Recommended Products
Quality Level
Assay
97%
form
solid
bp
118-120 °C/50 mmHg (lit.)
mp
60-63 °C (lit.)
functional group
aldehyde
chloro
fluoro
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
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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Biological activity and DNA binding studies of 2-substituted benzimidazo [1, 2-a] quinolines bearing different amino side chains.
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Articles
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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