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2-hydroxy-4'-butyl-3-naphthanilide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95572-51-3

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95572-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95572-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,7 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95572-51:
(7*9)+(6*5)+(5*5)+(4*7)+(3*2)+(2*5)+(1*1)=163
163 % 10 = 3
So 95572-51-3 is a valid CAS Registry Number.

95572-51-3Relevant academic research and scientific papers

Black azo-metal complex, photosensitive resin compositions containing thereof and cured films prepared using the composition

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Paragraph 0166-0170, (2018/07/28)

The present invention relates to a black azo-metal complex, a photosensitive resin composition containing the same and a color filter prepared by using the same, wherein the black azo-metal complex of the present invention has excellent thermal stability, chemical resistance and solubility, so that the photosensitive resin composition and the color filter using the same have excellent optical properties such as color retention rate, optical density and surface resistance.COPYRIGHT KIPO 2018

TAUTOMERISM IN THE DERIVATIVES OF 1-PHENYLAZO-2-HYDROXY-3-NAPHTHANILIDE

Zaitsev, B. E.,Sycheva, E. D.,Sheban, G. V.,Lisitsyna, E. S.,Mikhailova, T. A.,et al.

, p. 1556 - 1564 (2007/10/02)

The spectroscopic criteria for the presence of the azo and quinone hydrazone tautomers were obtained by analysis of the data from electronic spectroscopy and quantum-chemical calculation of the derivatives of 1-phenylazo-2-hydroxy-3-naphthanilide and the fixed forms of the tautomers; the ratio of the azo and quinone hydrazone tautomers depends on the polarity of the solvent; in the transition from chloroform to dimethylformamide the content of the azo form changes from 14.6 to 30.1 percent. "Anomalous" changes in the spectra of 1-arylazo-2-hydroxy-3-naphthanilides compared with the spectra of 1-phenylazo-2-naphthol are brought about by the overlap of the long-wave bands of the azo and quinone hydrazone tautomers with the band for charge transfer from the anilide group to the azo or quinone hydrazone system.

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