1-(2-Ethylhexyl)-3-pyrroline-2,5-dione

Base Information

Chemical Name:1-(2-Ethylhexyl)-3-pyrroline-2,5-dione
CAS No.:48149-71-9
Molecular Formula:C12H19NO2
Molecular Weight:209.28500
Hs Code.:
Mol file:48149-71-9.mol

Synonyms:N-2-ethylhexylmaleimide;N-(2-ethyl-hexyl)-maleimide;5-(2-ethylhexyl)maleimide;N-(2-Aethyl-hexyl)-maleinimid;N-2-ethylhexyl maleimide;

Suppliers and Price of 1-(2-Ethylhexyl)-3-pyrroline-2,5-dione

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(2-Ethylhexyl)-3-pyrroline-2,5-dione

Chemical Property:

PSA：37.38000
LogP:2.06570

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

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Technology Process of 1-(2-Ethylhexyl)-3-pyrroline-2,5-dione

There total 3 articles about 1-(2-Ethylhexyl)-3-pyrroline-2,5-dione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 108-31-6
maleic anhydride

: 104-75-6
2-Ethylhexylamine

: 48149-71-9
N-(2-ethylhexyl)maleimide

Guidance literature:: maleic anhydride; 2-Ethylhexylamine; In toluene; at 80 ℃;

With 1,1,1,3,3,3-hexamethyl-disilazane; zinc dibromide; In toluene; at 80 ℃; for 2.5h;

Reference yield: 30.0%

: 83701-48-8,6975-33-3
N-(2-ethylhexyl)maleamic acid

: 48149-71-9
N-(2-ethylhexyl)maleimide

Guidance literature:: With sodium acetate; acetic anhydride; at 100 ℃; for 1h;
DOI:10.1002/pola.29421

Reference yield:

: 104-75-6
2-Ethylhexylamine

: 48149-71-9
N-(2-ethylhexyl)maleimide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane

2: sodium acetate; acetic anhydride

With sodium acetate; acetic anhydride; In dichloromethane;
DOI:10.1002/ejoc.201201065