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348074

Sigma-Aldrich

2-Chloro-4-fluorobenzaldehyde

97%

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Linear Formula:
ClC6H3(F)CHO
CAS Number:
84194-36-5
Molecular Weight:
158.56
MDL number:
MFCD00042527
PubChem Substance ID:
24861548
NACRES:
NA.22

Quality Level

100

Assay

97%

form

solid

bp

118-120 °C/50 mmHg (lit.)

mp

60-63 °C (lit.)

SMILES string

Fc1ccc(C=O)c(Cl)c1

InChI

1S/C7H4ClFO/c8-7-3-6(9)2-1-5(7)4-10/h1-4H

InChI key

KMQWNQKESAHDKD-UHFFFAOYSA-N

Related Categories

General description

2-Chloro-4-fluorobenzaldehyde is a halogen substituted benzaldehyde.

Application

2-Chloro-4-fluorobenzaldehyde may be used in the synthesis of substituted α-cyanocinnamic acid, via Knoevenagel condensation reaction. It may be used in the synthesis of 2-(2-benzimidazolyl)-3-(2-chloro-4-fluorophenyl)acrylonitrile.

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

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Biological activity and DNA binding studies of 2-substituted benzimidazo [1, 2-a] quinolines bearing different amino side chains.
Perin N, et al.
MedChemComm, 4(12), 1537-1550 (2013)
Thorsten W Jaskolla et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(34), 12200-12205 (2008-08-30)
Matrix-assisted laser desorption ionization (MALDI) has become an enabling technology for the fields of protein mass spectrometry (MS) and proteomics. Despite its widespread use, for example, in protein identification via peptide mass fingerprinting, a comprehensive model for the generation of

Articles

Knoevenagel Condensation Reaction

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

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