1131457-31-2

Basic information

• Product Name: 1,5-dibenzylimidazolidin-2-one
• Synonyms: 1,5-dibenzylimidazolidin-2-one
• CAS NO: 1131457-31-2
• Molecular Weight: 266.343
• Mol File: 1131457-31-2.mol

Chemical Properties

• CAS DataBase Reference: 1,5-dibenzylimidazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-dibenzylimidazolidin-2-one(1131457-31-2)
• EPA Substance Registry System: 1,5-dibenzylimidazolidin-2-one(1131457-31-2)

Safety Data

• Hazardous Substances Data: 1131457-31-2(Hazardous Substances Data)

Upstream product

• 65608-73-3 1-allyl-3-benzylurea 
• 98-80-6 phenylboronic acid 
• 128899-99-0 1-amino-2-N-benzylamino-3-phenylpropane 
• 530-62-1 1,1'-carbonyldiimidazole 

Relevant articles and documents

N-Heterocyclic carbene-gold(I)-catalyzed carboheterofunctionalization of alkenes with arylboronic acids

A new approach to the synthesis of pyrrolidine, tetrahydrofuran, and imidazolidin-2-one via N-heterocyclic carbene-gold(I)-catalyzed intramolecular amino- or oxyarylation reactions from a wide variety of alkene substrates such as N-allyl amides, alcohols, carboxylic acids, and ureas in the presence of Selectfluor under mild conditions has been developed.

The direct synthesis of unsymmetrical vicinal diamines from terminal alkynes: A tandem sequential approach for the synthesis of imidazolidinones

The combination of titanium-catalyzed anti-Markovni- kov hydroamination of terminal alkynes with the Strecker reaction is used in the synthesis of unsymmetrical vicinal diamines via the one-pot synthesis of α-cyanoamines. This methodology is further applied to the efficient synthesis of imidazolidinones. An easy-to-use bis(amidate)titanium precatalyst permits efficient approaches to heterocyclic chemistry from terminal alkynes. Georg Thieme Verlag Stuttgart.