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ChemicalBook--->CAS DataBase List--->3565-26-2

3565-26-2

3565-26-2 Structure

3565-26-2 Structure
IdentificationMore
[Name]

5-NITROSO-8-HYDROXYQUINOLINE
[CAS]

3565-26-2
[Synonyms]

5-NITROSO-8-HYDROXYQUINOLINE
5-NITROSO-8-QUINOLINOL
5-NITROSO-OXINE
8-HYDROXY-5-NITROQUINOLINE
8-HYDROXY-5-NITROSOQUINOLINE
NSC 3852
5-Nitroso-8-cinnolinol
5-nitroso-8-quinolino
8-Quinolinol, 5-nitroso-
Hydron III
hydroniii
RMH-79
5-nitrosoquinolin-8-ol
5-NITROSO-8-HYDROXYQUINOLINE 95+%
[EINECS(EC#)]

222-650-6
[Molecular Formula]

C9H6N2O2
[MDL Number]

MFCD00041862
[Molecular Weight]

174.16
[MOL File]

3565-26-2.mol
Chemical PropertiesBack Directory
[Appearance]

slightly yellow to yellow-green powder
[Melting point ]

245 °C
[Boiling point ]

305.12°C (rough estimate)
[density ]

1.40
[refractive index ]

1.5651 (estimate)
[storage temp. ]

Store at RT
[solubility ]

insoluble in EtOH; insoluble in H2O; ≥7.35 mg/mL in DMSO
[form ]

solid
[color ]

Needles from EtOH
[CAS DataBase Reference]

3565-26-2(CAS DataBase Reference)
[EPA Substance Registry System]

8-Quinolinol, 5-nitroso- (3565-26-2)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R5:Heating may cause an explosion.
R40:Limited evidence of a carcinogenic effect.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S36/37:Wear suitable protective clothing and gloves .
[Toxicity]

mmo-sat 1 mmol/plate MUREAV 164,263,86
Hazard InformationBack Directory
[Chemical Properties]

slightly yellow to yellow-green powder
[Uses]

5-NITROSO-8-HYDROXYQUINOLINE is shown to have cell differentiation and antiproliferative activity in human breast cancer cells in tissue culture and antitumor activity in mice bearing P388 and L1210 leukemic cells.
[Definition]

ChEBI: 5-nitroso-8-quinolinol is a hydroxyquinoline.
[Biological Activity]

Histone deacetylase inhibitor. Causes cell differentiation and antiproliferative activity in MCF-7 human breast cancer cells in vitro and displays antitumor activity in vivo .
[Safety Profile]

Poison by intravenous and intraperitoneal routes. Many nitroso compounds are carcinogens. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
[storage]

Store at RT
[References]

[1]. martirosyan a, leonard s, shi x, et al. actions of a histone deacetylase inhibitor nsc3852 (5-nitroso-8-quinolinol) link reactive oxygen species to cell differentiation and apoptosis in mcf-7 human mammary tumor cells. j pharmacol exp ther, 2006, 317(2): 546-552.
[2]. strobl js, seibert cw, li y, et al. inhibition of toxoplasma gondii and plasmodium falciparum infections in vitro by nsc3852, a redox active antiproliferative and tumor cell differentiation agent. j parasitol, 2009, 95(1): 215-223.
Spectrum DetailBack Directory
[Spectrum Detail]

5-NITROSO-8-HYDROXYQUINOLINE(3565-26-2)MS
5-NITROSO-8-HYDROXYQUINOLINE(3565-26-2)IR1
5-NITROSO-8-HYDROXYQUINOLINE(3565-26-2)IR2
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