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Sigma-Aldrich

2,3,5,6-Tetrafluorobenzaldehyde

97%

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About This Item

Linear Formula:
HC6F4CHO
CAS Number:
19842-76-3
Molecular Weight:
178.08
MDL number:
MFCD00167387
UNSPSC Code:
12352100
PubChem Substance ID:
24859757
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.469 (lit.)

bp

178 °C (lit.)

density

1.525 g/mL at 25 °C (lit.)

functional group

aldehyde
fluoro

SMILES string

Fc1cc(F)c(F)c(C=O)c1F

InChI

1S/C7H2F4O/c8-4-1-5(9)7(11)3(2-12)6(4)10/h1-2H

InChI key

YIRYOMXPMOLQSO-UHFFFAOYSA-N

Related Categories

General description

2,3,5,6-Tetrafluorobenzaldehyde is a polysubstituted benzaldehyde and was evaluated as a substrate of PmHNL (Prunus mume hydroxynitrile lyase). Reaction of 2,3,5,6-tetrafluorobenzaldehyde with dipyrromethane was reported.

Application

2,3,5,6-Tetrafluorobenzaldehyde was used in the preparation of 1,3-bis(2,4,6-trimethylphenyl)-2-(2,3,5,6-tetrafluorophenyl)imidazolidine and 1,3-dimethyl-2-(2,3,5,6-tetrafluorophenyl)imidazolidine.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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)

165.2 °F - closed cup

Flash Point(C)

74 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8954
STBJ7008
STBJ2142
STBH0153
STBG0531V

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A new (R)-hydroxynitrile lyase from< i> Prunus mume</i>: asymmetric synthesis of cyanohydrins.
Nanda S, et al.
Tetrahedron, 61(46), 10908-10916 (2005)
Effects of aldehyde or dipyrromethane substituents on the reaction course leading to meso-substituted porphyrins.
Geier III, et al.
Tetrahedron, 60(50), 11435-11444 (2004)
Gregory W Nyce et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 10(16), 4073-4079 (2004-08-19)
The synthesis of N-heterocyclic carbene (NHC) adducts by condensation of diamines with appropriately substituted benzaldehydes is described. This simplified approach provides the NHC adduct without first having to generate the carbene followed by its protection. These adducts undergo thermal deprotection

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