224944
4-(Trifluoromethyl)benzaldehyde
98%
Synonym(s):
α,α,α-Trifluoro-p-tolualdehyde
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€44.50
50 G
€140.00
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10 G
€44.50
50 G
€140.00
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
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Quality Level
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.)
functional group
aldehyde
fluoro
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.
Signal Word
Warning
Hazard Statements
Precautionary 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
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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)
Tetrahedron Letters, 34, 1925-1925 (1993)
Journal of the American Chemical Society, 115, 8570-8570 (1993)
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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