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Home > Encyclopedia > N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine

N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine

N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine structure

N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine 

structure
  • CAS No:

    67747-01-7

  • Chemical Name:

    N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine

  • Synonyms:

    1-Propanamine,N-[2-(2,4,6-trichlorophenoxy)ethyl]-;N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine;N-[2-(2,4,6-Trichlorophenoxy)ethyl]propylamine;N-Propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]amine

  • Categories:

    Agrochemicals  >  Pesticide Intermediates

Description

An oral sulfonylurea hypoglycemic agent which stimulates insulin secretion.

N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine Basic Attributes

282.59396

282.59

266-992-4

2922299090

Characteristics

21.3

4.41610

1.26g/cm3

361.1ºC at 760 mmHg

172.2ºC

1.534

Safety Information

NONH for all modes of transport

P301 + P312 + P330

H302-H413

Drug Information

Substances which lower blood glucose levels. (See all compounds classified as Hypoglycemic Agents.)

Diabrezide

N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine Use and Manufacturing

Methods of Manufacturing

The preparation method is to put 2-(2, 4, 6-trichlorophenoxy) ethyl chloride and a proper excess of n-propylamine into the amination kettle, stir and raise the temperature, react to a certain temperature, react for 8-10h, keep the temperature for 1~ 2h, after the reaction, discharge under reduced pressure, destroy the generated amine salt with alkali, recover n-propylamine, wash with water and extract with toluene, the oil layer is distilled under reduced pressure to obtain the finished product. It is also possible to use 2-(2, 4, 6-trichlorophenoxy) ethyl bromide as a raw material to mix with n-propylamine and heat to reflux for 8 hours. After the reaction, the n-propylamine is removed, acidified with hydrochloric acid, and filtered to obtain a white solid as a finished product.

Uses

N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]amine is an intermediate of the fungicide prochloraz.

Computed Properties

Molecular Weight:282.6
XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:281.014097
Monoisotopic Mass:281.014097
Topological Polar Surface Area:21.3
Heavy Atom Count:16
Complexity:182
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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