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2-p-butoxybenzylideneamino-9,10-dihydrophenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82344-16-9

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82344-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82344-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82344-16:
(7*8)+(6*2)+(5*3)+(4*4)+(3*4)+(2*1)+(1*6)=119
119 % 10 = 9
So 82344-16-9 is a valid CAS Registry Number.

82344-16-9Downstream Products

82344-16-9Relevant academic research and scientific papers

Properties of the Liquid Crystals formed by Certain 2-p-Alkoxybenzylideneamino-9,10-dihydrophenanthrenes

Byron, David J.,Harwood, David J.,Wilson, Robert C.

, p. 197 - 200 (2007/10/02)

The liquid crystal transition temperatures of 11 2-p-alkoxybenzylideneamino-9,10-dihydrophenanthrenes are reported and discussed.Graphical presentation shows a fall to a minimum followed by a rise to a maximum for the N-I transition temperatures of the early homologues and lack of convergence of the rising SA-N and the falling N-I transition temperature curves for the higher homologues, i.e. there is persistence of nematic phases to a late stage in the homologous series.This behaviour is consistent with very low lateral cohesive forces operating throughout the homologous series.

The 9,10-Dihydrophenanthrene Structure as a Source of Liquid Crystals: Mesogenic Behaviour and Spectroscopic Properties of 2-Benzylideneamino-9,10-dihydrophenanthrenes

Behnam, Basil A.,Hall, D. Muriel

, p. 465 - 472 (2007/10/02)

13 Azomethines have been prepared from 2-amino-9,10-dihydrophenanthrene by reaction with aromatic aldehydes.Those with p-alkoxy, p-cyano or p-phenyl substituents in the aldehydic ring have a nematic mesophase.U.v. spectra, 1H and 13C n.m.r. spectra, and mass spectra of the series are discussed.Mass spectra show that ortho-substituents in the aldehydic ring substantially modify the fragmentation pattern.

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