61744-37-4

Basic information

• Product Name: N-(9H-xanthen-9-ylidene)aniline
• Synonyms: N-(9H-xanthen-9-ylidene)aniline
• CAS NO: 61744-37-4
• Molecular Weight: 271.318
• Mol File: 61744-37-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-(9H-xanthen-9-ylidene)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(9H-xanthen-9-ylidene)aniline(61744-37-4)
• EPA Substance Registry System: N-(9H-xanthen-9-ylidene)aniline(61744-37-4)

Safety Data

• Hazardous Substances Data: 61744-37-4(Hazardous Substances Data)

Upstream product

• 90-47-1 xanth-9-one 
• 62-53-3 aniline 
• 492-21-7 9H-xanthene-9-thione 
• 622-37-7 Phenyl azide 
• 20735-05-1 9,9-Dichloroxanthene 
• 4960-31-0 Tris(methylphenylamino)methan 
• 61744-33-0 9-azido-9-phenyl-xanthene 
• 150458-04-1 1-(9H-xanthen-9-yl)-1H-benzo[d][1,2,3]triazole 
• 596-38-3 9-phenyl-9H-xanthen-9-ol 
• 108-95-2 phenol 
• 19434-34-5 2-(phenoxy)benzaldehyde 
• 27090-15-9 9-(9'H-fluoren-9'-ylidene)-9H-xanthene 
• 1807-62-1 2-(9-xanthylidene)indane-1,3-dione 
• 91-17-8 decalin 

Downstream Products

• 492-21-7 9H-xanthene-9-thione 
• 33564-61-3 phenyl-xanthen-9-yl-amine 
• 92-83-1 xanthene 
• 90-47-1 xanth-9-one 
• 62-53-3 aniline 
• 33564-60-2 N,N'-diphenyl-N-xanthen-9-yl-urea 

Relevant articles and documents

Polycyclic fused phenanthridines: An alternative approach from benzotriazoles

We describe an alternative approach to polycyclic phenanthridines (7) and some of their analogues using conditions much milder than those previously reported. The procedure includes the generation of a benzotriazole stabilized carbanion, oxidation of the resulting anion to a radical, and elimination of nitrogen followed by ring closure to produce phenanthridines.

The thermal and photolytic decomposition of 9-aryl-9-xanthenyl azides to 11-aryldibenzo[b,f][1,4] oxazepines

In contrast to the different ratios of products obtained in the thermal decomposition of some 9-aryl-9-xanthenyl azides, it was found that photolysis afforded the same product ratio. The mechanism of these reactions is discussed in terms of intermediates as well as conformational and electronic effects in the transition states.

C = C Double Bonds with Extreme Reactivity, III. Reactions of 9-(9-Fluorenylidene)xanthene

According to equations (1) to (4), 9-(9-fluorenylidene)xanthene (2) reacts with sulfur, malonodinitrile, aniline, or thiophenol to give the compounds 3, 5, 7-11, and diphenyl disulfide.