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Merck
CN

532134

2-Chloro-N-phenylacetamide

97%

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About This Item

Linear Formula:
C6H5NHCOCH2Cl
CAS Number:
Molecular Weight:
169.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-604-0
MDL number:
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Product Name

2-Chloro-N-phenylacetamide, 97%

InChI key

VONWPEXRCLHKRJ-UHFFFAOYSA-N

InChI

1S/C8H8ClNO/c9-6-8(11)10-7-4-2-1-3-5-7/h1-5H,6H2,(H,10,11)

SMILES string

ClCC(=O)Nc1ccccc1

assay

97%

mp

136-139 °C (lit.)

functional group

amide
chloro

Quality Level

Related Categories

Application

2-Chloro-N-phenylacetamide may be used in the preparation of N,N′-(ethane-1,2-diyl)bis(2-(2-oxo-2-(phenylamino)ethoxy)benzamide), an amide podand. It may also be used to prepare phenylacetamide-based Schiff base ligands by reacting with corresponding hydrazones.

General description

2-Chloro-N-phenylacetamide, also known as chloroacetanilide, can be prepared by reacting aniline with chloroacetylchloride in glacial acetic acid. The analysis of its crystal structure shows the presence of N-H...O hydrogen bonds between the molecules.

ppe

dust mask type N95 (US), Eyeshields, Gloves

pictograms

Exclamation mark

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


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J D Vargo
Analytical chemistry, 70(13), 2699-2703 (1998-07-17)
An analytical method is presented which permits qualitative and quantitative analysis of sulfonic acid degradates of three chloroacetanilide herbicides (acetochlor, alachlor, and metolachlor) and one chloroacetamide herbicide (dimethenamid) in groundwater at trace levels with determination by LC/MS/MS. The analytes were
Rajesh Ghangal et al.
Molecular biology reports, 47(4), 2749-2761 (2020-03-19)
Glutathione S-transferases (GSTs) are multifunctional proteins that help in oxidative stress metabolism and detoxification of xenobiotic compounds. Studies pertaining to GST gene family have been undertaken in various plant species, however no information is available with respect to GST genes
Synthesis and Fluorescence Properties of Eu3+, Tb3+ Complexes with Schiff Base Derivatives.
Liu Y, et al.
Journal of Fluorescence, 26(2), 567-576 (2016)
R E Biagini et al.
Analytical and bioanalytical chemistry, 379(3), 368-374 (2004-05-01)
Body burdens from exposures to pesticides may be estimated from urinary analyses of pesticide parent/metabolite concentrations. Pesticide applicators and others are often exposed to numerous unrelated pesticides, either sequentially or simultaneously. Classically, body burdens of pesticides are analyzed using chemical/instrumental
Synthesis and fluorescent properties of europium complexes with amide-type podand ligands of methyl salicylate.
Liu Y, et al.
Research on Chemical Intermediates, 42(2), 425-438 (2016)

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