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Phenol, 4-[(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

683795-22-4

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683795-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 683795-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,3,7,9 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 683795-22:
(8*6)+(7*8)+(6*3)+(5*7)+(4*9)+(3*5)+(2*2)+(1*2)=214
214 % 10 = 4
So 683795-22-4 is a valid CAS Registry Number.

683795-22-4Relevant academic research and scientific papers

Liquid crystal and gel properties of fluorine containing compound

Jang, Jun Yeol,Park, Young Wook

, p. 22 - 31 (2017)

A series of (2-perfluorohexyl)-ethoxy phenyl 4-alkyl benzoate (F6H2OPCnB) was synthesized, and liquid crystals (LCs) and gelation properties were studied. The isotropic temperature (TI) showed good even-odd effect. The compound with an odd number of carbon atoms in the alkyl chain possessed a higher temperature. Tm showed weak even-odd effect. However the transition showed an opposite alternation. The mesomorphic structure of those compounds was smectic A or E. The structure of the compound was bimolecular kinked structure. F6H2OPCnB gel (10?wt.% in propylene carbonate) was studied. Tgel of F6H2OPC2B showed the highest value due to its high Tm (crystal melting temperature). Tgel (gel melting temperature) was strongly dependent on Tm. F6H2OPC6B gel showed the highest value in heat of fusion. The gel's heat of fusion was a good parameter of the gel stability.

Effects of chemical variations on the mesophase behavior of new fluorinated poly(vinylcyclopropane)s

Ragnoli, Marina,Pucci, Elena,Bertolucci, Massimo,Gallot, Bernard,Galli, Giancarlo

, p. 283 - 292 (2007/10/03)

Several new structures of fluorinated polymers poly(1)-poly(9) were prepared by free radical ring opening polymerization of vinylcyclopropane monomers 1-9 containing different fluorinated side groups of the type -(CH2)n(CF2) pF. While in poly(1)-poly(3) p varied from 6 to 10 for a fixed n=2, in poly(4)-poly(6) n increased from 3 to 5 at the given p=8. In poly(7) and poly(8) a phenyl ring was incorporated to elongate the mesogenic side group (n=2; p=6 and 8, respectively), that was further separated from the polymer backbone by a methylene spacer (m=11) in poly(9). Therefore, the effects of various chemical variations of the polymer structure on the mesophase behavior could be assessed. The polymers were in fact co-polymers comprising both 1,5-linear and cyclobutane-ring isomer units. In any case they formed smectic mesophase(s) owing to the special character of the perfluorinated chains. The order and the isotropization temperature (Ti) of the mesophase were enhanced by increasing p, but Ti lowered with increasing n. Extension of the side group by insertion of a phenyl ring improved Ti. Wide angle X-ray diffraction studies clarified the nature of the different smectic phases, the occurrence of which was discussed in terms of the ability of the fluorinated side groups to pack antiparallel in either a partly or fully interdigitated structure. Co-polymers of 3 with a non-mesogenic, not fluorinated co-monomer 10 were also prepared with different chemical compositions. Co-polymerization was found to be another effective means of modifying the mesophase behavior of the poly(vinylcyclopropane)s.

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