1439383-38-6

Basic information

• Product Name: 1,3',5-trimethyl-2'-phenylspiro[1,5-diazinane-3,1'-indene]-2,4,6-trione
• Synonyms: 1,3',5-trimethyl-2'-phenylspiro[1,5-diazinane-3,1'-indene]-2,4,6-trione
• CAS NO: 1439383-38-6
• Molecular Weight: 346.386
• Mol File: 1439383-38-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3',5-trimethyl-2'-phenylspiro[1,5-diazinane-3,1'-indene]-2,4,6-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3',5-trimethyl-2'-phenylspiro[1,5-diazinane-3,1'-indene]-2,4,6-trione(1439383-38-6)
• EPA Substance Registry System: 1,3',5-trimethyl-2'-phenylspiro[1,5-diazinane-3,1'-indene]-2,4,6-trione(1439383-38-6)

Safety Data

• Hazardous Substances Data: 1439383-38-6(Hazardous Substances Data)

Upstream product

• 2613-89-0 phenylmalonic acid 
• 673-32-5 1-Phenylprop-1-yne 
• 7391-66-4 1,3-dimethyl-5-phenyl-pyrimidine-2,4,6(1H,3H,5H)-trione 

Relevant articles and documents

Functionalization of Csp3-H and Csp 2-H bonds: Synthesis of spiroindenes by enolate-directed ruthenium-catalyzed oxidative annulation of alkynes with 2-aryl-1,3-dicarbonyl compounds

Ru(de) awakening: The synthesis of carbocycles by the ruthenium-catalyzed oxidative annulation of alkynes with 2-aryl cyclic 1,3-dicarbonyl substrates is described. Proceeding by the functionalization of C sp 3-H and C sp 2-H bonds, and the formation of an all-carbon quaternary center, the reaction provides a diverse range of spiroindenes in good yields with high levels of regioselectivity. Copyright