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4-Chloro-N-(9H-fluoren-9-ylidene)aniline is an organic compound with the chemical formula C20H14ClN. It is a derivative of aniline, featuring a 9H-fluoren-9-ylidene group attached to the nitrogen atom and a chlorine atom at the 4-position of the aniline ring. 4-chloro-N-(9H-fluoren-9-ylidene)aniline is known for its potential applications in the synthesis of various dyes, pigments, and pharmaceuticals due to its unique chemical structure. The presence of the fluoren-9-ylidene group imparts specific electronic properties and reactivity, making it a valuable intermediate in organic synthesis. The compound is typically synthesized through a condensation reaction involving aniline and a fluorenone derivative, and its properties can be further explored for the development of new materials and compounds.

5455-00-5

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5455-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5455-00-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5455-00:
(6*5)+(5*4)+(4*5)+(3*5)+(2*0)+(1*0)=85
85 % 10 = 5
So 5455-00-5 is a valid CAS Registry Number.

5455-00-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-chlorophenyl)fluoren-9-imine

1.2 Other means of identification

Product number -
Other names N-(9H-fluoren-9-ylidene)-4-chlorobenzenamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5455-00-5 SDS

5455-00-5Relevant academic research and scientific papers

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

Jarrahpour, Aliasghar,Ebrahimi, Edris,De Clercq, Erik,Sinou, Véronique,Latour, Christine,Djouhri Bouktab, Lamia,Brunel, Jean Michel

experimental part, p. 8699 - 8704 (2011/12/02)

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

Intramolecular Addition of Aryl Radicals to Carbon-Nitrogen Double Bonds

Gioanola, Milena,Leardini, Rino,Nanni, Daniele,Pareschi, Patrizia,Zanardi, Giuseppe

, p. 2039 - 2054 (2007/10/02)

Cyclisation of radicals 6a,b is highly regioselective towards a 5-exo process; 6-endo ring closure is a minor route and their ratio depends on the substituents.No ring expansion of the five-membered radical intermediates 7a,b was observed.Radicals 27a,b give rise to 5-exo cyclisation regiospecifically.A competitive 1,5-hydrogen shift leading to imidoyl radicals was noticed.An analogous behaviour is also exhibited by vinyl radicals when allowed to add to carbon-nitrogen double bonds.

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