25643-78-1

Basic information

• Product Name: Benzenamine, N-(1,3-dimethyl-2-imidazolidinylidene)-
• CAS NO: 25643-78-1
• Molecular Formula: C11H15N3
• Molecular Weight: 189.26
• Mol File: 25643-78-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-(1,3-dimethyl-2-imidazolidinylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-(1,3-dimethyl-2-imidazolidinylidene)-(25643-78-1)
• EPA Substance Registry System: Benzenamine, N-(1,3-dimethyl-2-imidazolidinylidene)-(25643-78-1)

Safety Data

• Hazardous Substances Data: 25643-78-1(Hazardous Substances Data)

Upstream product

• 103-71-9 phenyl isocyanate 
• 138767-63-2 Dimethyl-[2-(1,2,3-trimethyl-[1,3,2]diazasilolidin-2-yl)-benzyl]-amine 
• 138767-59-6 1,2,5-Trimethyl-2,3-diphenyl-[1,3,5,2]triazasilepane-4-thione 
• 138767-90-5 2-(2-Dimethylaminomethyl-phenyl)-1,2,5-trimethyl-3-phenyl-[1,3,5,2]triazasilepane-4-thione 
• 138767-58-5 2,5,8-Trimethyl-1,2,3-triphenyl-[1,3,5,8,2]tetrazasilonane-4,9-dione 
• 592489-03-7 1,3-dimethyl-2-imidazolidinone O-p-tosyloxime 
• 37091-73-9 2-chloro-1,3-dimethylimidazolinium chloride 
• 62-53-3 aniline 
• 42136-39-0 1,3-dimethyl-2-imidazolidinone oxime 
• 592489-01-5 1,3-dimethyl-2-imidazolidinone O-(tetrahydropyran-2-yl)oxime 
• 103-72-0 phenyl isothiocyanate 
• 56521-11-0 methyl-3 diethyl-2,2 germa-2 oxazolidine-1,3 
• 622-44-6 phenylcarbonimidic dichloride 

Downstream Products

• 100-61-8 N-methylaniline 
• 142-04-1 aniline hydrochloride 

Relevant articles and documents

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Guanidines as a nitrogen source for direct conversion of epoxides to aziridines

Direct conversion of epoxides to aziridines was achieved with guanidines as a nitrogen source. Stereochemical inversion at the chiral centers of epoxides was observed without loss of optical purity.

Aminosilylation of heterocumulenes and the intramolecular decomposition of their silyl-functionalized adducts

Heteroorganic amidosilanes are readily obtained by interaction of CO2, CS2 and other heterocumulenes with pentacoordinated diaminosilanes.A comparison is made with the corresponding reactions of tetracoordinated species.Decompositon of these bifunctional organosilanes gives 2-substituted ureido derivatives and base-stabilized low coordinated silicon species, seemingly by a unimolecular thermal β-elimination.