Isoquinoline N-oxide - CAS 1532-72-5
Catalog: |
BB010873 |
Product Name: |
Isoquinoline N-oxide |
CAS: |
1532-72-5 |
Synonyms: |
2-oxidoisoquinolin-2-ium |
IUPAC Name: | 2-oxidoisoquinolin-2-ium |
Description: | Isoquinoline n-oxide an isoquinoline metabolite. |
Molecular Weight: | 145.16 |
Molecular Formula: | C9H7NO |
Canonical SMILES: | C1=CC=C2C=[N+](C=CC2=C1)[O-] |
InChI: | InChI=1S/C9H7NO/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H |
InChI Key: | RZIAABRFQASVSW-UHFFFAOYSA-N |
Boiling Point: | 170 °C / 3 mmHg |
Density: | 1.13 g/cm3 |
MDL: | MFCD00006903 |
LogP: | 2.26830 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112574107-A | Synthesis method of atropisomeric 1-arylisoquinoline N-oxide and derivatives thereof | 20201218 |
WO-2021202914-A1 | Separation of rare earth elements | 20200402 |
WO-2021138298-A1 | Malt1 modulators and uses thereof | 20191230 |
WO-2021115432-A1 | Novel quinazoline-containing compound, and intermediate thereof and use thereof | 20191211 |
CN-110256342-A | A kind of synthetic method of 2- cyano-quinoline derivatives | 20190716 |
PMID | Publication Date | Title | Journal |
22274290 | 20120501 | Generation of diverse 1-imidazolylisoquinolines via silver triflate-catalyzed reaction of 2-alkynylbenzaldoxime with imidazole | Molecular diversity |
22180132 | 20120206 | Nickel-catalyzed cyclization of ortho-iodoketoximes and ortho-iodoketimines with alkynes: synthesis of highly substituted isoquinolines and isoquinolinium salts | Chemistry, an Asian journal |
18341275 | 20080416 | On the mechanism of asymmetric allylation of aldehydes with allyltrichlorosilanes catalyzed by QUINOX, a chiral isoquinoline N-oxide | Journal of the American Chemical Society |
15857133 | 20050505 | Calculating virtual log P in the alkane/water system (log P(N)(alk)) and its derived parameters deltalog P(N)(oct-alk) and log D(pH)(alk) | Journal of medicinal chemistry |
15047355 | 20040401 | The oxidation of fullerene[C60] with various amine N-oxides under ultrasonic irradiation | Ultrasonics |
Complexity: | 138 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 145.052763847 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 145.052763847 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 25.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.3 |
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Related Functional Groups
Quinoline/Isoquinoline
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