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Merck
CN

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)
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InChI

1S/C10H6N2O/c11-6-8-5-4-7-2-1-3-9(13)10(7)12-8/h1-5,13H

SMILES string

Oc1cccc2ccc(nc12)C#N

InChI key

KUQKKIBQVSFDHX-UHFFFAOYSA-N

assay

≥98.0% (GC)

functional group

nitrile

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

pictograms

Exclamation mark

signalword

Warning

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

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