178373
2′,4′-Dichloroacetophenone
96%
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About This Item
Linear Formula:
Cl2C6H3COCH3
CAS Number:
Molecular Weight:
189.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-780-8
MDL number:
Product Name
2′,4′-Dichloroacetophenone, 96%
InChI key
XMCRWEBERCXJCH-UHFFFAOYSA-N
InChI
1S/C8H6Cl2O/c1-5(11)7-3-2-6(9)4-8(7)10/h2-4H,1H3
SMILES string
CC(=O)c1ccc(Cl)cc1Cl
assay
96%
form
solid
refractive index
n20/D 1.5635 (lit.)
bp
140-150 °C/15 mmHg (lit.)
mp
33-34 °C (lit.)
functional group
chloro
ketone
Quality Level
Related Categories
Application
2′,4′-Dichloroacetophenone was used in the synthesis of the Schiff base derivatives.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Xue-yan Shi et al.
Se pu = Chinese journal of chromatography, 20(1), 34-36 (2003-01-25)
A new cyclodextrin (CD) derivative, 2,6-di-O-benzyl-3-O-valeryl-beta-CD, was synthesized and characterized by 1H NMR and IR. Using the beta-CD derivative as chiral stationary phase of capillary gas chromatography, one chiral column was prepared. On this column, the enantiomeric excesses (e.e.) of
Microwave assisted rapid and efficient synthesis of nitrogen and sulphur containing heterocyclic compounds and their pharmacological evaluation.
Indian J. Chem. B, 45(7), 1762-1762 (2006)
A Brundin et al.
Biochemical pharmacology, 31(23), 3885-3890 (1982-12-01)
alpha-Haloketones are highly reactive compounds, which are known to undergo enzymatic reduction to methyl ketones. The objective of this research was to characterize the enzymes involved in this reaction and to investigate the mechanism of the reaction. 2,2',4'-Trichloroacetophenone was reduced
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