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Merck
CN

357669

7-Chloroquinaldine

99%

Synonym(s):

7-Chloro-2-methylquinoline

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About This Item

Empirical Formula (Hill Notation):
C10H8ClN
CAS Number:
Molecular Weight:
177.63
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
115318
Assay:
99%
Form:
solid
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InChI

1S/C10H8ClN/c1-7-2-3-8-4-5-9(11)6-10(8)12-7/h2-6H,1H3

SMILES string

Cc1ccc2ccc(Cl)cc2n1

InChI key

WQZQFYRSYLXBGP-UHFFFAOYSA-N

assay

99%

form

solid

mp

74-78 °C (lit.)

functional group

chloro

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - 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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Microwave-assisted Preparation of 3-[2-(7-chloro-2-quinolinyl) ethenyl] benzaldehyde.
ZHANG Z, et al.
Chinese Journal of Pharmaceuticals / Chung-kuo i yao kung yeh tsa chih, 2, 012-012 (2010)
Technological Progress in Synthesis of 7-chloroquinaldine as Intermediate of Anti-asthma Drug.
Dong S, et al.
Chemical Industry Times / Hua Gong Shi Kan, 6, 12-12 (2011)
Synthesis of 7-Chloroquinaldine by Skraup Reaction.
LI S, et al.
Journal of Huaihai Institute of Technology (Natural Sciences Edition) / Huai Hai Gong Xue Yuan Xue Bao (Zi Ran Ke Xue Ban ), 3, 012-012 (2007)
Synthesis of unsymmetrical dithioacetals: an efficient synthesis of a novel LTD4 antagonist, L-660,711.
McNamara JM, et al.
The Journal of Organic Chemistry, 54(15), 3718-3721 (1989)

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