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Benzenemethanol, 4-(heptadecafluorooctyl)-a-propyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

665026-64-2

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665026-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 665026-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,5,0,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 665026-64:
(8*6)+(7*6)+(6*5)+(5*0)+(4*2)+(3*6)+(2*6)+(1*4)=162
162 % 10 = 2
So 665026-64-2 is a valid CAS Registry Number.

665026-64-2Relevant articles and documents

Synthesis of phosphate-type fluorocarbon-hydrocarbon hybrid surfactants and their adsorption onto calcium hydroxyapatite

Miyazawa, Haruhiko,Yokokura, Hiroyuki,Ohkubo, Yuki,Kondo, Yukishige,Yoshino, Norio

, p. 1485 - 1490 (2007/10/03)

Five novel phosphate-type hybrid surfactants, Cm F2m+1C6H4CH[OPO2 (OC6H5)Na]CnH2n+1 (FmPHnPPhNa: m = 4, 6, 8; n = 3, 5), have been synthesized. When compared with sulfate-type hybrid surfactants, CmF2m+1C6H4 CH(OSO3Na)CnH2n+1 (C6H4 = p-phenylene), the new hybrid surfactants were found to have comparable abilities to lower the surface tension of water. The critical micelle concentrations of F m PH n PPhNa followed Klevens' rule and their occupied areas per molecule increased with increasing m and n. Calcium hydroxyapatite (CaHAp) pellets modified with FmPH3PPhNa gave high hydro and lipophobic surfaces. The hybrid surfactants are expected to be useful as new dental reagents for oral hygiene.

Synthesis and solution properties of sulfate-type hybrid surfactants with a benzene ring

Miyazawa, Haruhiko,Igawa, Kanako,Kondo, Yukishige,Yoshino, Norio

, p. 189 - 196 (2007/10/03)

Nine novel sulfate-type hybrid surfactants, Cm F2m+1C6H4CH(OSO3Na) CnH2n+1 (FmPHnOS: m=4, 6, 8; n=3, 5, 7; C6H4: p-phenylene), with a benzene ring in their molecules were synthesized. Alkanoyl chlorides were allowed to react with iodobenzene in the presence of aluminum chloride to give the corresponding aromatic ketones. The reaction of the ketones with perfluoroalkyl iodides yielded 1-[4-(perfluoroalkyl)phenyl]-1-alkanones as intermediates. The intermediates were allowed to react with methanol in tetrahydrofuran in the presence of sodium borohydride to yield 1-[4-(perfluoroalkyl)phenyl]-1-alkanols. The desired hybrid surfactants were obtained by the reaction of 1-[4-(perfluoroalkyl)phenyl-1-alkanols with sulfur trioxide/pyridine complex in pyridine and by the subsequent neutralization of the products with sodium hydroxide solution. When compared with the conventional hybrid surfactants, Cm F2m+1C6H4COCH(SO3Na) CnH2n+1 (FmHnS: m=4, 6; n=2, 4, 6; C6H4: p-phenylene), the new hybrid surfactants thus synthesized were found to have a comparable ability to lower the surface tension of water and a high hydrophilicity. The cmc of FmPH n OS obeyed Kleven's rule and their occupied areas per molecule increased with increasing m and n with the values between 0.66 and 1.05 nm2. The aggregation number for FmPHnOS micelles ranged from 6 to 45 and the hydrodynamic radius of the micelles was in the range of 1.4-3.1 nm.

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