55361-37-0

Basic information

• Product Name: 3'-(4-nitro-phenyl)-2-phenyl-3-piperidin-1-yl-spiro[indene-1,5'-[1,4,2]oxathiazole]
• Synonyms: 3'-(4-nitro-phenyl)-2-phenyl-3-piperidin-1-yl-spiro[indene-1,5'-[1,4,2]oxathiazole]
• CAS NO: 55361-37-0
• Molecular Weight: 469.564
• Mol File: 55361-37-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3'-(4-nitro-phenyl)-2-phenyl-3-piperidin-1-yl-spiro[indene-1,5'-[1,4,2]oxathiazole](CAS DataBase Reference)
• NIST Chemistry Reference: 3'-(4-nitro-phenyl)-2-phenyl-3-piperidin-1-yl-spiro[indene-1,5'-[1,4,2]oxathiazole](55361-37-0)
• EPA Substance Registry System: 3'-(4-nitro-phenyl)-2-phenyl-3-piperidin-1-yl-spiro[indene-1,5'-[1,4,2]oxathiazole](55361-37-0)

Safety Data

• Hazardous Substances Data: 55361-37-0(Hazardous Substances Data)

Upstream product

• 2574-03-0 p-nitrobenzonitrile oxide 
• 53215-50-2 3-piperidino-2-phenyl-1-indenethione 
• 1011-84-3 4-nitrobenzohydroximoyl chloride 

Relevant articles and documents

α,β-UNSATURATED THIO COMPOUNDS. XX. -CYCLOADDITION OF 3-AMINO-2-ARYL-1-INDENETHIONES TO NITRILIUM BETAINES AND PHENYL AZIDE

N,N-Disubstituted 3-amino-2-aryl-1-indenethiones react with the N-oxides of aromatic nitriles or with benzonitrile phenylimine to form 5-spiroindene-substituted 1,4,2-oxathiazoles and 2-spiroindene-substituted 1,3,4-thiadiazolines.With phenyl azide only the transformation of the thiocarbonyl group into a phenylimine group occurs.In the reaction of N-unsubstituted aminoindenethione with benzonitrile N-oxide N,N-diacylation and the parallel transformation of the thione function into ketone function are observed.The reaction of 3-phenylamino-1-indenethione in the iminoenethiol form with benzonitrile N-oxide leads to the product from S-acylation and cycloaddition at the C=N bond with the formation of a 1,4,2-oxadiazoline ring.