1-(But-3-enyl)-pyrrolidine-2,5-dione

Base Information

Chemical Name:1-(But-3-enyl)-pyrrolidine-2,5-dione
CAS No.:58805-10-0
Molecular Formula:C8H11NO2
Molecular Weight:153.181
Hs Code.:
DSSTox Substance ID:DTXSID90496211
Nikkaji Number:J901.517E
Wikidata:Q82344922
Mol file:58805-10-0.mol

Synonyms:1-but-3-enylpyrrolidine-2,5-dione;58805-10-0;1-(but-3-enyl)-pyrrolidine-2,5-dione;SCHEMBL19277204;DTXSID90496211;1-(But-3-en-1-yl)pyrrolidine-2,5-dione

Suppliers and Price of 1-(But-3-enyl)-pyrrolidine-2,5-dione

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1-(But-3-enyl)-pyrrolidine-2,5-dione

Chemical Property:

PSA：37.38000
LogP:0.64940
XLogP3:0.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:153.078978594
Heavy Atom Count:11
Complexity:182

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCCN1C(=O)CCC1=O

Technology Process of 1-(But-3-enyl)-pyrrolidine-2,5-dione

There total 5 articles about 1-(But-3-enyl)-pyrrolidine-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: 99.5%

: 123-56-8,89963-74-6
Succinimide

: 5162-44-7
1-bromo-4-butene

: 58805-10-0
N-(3-butenyl)succinimide

Guidance literature:: With 18-crown-6 ether; potassium carbonate; In toluene; for 16h; Heating;

Reference yield: 96.0%

: 123-56-8,89963-74-6
Succinimide

: 627-27-0
homoalylic alcohol

: 58805-10-0
N-(3-butenyl)succinimide

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; for 3h; Ambient temperature;
DOI:10.1021/ja00338a033