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224944

Sigma-Aldrich

4-(Trifluoromethyl)benzaldehyde

98%

Synonym(s):

α,α,α-Trifluoro-p-tolualdehyde

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About This Item

Linear Formula:
CF3C6H4CHO
CAS Number:
Molecular Weight:
174.12
Beilstein:
1101680
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.463 (lit.)

bp

66-67 °C/13 mmHg (lit.)

density

1.275 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)c1ccc(cc1)C(F)(F)F

InChI

1S/C8H5F3O/c9-8(10,11)7-3-1-6(5-12)2-4-7/h1-5H

InChI key

BEOBZEOPTQQELP-UHFFFAOYSA-N

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Application


  • Correlation data of (Z)-1-thiosemicarbazide via spectroscopic methods and Density Functional Theory studies: Synthesis of (Z)-1-[4-(trifluoromethyl)benzylidene]thiosemicarbazide using 4-(trifluoromethyl)benzaldehyde in ethanol (UM Osman et al., 2019).

  • Transition-Metal-Free Trifluoromethylation of Aldehyde Derivatives with Sodium Trifluoromethanesulfinate: Investigates the direct C-H trifluoromethylation of benzaldehyde and other synthetic equivalents (Z Tan et al., 2017).

Other Notes

May form precipitate upon standing which does not affect use. Warm gently to redissolve solid.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Tetrahedron, 49, 9613-9613 (1993)
Synthesis and properties of new pyridine-bridged poly (ether-imide) s based on 4-(4-trifluoromethylphenyl)-2, 6-bis [4-(4-aminophenoxy) phenyl] pyridine.
Journal of Fluorine Chemistry, 129(1), 56-63 (2008)
Journal of the American Chemical Society, 115, 8570-8570 (1993)
Tetrahedron Asymmetry, 5, 411-411 (1994)
Peng Cao et al.
The Journal of organic chemistry, 72(17), 6628-6630 (2007-07-28)
In the presence of sodium hydrosulfite and a catalytic amount of AsPh3 and Fe(TCP)Cl, aldehydes react with ethyl diazoacetate to give the corresponding alpha,beta-unsaturated esters in high yields with excellent stereoselectivities (E/Z > 50/1).

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