10183-83-2

Basic information

• Product Name: N-(9H-fluoren-9-ylidene)-4-methylaniline
• Synonyms: N-(9H-fluoren-9-ylidene)-4-methylaniline
• CAS NO: 10183-83-2
• Molecular Weight: 269.346
• Mol File: 10183-83-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(9H-fluoren-9-ylidene)-4-methylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(9H-fluoren-9-ylidene)-4-methylaniline(10183-83-2)
• EPA Substance Registry System: N-(9H-fluoren-9-ylidene)-4-methylaniline(10183-83-2)

Safety Data

• Hazardous Substances Data: 10183-83-2(Hazardous Substances Data)

Upstream product

• 486-25-9 9-fluorenone 
• 15795-42-3 N-sulfinyl-4-methylaniline 
• 36804-63-4 1-bromo-9H-fluoren-9-one 
• 36804-56-5 1-chloro-9H-fluoren-9-one 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 106-49-0 p-toluidine 

Downstream Products

• 486-25-9 9-fluorenone 
• 106-49-0 p-toluidine 
• 1344727-66-7 1-(4-methylphenyl)-dispiro[azetidine((2,9'-fluorene)(3,9'-xanthene))]-4-one 
• 1344727-60-1 3-phenoxy-1-p-tolylspiro[azetidine-2,9'-fluoren]-4-one 
• 62614-21-5 9-N-(p-Methylphenyl)aminofluorenphosphonsaeure-9 
• 66783-76-4 4'-tert-butyl-5'-oxo-3'-p-tolyl-spiro[fluorene-9,2'-oxazolidine]-4'-carboxylic acid ethyl ester 
• 66783-78-6 4'-tert-butyl-5'-oxo-3'-p-tolyl-spiro[fluorene-9,2'-oxazolidine]-4'-carbonitrile 
• 62614-13-5 (9-p-Tolylamino-9H-fluoren-9-yl)-phosphonic acid diethyl ester 
• 119437-50-2 N-(4-methylphenyl)-9-butyl-9-aminofluorene 
• 119437-49-9 N-butyl-N-(4-methylphenyl)-9-aminofluorene 
• 66783-82-2 N-(9H-fluorene-9-ylidine)-4-methylaniline oxide 

Relevant articles and documents

Nitrogen-doped graphitic carbon synthesized by laser annealing of sumanenemonoone imine as a bowl-shaped π-conjugated molecule

Time for tuning: Nitrogen-doped graphitic carbon was synthesized from a bowl-shaped π-conjugated compound bearing an imine moiety; this bowl-shaped compound underwent carbonization through laser annealing while almost retaining the nitrogen/carbon ratio.

Synthesis of mono-, bis-spiro- and dispiro-β-lactams and evaluation of their antimalarial activities

Some new mono-, bis-spiro- and dispiro-β-lactams have been synthesized from imines derived from 9H-fluoren-9-one and a ketene derived from 9H-xanthene-9-carboxylic acid or phenoxyacetic acid by a [2+2] cycloaddition reaction in good to excellent yields va

The Replacement of Electronegative Substituents by an Electron-transfer Mechanism. The Factors Governing the Reaction of Carbonyl and Imino Compounds with Organomagnesium Reagents

For the purpose of studying the electron-transfer initiated replacement of ortho-methoxy and ortho-halogeno substituents of diaryl ketone anils by the aryl group of ArMgBr, eight anils were prepared.The expected o-methoxy replacement by the phenyl group o