C70401
2-Chloroquinoline
99%
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About This Item
Empirical Formula (Hill Notation):
C9H6ClN
CAS Number:
Molecular Weight:
163.60
Beilstein:
112561
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
99%
form
crystals
bp
266-267 °C (lit.)
mp
34-37 °C (lit.)
density
1.23 g/mL at 25 °C (lit.)
SMILES string
Clc1ccc2ccccc2n1
InChI
1S/C9H6ClN/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H
InChI key
OFUFXTHGZWIDDB-UHFFFAOYSA-N
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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)
230.0 °F - closed cup
Flash Point(C)
110 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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S Fetzner et al.
FEMS microbiology letters, 112(2), 151-157 (1993-09-01)
Resting cells of Pseudomonas putida strain 86 were grown on quinoline transformed 2-chloroquinoline to 2-chloro-cis-7,8-dihydro-7,8-dihydroxyquinoline which was not converted further. 7,8-Dioxygenating activity was present when the enzymes of quinoline catabolism were induced. Quinoline-grown cells of strain 86 treated simultaneously with
K Shiva Kumar et al.
Bioorganic & medicinal chemistry, 20(7), 2199-2207 (2012-03-06)
A number of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives were synthesized via AlCl(3)-mediated C-C bond forming reaction between 2-chloroquinoline-3-carbonitrile and various indoles. The methodology does not require any N-protection of the indoles employed and provided the corresponding products in good yields. The molecular structure
D R Boyd et al.
Organic & biomolecular chemistry, 8(5), 1081-1090 (2010-02-19)
A series of enantiopure 2,2'-bipyridines have been synthesised from the corresponding cis-dihydrodiol metabolites of 2-chloroquinolines. Several of the resulting hydroxylated 2,2'-bipyridines were found to be useful chiral ligands for the asymmetric aminolysis of meso-epoxides leading to the formation of enantioenriched
Yubin Ji et al.
Biomedical chromatography : BMC, 34(8), e4845-e4845 (2020-04-09)
An ultra-high performance liquid chromatography tandem mass spectrometry method was developed for determination of homocysteine (HCY) in human plasma. The HCY was derivatized with 2-chloro-1-methylquinolinium tetrafluoroborate and isolated using solid-phase extraction. Derivatization, isolation and detection procedures were optimized. Satisfactory linearity
Amol A Nagargoje et al.
Chemistry & biodiversity, 17(2), e1900624-e1900624 (2019-12-22)
In search for new fungicidal and free radical scavenging agents, we synthesized a focused library of 2-chloroquinoline based monocarbonyl analogs of curcumin (MACs). The synthesized MACs were evaluated for in vitro antifungal and antioxidant activity. The antifungal activity was evaluated against
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