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4-nitro-N-4-methoxyphenylnaphthalic-1,8-imide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42340-36-3

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42340-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42340-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42340-36:
(7*4)+(6*2)+(5*3)+(4*4)+(3*0)+(2*3)+(1*6)=83
83 % 10 = 3
So 42340-36-3 is a valid CAS Registry Number.

42340-36-3Relevant academic research and scientific papers

Synthesis and spectral properties of 4-amino-and 4-acetylamino-N- arylnaphthalimides containing electron-donating groups in the N-aryl substituent

Panchenko,Fedorova,Perevalov,Jonusauskas,Fedorov

experimental part, p. 1233 - 1240 (2010/10/04)

A method for the synthesis of N-aryl-substituted 4-amino-and 4-acetylaminonaphthalimide derivatives with mono-and dialkoxy groups or a 15-crown-5 moiety in the N-aryl substituent is described. The introduction of electron-donating alkoxy groups into the benzene ring of the N-aryl fragment results in fluorescence quenching of the naphthalimide chromophore, which is most pronounced in the spectra of N-acetyl derivatives. The photophysical properties of the synthesized 4-amino-and 4-acetylaminonaphthalimides depend on the solvent polarity and its specific solvating ability due to H-bonding. The crown-containing compounds are promising fluorescent chemosensors for metal cations. ; 2009 Springer Science+Business Media, Inc.

Fluorescent compounds from reactions of nitrobenzimidazylbenzisoquinolines from 4-nitronaphthalic anhydride with alkylamines

Alexiou,Tyman

, p. 56 - 58 (2007/10/03)

The nitro group in the isomeric condensation products of 4-nitronaphthalic-1,8-anhydride with 1,2-diaminobenzene namely 3-nitro and 4-nitro-7H-benzimidazo[2,1-a]benz[de]isoquinolin-7-one is displaced by reaction with 1-octylamine, to give in the case of the 4-nitro compound the highly fluorescent 4-octylamino derivative. The condensation product from 4,5-dinitronaphthalic-1,8-anhydride and 1,2-diaminobenzene afforded, by nitro group displacement with either 1-butylamine or 1-octylamine, complex mixtures without exhibiting significant fluorescence.

Synthesis and properties of fluorescent 1,8-naphthalimide dyes for application in liquid crystal displays

Grabchev, Ivo,Moneva, Ivanka,Bojinov, Vladimir,Guittonneau, Sylvie

, p. 1291 - 1296 (2007/10/03)

A series of highly fluorescent 1,8-naphthalimide derivatives having an N-allylamino group at position 4 of the aromatic structure have been synthesised, and some of their properties for application in liquid crystal displays have been determined. The opti

SYNTHESIS OF 4-ALKYLAMINONAPHTHALIMIDES AND STUDY OF THEIR LUMINESCENT AND ORIENTATIONAL CHARACTERISTICS IN THE LIQUID-CRYSTALLINE MATRIX

Lugovskii, A. P.,Rachkevich, V. S.,Erdman, M. V.

, p. 560 - 563 (2007/10/02)

4-Alkylaminonaphthalimides were obtained by nucleophilic substitution of the nitro group in 4-nitro-N-arylnaphthylimides.The luminescence-spectral characteristics of their solutions in toluene, alcohol, and a liquid-crystalline matrix were studied.The deg

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