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Merck
CN

348074

2-Chloro-4-fluorobenzaldehyde

97%

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About This Item

Linear Formula:
ClC6H3(F)CHO
CAS Number:
84194-36-5
Molecular Weight:
158.56
NACRES:
NA.22
PubChem Substance ID:
24861548
UNSPSC Code:
12352100
MDL number:
MFCD00042527

Key Documents

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Product Name

2-Chloro-4-fluorobenzaldehyde, 97%

InChI

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

SMILES string

Fc1ccc(C=O)c(Cl)c1

InChI key

KMQWNQKESAHDKD-UHFFFAOYSA-N

assay

97%

form

solid

bp

118-120 °C/50 mmHg (lit.)

mp

60-63 °C (lit.)

functional group

aldehyde
chloro
fluoro

Quality Level

100

Related Categories

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.

General description

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM3754
MKCK3916
MKCF1747
MKCB0381V
MKBS0478V

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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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