79628-37-8

Basic information

• Product Name: 1-<2,6-dinitro-4-(1,2,3,4-tetrahydro-4-phenyl-1-naphthyl)-phenyl>-2,2-diphenylhydrazine
• Synonyms: 1-<2,6-dinitro-4-(1,2,3,4-tetrahydro-4-phenyl-1-naphthyl)-phenyl>-2,2-diphenylhydrazine
• CAS NO: 79628-37-8
• Molecular Weight: 556.621
• Mol File: 79628-37-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-<2,6-dinitro-4-(1,2,3,4-tetrahydro-4-phenyl-1-naphthyl)-phenyl>-2,2-diphenylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-<2,6-dinitro-4-(1,2,3,4-tetrahydro-4-phenyl-1-naphthyl)-phenyl>-2,2-diphenylhydrazine(79628-37-8)
• EPA Substance Registry System: 1-<2,6-dinitro-4-(1,2,3,4-tetrahydro-4-phenyl-1-naphthyl)-phenyl>-2,2-diphenylhydrazine(79628-37-8)

Safety Data

• Hazardous Substances Data: 79628-37-8(Hazardous Substances Data)

Upstream product

• 147506-92-1 2,2-diphenyl-1-(2,4,6-trinitrophenyl)hydrazyl 
• 79628-38-9 bis(1,2,3,4-tetrahydro-4-phenyl-1,1-naphthyl)diazene 
• 19995-99-4 1,2,3,4-tetrahydro-4-(4-hydroxyphenyl)-1-phenylnaphthalene 
• 79628-46-9 1,2,3,4-tetrahydro-4-(4-methoxyphenyl)-1-phenylnaphthalene 
• 530-47-2 N,N-diphenylhydrazine hydrochloride 
• 100-42-5 styrene 

Relevant articles and documents

Products of reaction between styrene and some radicals with 2,2-diphenyl-1-picrylhydrazyl

Addition of 2,2-diphenyl-1-picrylhydrazyl DPPH to styrene at 75 deg C results in little change in the amounts of cis- and trans-1,2-diphenylcyclobutane and 1,2,3,4-tetrahydro-1-phenylnaphthalene, in a slightly smaller amount of 1-phenylnaphthalene, and in a considerable increase in the amount of 1,2-dihydro-1-phenylnaphthalene that are formed.Formation of the styrene trimer 1,2,3,4-tetrahydro-1-phenyl-4-(1-phenylethyl)naphthalene is eliminated completely.Products derived from DPPH are 1-(4-nitrophenyl)-1-phenyl-2-picrylhydrazine 9 and 1--2,2-diphenylhydrazine, 10.DPPH intercepts the thermally formed Diels-Alder dimer of styrene as soon as it is formed to give the 1,2,3,4-tetrahydro-4-phenyl-1-naphthyl radical.Thermolysis of bis(1,2,3,4-tetrahydro-4-phenyl-1-naphthyl)diazene in the presence of DPPH yields 20percent of 10, 10percent of 1--2-(4-nitrophenyl)-2-phenylhydrazine and 9 while thermolysis of 1,2-bis(1-phenylethyl)diazene in the presence of DPPH yields 9 and 44percent of 1--2,2-diphenylhydrazine showing that substituted benzyl radicals efficiently displace the 4-nitro group of DPPH.The nitro group is transferred to an unsubstituted phenyl group of DPPH.