334251
2-Quinolinecarboxaldehyde
97%
Synonym(s):
2-Formylquinoline, 2-Quinolinecarbaldehyde, 2-Quinolylaldehyde, 2-Quinolylcarbaldehyde
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About This Item
Empirical Formula (Hill Notation):
C10H7NO
CAS Number:
Molecular Weight:
157.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
mp
70-72 °C (lit.)
functional group
aldehyde
SMILES string
[H]C(=O)c1ccc2ccccc2n1
InChI
1S/C10H7NO/c12-7-9-6-5-8-3-1-2-4-10(8)11-9/h1-7H
InChI key
WPYJKGWLDJECQD-UHFFFAOYSA-N
Application
2-Quinolinecarboxaldehyde was used in the preparation of:
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Shengju Ou et al.
Chemical communications (Cambridge, England), (42)(42), 4392-4394 (2006-10-24)
A selective and sensitive fluorescent sensor for detection of Hg2+ in natural water was achieved by incorporating the well-known fluorophore quinoline group and a water-soluble D-glucosamine group within one molecule.
Addressing the unusual reactivity of 2-pyridinecarboxaldehyde and 2-quinolinecarboxaldehyde in base-catalyzed aldol reactions with acetophenone.
Wachter-Jurcsak N, et al.
Tetrahedron Letters, 39(23), 3903-3906 (1998)
Copper (I)-imine complexes: Synthesis and catalytic activity in olefin cyclopropanation
Attilio Ardizzoia G, et al.
Inorgorganica Chimica Acta, 362(10), 3507-3512 (2009)
Ashaparna Mondal et al.
Dalton transactions (Cambridge, England : 2003), 50(3), 979-997 (2020-12-24)
For diagnosing and annihilating cancer in the human body, herein, we have adopted a one pot convenient synthetic protocol to synthesize a library of half sandwich Ru(ii)-p-cymene-N^N complexes under continuous sonication and isolated their regioisomers by preparative thin layer chromatography
Diana Costa et al.
Biomacromolecules, 18(9), 2928-2936 (2017-08-17)
The development of a suitable delivery system and the targeting of intracellular organelles are both essential for the success of drug and gene therapies. The conception of fluorescent ligands, displaying targeting specificity together with low toxicity, is an emerging and
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