this study. im. Ordzhonikidze, Moscow, USSR). 14161-11-6 is also in the experiment. Khim.-Farm. Zh., 11(8), 27-33 (Russian) 1977. CODEN: KHFZAN. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 1 Pyridazinobenzoxazines I [R = H, Me, Et, Bu, PhCH2, (CH2)3NMe2, R1 = Cl] were obtained in 23-38.4% yields by cyclocondensation of an aminophenol with 3,4,5-trichloropyridazine. Subsequent amination and alkoxylation reactions gave 60-76.5% I [R = Me, (CH2)3NMe2, R1 = 4-methyl-1-piperaziinyl, OCH2CH2NEt2, OBu, OEt, 1-pyrrolidinyl, morpholino]. I [R = (CH2)3NMe2, R1 = Cl, OBu; R = Me, R1 = 4-methyl-1-piperazinyl, OBu] showed significant antipyretic and antidepressant activity. ..

Detail of "14161-11-6"