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C70401

Sigma-Aldrich

2-Chloroquinoline

99%

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About This Item

Empirical Formula (Hill Notation):
C9H6ClN
CAS Number:
612-62-4
Molecular Weight:
163.60
Beilstein:
112561
EC Number:
210-317-8
MDL number:
MFCD00006741
UNSPSC Code:
12352100
PubChem Substance ID:
24892924
NACRES:
NA.22

Quality Level

100

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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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

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Certificates of Analysis (COA)

Lot/Batch Number
0000258191
0000192336
0000183607
0000189528
0000188031

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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
Santosh Kumar et al.
International journal of biological macromolecules, 49(3), 356-361 (2011-06-07)
This paper describes an elegant cross-linking technique for the preparation of chitosan-chloroquinoline derivative by using a greener technique. Chitosan solution in aqueous acetic acid was treated with 2-chloroquinoline-3-carbaldehyde solution to form hydrogel; the resulting hydrogel was subjected to solvent exchange.
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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