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376825

Sigma-Aldrich

2-Chloro-5-(trifluoromethyl)benzaldehyde

98%

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About This Item

Linear Formula:
ClC6H3(CF3)CHO
CAS Number:
Molecular Weight:
208.56
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

liquid

refractive index

n20/D 1.488 (lit.)

bp

42-44 °C/1.5 mmHg (lit.)

density

1.435 g/mL at 25 °C (lit.)

functional group

aldehyde
chloro
fluoro

SMILES string

FC(F)(F)c1ccc(Cl)c(C=O)c1

InChI

1S/C8H4ClF3O/c9-7-2-1-6(8(10,11)12)3-5(7)4-13/h1-4H

InChI key

OZZOJJJYKYKBNH-UHFFFAOYSA-N

Application

2-Chloro-5-(trifluoromethyl)benzaldehyde may be used as reactant in the three-component reaction of 2-halogenated aromatic aldehydes, 1H-benzo[d]imidazol-5-amine and cyclohexane-1,3-diones to afford imidazoquinolinoacridinone derivatives. It may be used in the gas-phase chemical derivatization of poly(tetrafluoroethylene) and poly(ethylene terephthalate) using gas plasma.

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)

192.2 °F - closed cup

Flash Point(C)

89 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Domino synthesis of fused hexacyclic imidazoquinolinoacridinones catalyzed by CuI/l-proline.
Li C, et al.
Tetrahedron, 70(46), 8919-8924 (2014)
Surface chemical derivatization of plasma-treated PET and PTFE.
Markkula TK, et al.
Surface and Interface Analysis : SIA, 34(1), 583-587 (2002)

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