122744-71-2

Basic information

• Product Name: 1,2,4,5-Trioxazine, 6-heptyldihydro-3-phenyl-5-(phenylmethyl)-
• CAS NO: 122744-71-2
• Molecular Formula: C22H29NO3
• Molecular Weight: 355.477
• Mol File: 122744-71-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,2,4,5-Trioxazine, 6-heptyldihydro-3-phenyl-5-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4,5-Trioxazine, 6-heptyldihydro-3-phenyl-5-(phenylmethyl)-(122744-71-2)
• EPA Substance Registry System: 1,2,4,5-Trioxazine, 6-heptyldihydro-3-phenyl-5-(phenylmethyl)-(122744-71-2)

Safety Data

• Hazardous Substances Data: 122744-71-2(Hazardous Substances Data)

Upstream product

• 4747-15-3 1-(2-methoxyvinyl)benzene 
• 72552-76-2 α-Heptyl-N-benzylnitrone 
• 4110-75-2 (E)-(2-methoxyvinyl)benzene 

Downstream Products

• 139633-09-3 N-Benzyl-N-octylhydroxylamine 
• 100-51-6 benzyl alcohol 
• 124-13-0 Octanal 
• 72552-76-2 α-Heptyl-N-benzylnitrone 
• 65-85-0 benzoic acid 
• 932-90-1 Benzaldoxime 
• 100-52-7 benzaldehyde 
• 16204-37-8 3,6-diphenyl-1,2,4,5-tetraoxane 
• 622-30-0 N-benzyl hydroxylalmine 
• 3481-15-0 benzyl alcohol-d1 
• 932-90-1 syn-benzaldehyde oxime 
• 91-01-0 1,1-Diphenylmethanol 
• 139633-07-1 N-Benzyl-N-(1-phenyloctyl)hydroxylamine 
• 98-85-1 1-Phenylethanol 

Relevant articles and documents

Synthesis and X-ray Analysis of Dihydro-1,2,4,5-trioxazine. Evidence of a Steowise Mechanism for the Cycloaddition of Carbonyl Oxides with Nitrones

Carbonyl oxides, derived by ozonolysis of vinyl ethers, readily undergo cycloaddition reactions with nitrones affording dihydro-1,2,4,5-trioxazines in fair to excellent yield.The structures of dihydro-3,5,6-triphenyl-1,2,4,5-trioxazine (5f) and dihydro-3-cyclohexyl-5-methyl-6,6-diphenyl-1,2,4,5-trioxazine (5t) were unambiguously determined by X-ray analysis.Ozonolysis of 1-cyclohexyl-2-methoxyethene in the presence of either (E)- or (Z)-α-(4-methylphenyl)-α-phenyl-N-methylnitrone gave a 1:1 mixture of two stereoisomeric cycloadducts.This result, in conjunction with the structure of the relevant 5t, suggests that the cycloaddition proceeds by a stepwise mechanism.