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Merck
CN

348074

2-氯-4-氟苯甲醛

97%

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线性分子式:
ClC6H3(F)CHO
化学文摘社编号:
分子量:
158.56
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

2-氯-4-氟苯甲醛, 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

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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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

商品

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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