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116223-46-2

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116223-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116223-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,2 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116223-46:
(8*1)+(7*1)+(6*6)+(5*2)+(4*2)+(3*3)+(2*4)+(1*6)=92
92 % 10 = 2
So 116223-46-2 is a valid CAS Registry Number.

116223-46-2Downstream Products

116223-46-2Relevant articles and documents

Hydrogen bonded liquid crystal from nitrophenols and alkoxystilbazoles

Price, Daniel J.,Willis, Kimberly,Richardson, Tim,Ungar, Goran,Bruce, Duncan W.

, p. 883 - 892 (1997)

Tree series hydrogen bonded adducts have been formed between 4-alkoxy-4'-stilbazoles and the nitrophenols 4-nitrophenol, 3-nitrophenol and 2,4-dinitrophenol.Each series is mesomorphic displaying both nematic and smectic.A phases, in sharp contrast to the

Novel Ion Containing Liquid Crystals and Liquid Crystalline Main Chain Polymers Based on Trans-1,2-Bis(4-Pyridyl Ethylene) Mesogen

Cheng, P.,Blumstein, A.,Subramanyam, S.

, p. 1 - 38 (2007/10/02)

Ion bearing liquid crystalline compounds based on trans-1,2-bis(4-pyridinium)ethylene were synthesized and studied.These compounds included low molecular mass analogues, twin model compounds and main chain ionomers.Most of these exhibited liquid crystallinity of the smectic type.As a general rule the introduction of charges into the mesogenic moiety increased the stability (transition temperature) of the mesophase.Large supercooling effects, broad mesophase intervals and tendency to polymorphism are common features of these ionic mesogenic compounds.In the case of twin model compounds a variety of smectic phases were observed.The nature of these was dependent on the nature of the counterion and the thermal history of the compound.Tosylate or p.toluene sulfonate counterions promoted a higher degree of order in smectic mesophases as well as higher transition tempertures compared to methylsulfonate counterions.A pronounced odd-even effect of the isotropisation temperature of the twin compounds was observed.Compounds with even numbered methylene spacers display higher transition temperatures than those with an odd spacer.Only polymers with methylsulfonate and toluenesulfonate counterions were found to exhibit both, thermotropic and lyotropic mesophases.Thermotropic mesophases were characterized as smectic mesophases of lower order (SA).The nature of lyotropic mesophases were not determined.High transition temperatures and concommitant oxydative crosslinking made the study of polymers with halogen counterions difficult.Polymers with halogen and perchlorate counterions were found fo be poorly soluble in water precluding the formation of lyotropic mesophases.The introduction of a few siloxane bonds into the flexible spacer joining the charged mesogen moieties has a dramatic effect on lowering the transition temparatures and making possible the study of mesophases up to their isotropisation temperature.Preliminary characterization of polymers with siloxane containing spacer and methylsulfonate/tosylate counterions suggest a smectic mesophase of lower order. - Keywords: Ion containing liquid crystals, liquid crystal ionomers

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