N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine
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N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine
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CAS No:
67747-01-7
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Chemical Name:
N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine
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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
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CAS No:
N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine Basic Attributes
282.59396
282.59
266-992-4
2922299090
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
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.
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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N-[2-(2,4,6-Trichlorophenoxy)ethyl]-1-propanamine
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