1404074-26-5

Basic information

• Product Name: N-((4-(-2-benzoyl-3-methylguanidino)butyl)-1-methyl-5-oxoimidazolidin-2-ylidene)benzamide
• Synonyms: N-((4-(-2-benzoyl-3-methylguanidino)butyl)-1-methyl-5-oxoimidazolidin-2-ylidene)benzamide
• CAS NO: 1404074-26-5
• Molecular Weight: 448.525
• Mol File: 1404074-26-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-((4-(-2-benzoyl-3-methylguanidino)butyl)-1-methyl-5-oxoimidazolidin-2-ylidene)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-((4-(-2-benzoyl-3-methylguanidino)butyl)-1-methyl-5-oxoimidazolidin-2-ylidene)benzamide(1404074-26-5)
• EPA Substance Registry System: N-((4-(-2-benzoyl-3-methylguanidino)butyl)-1-methyl-5-oxoimidazolidin-2-ylidene)benzamide(1404074-26-5)

Safety Data

• Hazardous Substances Data: 1404074-26-5(Hazardous Substances Data)

Upstream product

• 13829-13-5 N-benzoyl-N-methylcyanamide 
• 13515-95-2 L-lysine methyl ester hydrochloride 

Relevant articles and documents

Rearrangements of N-acyl isothioureas. alternate access to acylguanidines from cyanamides

We report a tin-free one-pot radical approach to the synthesis of N-acyl isothioureas and acylguanidines from N-acyl cyanamides. Photoactivated reduction of aromatic disulfides in the presence of Huenig's base results in hydrothiolation of the cyanamide moiety, followed by spontaneous 1,3-migration of the acyl group. Onward reaction of the isothioureas obtained with amines led to the corresponding N-acylguanidines, where the acyl group is attached to the nitrogen atom formerly at the cyano-end of the starting material.