76241-97-9

Basic information

• Product Name: ethyl 5,5-dimethyl-2-imino-4-oxo-1-imidazolidinecarboximidate
• CAS NO: 76241-97-9
• Molecular Weight: 198.225
• Mol File: 76241-97-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 5,5-dimethyl-2-imino-4-oxo-1-imidazolidinecarboximidate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 5,5-dimethyl-2-imino-4-oxo-1-imidazolidinecarboximidate(76241-97-9)
• EPA Substance Registry System: ethyl 5,5-dimethyl-2-imino-4-oxo-1-imidazolidinecarboximidate(76241-97-9)

Safety Data

• Hazardous Substances Data: 76241-97-9(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 420-04-2 CYANAMID 
• 57-15-8 1,1,1-trichloro-2-methyl-2-propanol 

Relevant articles and documents

The reactions of ethyl-, vinyl-, and ethynyl(trichloromethyl)carbinols with aqueous amd methanolic potassium hydroxide, thiourea, and cyanamide

The reactions of ethyl(trichloromethyl)carbinol, dimethyl(trichloromethyl)carbinol. (trichloromethyl)vinylcarbinol, ethynyl(trichloromethyl)carbinol, and 1,1,1-trichloro-3-nonyn-2-ol have been studied with the following reagents.Methanolic potassium hydroxide: α-methoxy acids are formed in 70 and 79 percent yields with the ethyl- and vinylcarbinols respectively.Double bond migration to the conjugated position was observed with the vinylcarbinol.Thiourea: substituted 2-imino-4-thiazolidinones are formed in 27 to 66 percent yield with the first three carbinols with double bond migration in the case of the vinylcarbinol.Cyanamide: the saturated carbinols were converted to substituted ethyl 2-imino-4-oxo-1-imidazolidinecarboximidates in 30 to 60 percent yield.Aqueous potassium hydroxide: α-chloro acids were formed from the ethyl- and vinylcarbinols in 23 and 24 percent yields respectively, again with double bond migration in the case of the vinylcarbinol.The results are discussed in terms of the known parallel reactions with phenyl(trichloromethyl)carbinol, and provide information which illustrates the usefulness and defines the limits of certain known synthetic reactions when applied to the alkyl, alkenyl, and alkynyl trichloromethylcarbinols.