ChemicalBook Product Catalog Pharmaceutical intermediates Heterocyclic compound Quinoline compounds ISOQUINOLINE N-OXIDE

ISOQUINOLINE N-OXIDE

ISOQUINOLINE N-OXIDE Basic information
Product Name:ISOQUINOLINE N-OXIDE
Synonyms:Isoquinoline oxide;isoquinoline-oxide;ISOQUINOLINE 2-OXIDE;ISOQUINOLINE N-OXIDE;ISOQUINOLIN-N-OXIDE;ISOQUINOLINE N-OXIDE: 50% W/V IN WATER;Isoquinoline N-oxide, min 50% w/v in water;2-Oxylatoisoquinoline-2-ium
CAS:1532-72-5
MF:C9H7NO
MW:145.16
EINECS:216-242-7
Product Categories:Building Blocks;Heterocyclic Building Blocks;Isoquinolines
Mol File:1532-72-5.mol
ISOQUINOLINE N-OXIDE Structure
ISOQUINOLINE N-OXIDE Chemical Properties
Melting point 103-105 °C(lit.)
Boiling point 170°C 3mm
density 1.1555 (rough estimate)
refractive index 1.4500 (estimate)
Fp 170°C/3mm
storage temp. Inert atmosphere,Room Temperature
pka0.74±0.30(Predicted)
form powder to crystal
color Light yellow to Yellow to Orange
Sensitive Hygroscopic
BRN 114345
InChIKeyRZIAABRFQASVSW-UHFFFAOYSA-N
CAS DataBase Reference1532-72-5(CAS DataBase Reference)
Safety Information
Risk Statements 36/38
Safety Statements 24/25
WGK Germany 3
HS Code 2933499090
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
ISOQUINOLINE N-OXIDE Usage And Synthesis
Chemical Propertiescream to brown powder or chunks
UsesIsoquinoline n-oxide an isoquinoline metabolite.
DefinitionChEBI: Isoquinoline N-oxide is a member of isoquinolines.
Synthesis Reference(s)Tetrahedron, 50, p. 12185, 1994 DOI: 10.1016/S0040-4020(01)89569-7
General DescriptionPhotochemical isomerization of isoquinoline N-oxide in methanol or water has been investigated by steady-light irradiation and flash spectroscopy. It is a useful intermediate for isoquinoline derivatives. It causes the oxidation of fullerene C60 under ultrasonic irradiation in air.
ISOQUINOLINE N-OXIDE Preparation Products And Raw materials
Raw materialsAcetic acid-->Hydrogen peroxide-->Isoquinoline
Preparation ProductsIsoquinolin-4-ol-->1-Bromoisoquinoline-->2-(ISOQUINOLIN-1-YL)ACETIC ACID
1-nitro-6-azabenzo(a)pyrene N-oxide (6aR)-4,5,6,6a,7,8-Hexahydro-1-hydroxy-2,10,11,12-tetramethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline 6-oxide 5-[[p-(Dimethylamino)phenyl]azo]isoquinoline 2-oxide 7-METHOXYISOQUINOLINE 2-OXIDE Thieno[2,3-c]isoquinoline 1-oxide ISOQUINOLINE N-OXIDE 3-CHLOROISOQUINOLINE 2-OXIDE 5-NITROISOQUINOLINE-N-OXIDE 7-Bromoisoquinoline-N-oxide 3-nitro-6-azabenzo(a)pyrene N-oxide 5/7-Bromoisoquinoline 2-oxides (6aR)-4,5,6,6a,7,8-Hexahydro-1,2,10,11,12-pentamethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline 6-oxide 3-METHYLISOQUINOLINE 2-OXIDE 4-BROMO-ISOQUINOLINE 2-OXIDE (6aR)-4,5,6,6a,7,8-Hexahydro-1,10-dihydroxy-2,11,12-trimethoxy-6-methylbenzo[6,7]cyclohept[1,2,3-ij]isoquinoline 6-oxide THIENO[2,3-C]ISOQUINOLINE 4-OXIDE Thieno[3,4-c]isoquinoline 1-oxide 7,8-Dihydro-1,3-dioxolo[4,5-g]isoquinoline 6-oxide
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