88734-16-1

Basic information

• Product Name: 2-Imidazolidineselone, 1,3-bis(phenylmethyl)-
• CAS NO: 88734-16-1
• Molecular Formula: C17H18N2Se
• Molecular Weight: 329.303
• Mol File: 88734-16-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Imidazolidineselone, 1,3-bis(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Imidazolidineselone, 1,3-bis(phenylmethyl)-(88734-16-1)
• EPA Substance Registry System: 2-Imidazolidineselone, 1,3-bis(phenylmethyl)-(88734-16-1)

Safety Data

• Hazardous Substances Data: 88734-16-1(Hazardous Substances Data)

Upstream product

• 88734-26-3 2,2'-Diselenobis(1,3-dibenzyl-2-imidazolinium)-bis(trifluormethansulfonat) 
• 1771-57-9 bis(1,3-dibenzylimidazolidin-2-ylidene) 

Downstream Products

• 88734-38-7 2,2'-Selenobis(1,3-dibenzyl-2-imidazolinium)-bis(trifluormethansulfonat) 
• 88734-26-3 2,2'-Diselenobis(1,3-dibenzyl-2-imidazolinium)-bis(trifluormethansulfonat) 

Relevant articles and documents

Synthesis and antimicrobial activity of electron rich olefin derived cyclic ureas

Seventeen cyclic ureas containing imidazolidine and benzimidazoline nuclei were synthesised by the reaction of electron-rich olefins with appropriate group 16 elements (O, S, Se, Te). The compounds synthesised were identified by 1H, 13C-NMR, FT-IR and mass spectroscopic techniques and micro analysis. All compounds studied in this work were screened for their in vitro antimicrobial activity against standard strains: Enterococcus faecalis (ATCC 29212), Staphylococcus aureus (ATCC 29213), Escherichia coli (ATCC 25922) and Pseudomonas aeruginosa (ATCC 27853). Eight of the compounds were found effective to inhibit the growth of Gram-positive bacteria (Enterococcus faecalis and Staphylococcus aureus) at MIC values between 25-400 μg/ml. None of the compounds exhibit antimicrobial activity against gram-negative bacteria (Escherichia coli and Pseudmonas aeruginosa) at the concentrations studied (6.25-800 μg/ml).