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357669

Sigma-Aldrich

7-Chloroquinaldine

99%

Synonym(s):

7-Chloro-2-methylquinoline

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About This Item

Empirical Formula (Hill Notation):
C10H8ClN
CAS Number:
4965-33-7
Molecular Weight:
177.63
Beilstein:
115318
MDL number:
MFCD00075436
UNSPSC Code:
12352100
PubChem Substance ID:
24861932
NACRES:
NA.22

Assay

99%

form

solid

mp

74-78 °C (lit.)

functional group

chloro

SMILES string

Cc1ccc2ccc(Cl)cc2n1

InChI

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

InChI key

WQZQFYRSYLXBGP-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - 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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Certificates of Analysis (COA)

Lot/Batch Number
MKCT8743
MKCS5397
MKCP9844
MKCL2393
MKCD7859

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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)
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)
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)

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