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Merck
CN

178373

2′,4′-二氯苯乙酮

96%

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关于此项目

线性分子式:
Cl2C6H3COCH3
化学文摘社编号:
分子量:
189.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-780-8
MDL number:
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产品名称

2′,4′-二氯苯乙酮, 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

Application

2′,4′-二氯苯乙酮用于席夫碱衍生物的合成

pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

存储类别

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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