5455-02-7

Basic information

• Product Name: N-(4-methoxyphenyl)fluoren-9-imine
• Synonyms: N-(4-methoxyphenyl)fluoren-9-imine
• CAS NO: 5455-02-7
• Molecular Formula: C₂₀H₁₅NO
• Molecular Weight: 0
• Mol File: 5455-02-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 450.7 °C at 760 mmHg
• Flash Point: 181.9 °C
• Appearance: /
• Density: 1.13 g/cm³
• Vapor Pressure: 6.87E-08mmHg at 25°C
• Refractive Index: 1.625
• CAS DataBase Reference: N-(4-methoxyphenyl)fluoren-9-imine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxyphenyl)fluoren-9-imine(5455-02-7)
• EPA Substance Registry System: N-(4-methoxyphenyl)fluoren-9-imine(5455-02-7)

Safety Data

• Hazardous Substances Data: 5455-02-7(Hazardous Substances Data)

Usage

General Description

N-(4-Methoxyphenyl)fluoren-9-imine, also known as 9-anilinofluorene or 4-methoxy-N-phenyl-9H-fluoren-9-imine, is a chemical compound that consists of a fluorene core with an aniline group substituted at the 9-position and a methoxy group attached to the phenyl ring. N-(4-Methoxyphenyl)fluoren-9-imine is commonly used in the synthesis of organic materials, such as dyes and pigments, as well as in the production of pharmaceuticals and agrochemicals. It is also used as a building block for the construction of heterocyclic compounds and as a reagent in various chemical reactions. N-(4-Methoxyphenyl)fluoren-9-imine has potential applications in the fields of material science and medicinal chemistry due to its unique structure and properties.

InChI:InChI=1/C20H15NO/c1-22-15-12-10-14(11-13-15)21-20-18-8-4-2-6-16(18)17-7-3-5-9-19(17)20/h2-13H,1H3

Upstream product

• 486-25-9 9-fluorenone 
• 104-94-9 4-methoxy-aniline 
• 13165-69-0 p-methoxy-N-sulfinylaniline 
• 1836-87-9 9-Benzylidene-9H-fluorene 
• 2101-87-3 p-methoxy-phenylazide 

Downstream Products

• 1344727-61-2 1-(4-methoxyphenyl)-3-phenoxyspiro[azetidine-2,9'-fluoren]-4-one 
• 1344727-67-8 1-(4-methoxyphenyl)-dispiro[azetidine((2,9'-fluorene)(3,9'-xanthene))]-4-one 
• 70765-98-9 4'-tert-butyl-3'-(4-methoxy-phenyl)-5'-oxo-spiro[fluorene-9,2'-oxazolidine]-4'-carbonitrile 
• 103210-42-0 N-fluoren-9-yl-N-(4-methoxy-phenyl)-N'-phenyl-urea 
• 102549-06-4 N-fluoren-9-yl-N-(4-methoxy-phenyl)-acetamide 
• 65161-96-8 9-Chloro-9-(N-p-methoxyphenylcarbamoyl)fluorene 
• 107973-09-1 5'-Methoxyspiro 
• 65161-88-8 3',3'-Dichloro-1'-(p-methoxyphenyl)spiro 
• 66783-83-3 N-(9H-fluorene-9-ylidine)-4-methoxyaniline oxide 
• 102078-78-4 N-(4-methoxyphenyl)-9H-fluoren-9-amine 

Relevant articles and documents

Rh(III)-catalyzed synthesis of 1-substituted isoquinolinium salts via a C-H bond activation reaction of ketimines with alkynes

An efficient synthesis of highly substituted isoquinolinium salts from ketimines and alkynes via a Rh(III)-catalyzed C-H bond activation and annulation reaction is described. The Royal Society of Chemistry.

Oxo/imido heterometathesis of N-sulfinylamines and carbonyl compounds catalyzed by silica-supported vanadium oxochloride

A series of silica-supported vanadium oxo complexes has been prepared via water-free grafting VOCl3 onto the silica surface. The obtained materials have been characterized with Raman, diffuse reflectance FTIR (DRIFT) and UV-vis, 51V

Reactions of Spiro

Methylenefluorene 3a adds regiospecifically to aryl azides 4 to give the corresponding spiro 5, which lead to the ring-enlargement products, 9-(arylamino)phenanthrenes (9), by pyrolysis and acid-induced reaction.Benzylidenefluorene 3b