675198-83-1

Basic information

• Product Name: 2,2'-(4-METHOXYPHENYLAZANEDIYL)BIS(1-PHENYLETHANONE)
• Synonyms: 2,2'-(4-METHOXYPHENYLAZANEDIYL)BIS(1-PHENYLETHANONE)
• CAS NO: 675198-83-1
• Molecular Formula: C₂₃H₂₁NO₃
• Molecular Weight: 359.42
• Mol File: 675198-83-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2'-(4-METHOXYPHENYLAZANEDIYL)BIS(1-PHENYLETHANONE)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-(4-METHOXYPHENYLAZANEDIYL)BIS(1-PHENYLETHANONE)(675198-83-1)
• EPA Substance Registry System: 2,2'-(4-METHOXYPHENYLAZANEDIYL)BIS(1-PHENYLETHANONE)(675198-83-1)

Safety Data

• Hazardous Substances Data: 675198-83-1(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 5883-82-9 2-((4-methoxyphenyl)amino)-1-phenylethanone 
• 104-94-9 4-methoxy-aniline 
• 70-11-1 α-bromoacetophenone 
• 98-86-2 acetophenone 

Downstream Products

• 859157-95-2 1-(4-methoxy-phenyl)-3,4-diphenyl-2,5-dihydro-1H-pyrrole 
• 112686-80-3 1-(4-methoxyphenyl)-3,4-diphenyl-1H-pyrrole 

Relevant articles and documents

Synthesis of oxathiane and morpholine from acyclic precursors: A modified Mitsunobu reaction

Synthesis of a set of isomeric 2,4,6-triarylmorpholines and 2,6-diaryloxathianes from the corresponding 1,5-diols has been described. The method provides an efficient route to six-membered heterocycles from acyclic diols and is found to be better than Mitsunobu procedure in yield and waste management. In a related study, the ring contraction of pyranone to two isomeric cyclopentenone derivatives through Nazarov reaction has been noticed.

A new approach to the preparation of 1,3,4-triarylpyrroles

A class of 1,3,4-triaryl-2,5-dihydropyrroles were synthesized using the McMurry coupling reaction as the key step. The non-catalytic photoconversion of 1,3,4-triaryl-2,5-dihydropyrroles furnished 1,3,4-triarylpyrroles in good yields (63-89%). It was found

Study on photochromism of diarylethenes with a 2,5-dihydropyrrole bridging unit: A convenient preparation of 3,4-diarylpyrroles from 3,4-diaryl-2,5- dihydropyrroles

Symmetric and nonsymmetric diarylethenes with a 2,5-dihydropyrrole bridging unit have been prepared, and the photochromic properties are investigated. Both symmetric and nonsymmetric diarylethenes with 2,5-dihydropyrrole bridging units undergo reversible ring-opening and ring-closing photoisomerization reactions in nonpolar solvents with UV/vis light, and some of them exhibit good fatigue resistance and no marked degradation detected after 10 cycles via an on/off switch. In polar solvents, however, photochromic diarylethenes with 2,5-dihydropyrrole bridging units produce 3,4-diarylpyrrole derivatives instead of the ring-closing isomer of diarylethenes with UV light irradiation. A class of N-substituted 3,4-diphenylethenes with 2,5-dihydropyrrole bridging units were prepared and used as templates to investigate the conversion reactions. The mechanism of photoconversion of 3,4-diaryl-2,5-dihydropyrroles to 3,4-diarylpyrroles was explored as well.