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Home > Encyclopedia > 2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide

2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide

2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide structure

2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide 

structure
  • CAS No:

    32428-71-0

  • Formula:

    C11H14ClNO

  • Chemical Name:

    2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide

  • Synonyms:

    Acetamide,2-chloro-N-(2-ethyl-6-methylphenyl)-;o-Acetotoluidide,2-chloro-6′-ethyl-;2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide;2-Chloro-2′-ethyl-6′-methylacetanilide;2′-Ethyl-6′-methyl-2-chloroacetanilide;2′-Methyl-6′-ethyl-α-chloroacetanilide;CGA 13656;N-(Chloroacetyl)-2-ethyl-6-methylaniline;CMEPA

  • Categories:

    Agrochemicals  >  Pesticide Intermediates

Description

N-(2-ethyl-6-methylphenyl)-2-chloroacetamide is an aromatic amide obtained by formal condensation of the carboxy group of chloroacetic acid with the amnio group of 2-ethyl-6-methylaniline. It is an aromatic amide and an organochlorine compound. It derives from a chloroacetic acid.

2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide Basic Attributes

211.68796

211.69

DTXSID60186172

2924299090

Characteristics

29.1

2

1.156g/cm3

120-121 °C @ Solvent: Ethanol, 50%

343.1°C at 760 mmHg

161.3ºC

1.566

Safety Information

P264, P280, P305+P351+P338, P33, P313

H319

Drug Information

2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide is a known human metabolite of Acetachlor.

2-Chloro-N-(2-ethyl-6-methylphenyl)acetamide Use and Manufacturing

Methods of Manufacturing

The preparation method is to add xylene and chloroacetic acid into the reaction kettle, heat to dissolve and move to another reaction kettle, add 2-methyl-6-ethylaniline, stir and mix well, add phosphorus trichloride dropwise, and warm up React, add water, stand still for separation, the phosphorous acid waste liquid is sent to the three wastes for treatment, the material liquid is transferred to the crystallization kettle for crystallization, and the product is filtered.

Uses

N-(2-methyl-6-ethyl)phenylchloroacetamide is an intermediate of the herbicides acetochlor, metolachlor, and meprochlor.

Computed Properties

Molecular Weight:211.69
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:211.0763918
Monoisotopic Mass:211.0763918
Topological Polar Surface Area:29.1
Heavy Atom Count:14
Complexity:196
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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