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178373

2′,4′-Dichloroacetophenone

Name: 2′,4′-Dichloroacetophenone
Brand: ALDRICH

96%

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About This Item

Linear Formula:

Cl₂C₆H₃COCH₃

CAS Number:

2234-16-4

Molecular Weight:

189.04

NACRES:

NA.22

PubChem Substance ID:

24850737

UNSPSC Code:

12352100

EC Number:

218-780-8

MDL number:

MFCD00000581

Assay:

96%

Form:

solid

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Properties

Quality Level

100

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

SMILES string

CC(=O)c1ccc(Cl)cc1Cl

InChI

1S/C8H6Cl2O/c1-5(11)7-3-2-6(9)4-8(7)10/h2-4H,1H3

InChI key

XMCRWEBERCXJCH-UHFFFAOYSA-N

Description

Application

2′,4′-Dichloroacetophenone was used in the synthesis of the Schiff base derivatives.

pictograms

GHS05,GHS07

signalword

Danger

hcodes

H302,H318

pcodes

P264 - P270 - P280 - P301 + P312 - P305 + P351 + P338 - P501

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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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)

[Synthesis of a new cyclodextrin derivative and its application as CGC chiral stationary phase in determination of enantiomeric excess].

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

Glutathione-dependent reductive dehalogenation of 2,2',4'-trichloroacetophenone to 2',4'-dichloroacetophenone.

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

Global Trade Item Number

SKU	GTIN
178373-100G	04061838753748
178373-25G	04061838753755