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Key Documents

150231

Sigma-Aldrich

4-Chloroquinaldine

99%

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About This Item

Empirical Formula (Hill Notation):
C10H8ClN
CAS Number:
Molecular Weight:
177.63
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.622 (lit.)

bp

269-270 °C (lit.)

density

0.881 g/mL at 25 °C (lit.)

functional group

chloro

SMILES string

Cc1cc(Cl)c2ccccc2n1

InChI

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

InChI key

HQAIROMRVBVWSK-UHFFFAOYSA-N

Application

4-Chloroquinaldine was used in the preparation of 4-phenyl-hydrazinoquinaldine.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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208. The reaction between phenylhydrazine and 4-chloroquinoline derivatives, and the preparation of the corresponding 4-benzeneazo-and 4-amino-compounds.
Backeberg OG.
Journal of the Chemical Society, 1083-1087 (1938)
K N Vennila et al.
Bioorganic chemistry, 81, 184-190 (2018-08-24)
The induced fit docking of anilino quinoline scaffold results in the required hydrogen bonding interactions with amino acid residues in the orthosteric site of 3 Phosphoinositide dependent kinase (PDK1). The rational design of 4-substituted amino quinolines is carried out and

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