55087
8-Hydroxy-2-quinolinecarbonitrile
≥98.0% (GC)
Synonym(s):
8-Hydroxyquinaldonitrile
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About This Item
Empirical Formula (Hill Notation):
C10H6N2O
CAS Number:
Molecular Weight:
170.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
473250
Assay:
≥98.0% (GC)
assay
≥98.0% (GC)
functional group
nitrile
SMILES string
Oc1cccc2ccc(nc12)C#N
InChI
1S/C10H6N2O/c11-6-8-5-4-7-2-1-3-9(13)10(7)12-8/h1-5,13H
InChI key
KUQKKIBQVSFDHX-UHFFFAOYSA-N
Application
8-Hydroxy-2-quinolinecarbonitrile may be used in the preparation of 8-hydroxy-2-quinolinemethylamine, a reagent to generate peptoid oligomers.
Other Notes
Building block for preparing chelating agents
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Heterocyclic amines for the construction of peptoid oligomers bearing multi-dentate ligands.
Maayan G, et al.
Tetrahedron Letters, 49(2), 335-338 (2008)
C. Moberg et al.
Journal of the Chemical Society. Chemical Communications, 810-810 (1988)
Vladimir Majerciak et al.
Journal of virology, 93(2) (2018-10-26)
Epstein-Barr virus (EBV) is a ubiquitous human pathogen associated with Burkitt's lymphoma and nasopharyngeal carcinoma. Although the EBV genome harbors more than a hundred genes, a full transcription map with EBV polyadenylation profiles remains unknown. To elucidate the 3' ends
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 55087-1G-F | 04061832577036 |