|
|
| | Bis(1,3-diphenyl-2-imidazolidinylidene) Basic information |
| Product Name: | Bis(1,3-diphenyl-2-imidazolidinylidene) | | Synonyms: | 2-(1,3-diphenyl-2-imidazolidinylidene)-1,3-diphenyl-imidazolidin;2,2′-bis(1,3-diphenylimidazolidinylidene),98+%;-Bis(1,3-diphenylimidazolidinylidene),98+%;1,1',3,3'-Tetraphenyl-Δ2,2'-biimidazolidine;2-(1,3-Diphenyl-2-imidazolidinylidene)-1,3-diphenylimidazolidine;Δ2,2'-Bi[1,3-diphenylimidazolidine];2-[1,3-di(phenyl)imidazolidin-2-ylidene]-1,3-di(phenyl)imidazolidine;Imidazolidine, 2-(1,3-diphenyl-2-imidazolidinylidene)-1,3-diphenyl- | | CAS: | 2179-89-7 | | MF: | C30H28N4 | | MW: | 444.57 | | EINECS: | | | Product Categories: | | | Mol File: | 2179-89-7.mol |  |
| | Bis(1,3-diphenyl-2-imidazolidinylidene) Chemical Properties |
| | Bis(1,3-diphenyl-2-imidazolidinylidene) Usage And Synthesis |
| Uses | Bis(1,3-diphenyl-2-imidazolidinylidene) is a electron-rich alkene and used for formylation of arenes | | Preparation | Bis(1,3-diphenyl-2-imidazolidinylidene) is prepared from 1,2-dianilinoethane and triethyl orthoformate[1]. | | storage | Bis(1,3-diphenyl-2-imidazolidinylidene) can store under dry nitrogen; reagent that has oxidized may be upgraded by
washing with CH2Cl2. It readily reacts with protic solvents, e.g. MeOH, and hydrolyzes in the presence of weak acid or basic media. | | References | 1. Wanzlick, H.-W. OS 1967, 47, 14. |
| | Bis(1,3-diphenyl-2-imidazolidinylidene) Preparation Products And Raw materials |
|