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57242-02-1

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57242-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57242-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,4 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57242-02:
(7*5)+(6*7)+(5*2)+(4*4)+(3*2)+(2*0)+(1*2)=111
111 % 10 = 1
So 57242-02-1 is a valid CAS Registry Number.

57242-02-1Downstream Products

57242-02-1Relevant articles and documents

Aromatic Esters, Carbinols, and Derivatives Thereof with Perfluorohexyl Residues as Alternatives to Perfluoroalkanecarboxylic and -sulfonic Acids

Alpers, Torben,Muesmann, Thomas W. T.,Temme, Oliver,Christoffers, Jens

, p. 609 - 617 (2017/02/05)

Four perfluorohexyl carbinols have been prepared from the corresponding Grignard reagent and benzaldehyde, terephthalaldehyde, isophthalaldehyde, and trimesaldehyde. The corresponding secondary alcohols were then transformed by alkylation and acylation reactions to form a total of 14 ethers (methyl, ethyl, propyl, and n-hexyl ethers) and esters (acetyl and 2-ethylhexanoyl), respectively. Furthermore, 11 perfluoroalkyl carboxylates were prepared from aromatic, heteroaromatic, and aliphatic mono-, di-, tri-, and tetracarboxylic acids and tridecafluorooctanol. The wettability of all 29 materials was investigated by the water contact angle measurements of thin films on glass surfaces. In up to six cases, contact angles greater than 130° were observed, which indicates that the products might be suitable candidates for the impregnation of surfaces. With their relatively short perfluoroalkyl side-chains and therefore low bioaccumulativity, the target compounds might be beneficial alternatives to established products.

Perfluoroalkyl and -aryl Zinc Ate Complexes: Generation, Reactivity, and Synthetic Application

Wang, Xuan,Hirano, Keiichi,Kurauchi, Daisuke,Kato, Hisano,Toriumi, Naoyuki,Takita, Ryo,Uchiyama, Masanobu

supporting information, p. 10993 - 10996 (2015/11/10)

A combination of dimethylzinc, perfluoroalkyl iodide, and LiCl afforded a new type of perfluoroalkyl (RF) zinc ate complex. These complexes show much greater thermal stability than conventional perfluorinated metal species, such as RF-lithium species and Grignard reagents, and they can be used at room temperature or higher. The results of DFT calculations on the origin of the enhanced stability are reported and the synthetic utility of RF-zincate complexes is demonstrated. The magnificent ate: A combination of dimethylzinc, perfluoroalkyl iodide, and LiCl afforded a new type of perfluoroalkyl (RF) zinc ate complex. These complexes show greater thermal stability than conventional perfluorinated metal species and they can be used at room temperature or higher. The results of DFT calculations on the origin of the enhanced stability are reported and the synthetic utility of RF-zincate complexes is demonstrated.

Paradigm shift from alkaline (earth) metals to early transition metals in fluoroorganometal chemistry: Perfluoroalkyl titanocene(III) reagents prepared via not titanocene(II) but titanocene(III) species

Fujiu, Motohiro,Hashimoto, Ryota,Nakamura, Yuzo,Aikawa, Kohsuke,Ito, Shigekazu,Mikami, Koichi

supporting information, p. 2382 - 2386 (2014/03/21)

Perfluoroalkyl (RF) titanocene reagents [Cp2Ti IIIRF] synthesized via [Cp2TiIIICl] rather than [Cp2TiII] show new types of perfluoroalkylation reactions. The [Cp2TiIIIRF] reagents exhibit a wide variety of reactivity with carbonyl compounds including esters and nitriles, and selectivities far higher than those reported for conventional RFLi and RFMgX reagents. Copyright

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