1005348-16-2

Basic information

• Product Name: N-(3,3-dimethylallyl)-N'-N-bis-Cbz-guanidine
• Synonyms: N-(3,3-dimethylallyl)-N'-N-bis-Cbz-guanidine
• CAS NO: 1005348-16-2
• Molecular Weight: 395.458
• Mol File: 1005348-16-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(3,3-dimethylallyl)-N'-N-bis-Cbz-guanidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,3-dimethylallyl)-N'-N-bis-Cbz-guanidine(1005348-16-2)
• EPA Substance Registry System: N-(3,3-dimethylallyl)-N'-N-bis-Cbz-guanidine(1005348-16-2)

Safety Data

• Hazardous Substances Data: 1005348-16-2(Hazardous Substances Data)

Upstream product

• 26728-58-5 (3-methyl-2-butenyl)amine hydrochloride 
• 25508-20-7 N,N'-dibenzyloxycarbonyl-(S)-methyl-isothiourea 
• 152120-55-3 N,N-bis(benzyloxycarbonyl)-1H-pyrazole-1-carboxamidine 

Downstream Products

• 1262675-48-8 benzyl 2-(((benzyloxy)carbonyl)imino)-4-(iodomethyl)-5,5-dimethylimidazolidine-1-carboxylate 
• 1262675-43-3 C₂₂H₂₄IN₃O₄ 

Relevant articles and documents

Halocyclization of Unsaturated Guanidines Mediated by Koser's Reagent and Lithium Halides

The synthesis of halogenated cyclic guanidines through iodine(III)-mediated umpolung of halide salts is described. Cyclic guanidines of various sizes can be obtained with generally excellent regioselectivities through either a chloro- or a bromocyclization, using Koser's reagent and the corresponding lithium salt.

Cyclisation reactions of bis-protected guanidines

The cyclisation of N-allyl- and N-homoallylguanidines using DMDO or I2/K2CO2 leading to novel heterocycles is reported.