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Sigma-Aldrich

2,4,5-Trifluorobenzaldehyde

97%

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About This Item

Linear Formula:
F3C6H2CHO
CAS Number:
165047-24-5
Molecular Weight:
160.09
MDL number:
MFCD00061196
UNSPSC Code:
12352100
PubChem Substance ID:
24877658
NACRES:
NA.22

Quality Level

100

assay

97%

refractive index

n20/D 1.482 (lit.)

bp

168 °C (lit.)

density

1.408 g/mL at 25 °C (lit.)

SMILES string

Fc1cc(F)c(C=O)cc1F

InChI

1S/C7H3F3O/c8-5-2-7(10)6(9)1-4(5)3-11/h1-3H

InChI key

CYIFJRXFYSUBFW-UHFFFAOYSA-N

Related Categories

Application

2,4,5-Trifluorobenzaldehyde may be used in the synthesis of:
  • bis(2,4,5-trifluorophenyl)methanone
  • 8-phenyl-7-tosyl-1-(2,4,5-trifluorophenyl)octahydro-1H-pyrano[3,4-c] pyridine
  • (E)-4-methoxy-N′-(2,4,5-trifluorobenzylidene)-benzohydrazide monohydrate

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

138.2 °F - closed cup

flash_point_c

59 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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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Aminol initiated Prins cyclization for the synthesis of octahydro-1H-pyrano [3, 4-c] pyridine and hexahydro-1H-furo [3, 4-c] pyrrole derivatives.
Tetrahedron Letters, 55(34), 4817-4821 (2014)
Zachary R Woydziak et al.
The Journal of organic chemistry, 77(1), 473-481 (2011-11-25)
Fluorination of fluorophores can substantially enhance their photostability and improve spectroscopic properties. To facilitate access to fluorinated fluorophores, bis(2,4,5-trifluorophenyl)methanone was synthesized by treatment of 2,4,5-trifluorobenzaldehyde with a Grignard reagent derived from 1-bromo-2,4,5-trifluorobenzene, followed by oxidation of the resulting benzyl alcohol.
Zachary R Woydziak et al.
Synthesis, 46(2), 158-164 (2014-06-11)
Fluorinated fluorophores are valuable tools for studies of biological systems. However, amine-reactive single-isomer derivatives of these compounds are often very expensive. To provide an inexpensive alternative, we report a practical synthesis of 4-carboxy-Pennsylvania Green methyl ester. Derivatives of this hydrophobic
(E)-4-Methoxy-N'-(2, 4, 5-trifluorobenzylidene) benzohydrazide monohydrate.
Maheswari R, et al.
IUCrJ, 1(5), x160846-x160846 (2016)

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