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1,1,1,2,2,3,3-heptafluoro-4-phenylbutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81664-99-5

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81664-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81664-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81664-99:
(7*8)+(6*1)+(5*6)+(4*6)+(3*4)+(2*9)+(1*9)=155
155 % 10 = 5
So 81664-99-5 is a valid CAS Registry Number.

81664-99-5Downstream Products

81664-99-5Relevant academic research and scientific papers

Synthesis of functionalized long-chain perfluoroalkanes from methyl halodifluoroacetates: a process of difluorocarbene insertion into copper-carbon bonds

Su, De-Bao,Duan, Jian-Xing,Yu, An-Juan,Chen, Qing-Yun

, p. 11 - 14 (2007/10/02)

Treatment of XCF2CO2Me (X = Cl, Br) with organic halides in the presence of KF and catalytic amounts of CuI at 80-120 deg C for 3-8 h in DMF gave long-chain perfluoroalkylated compounds which are considered to be former by the insertions of CF2(..) into carbon-copper bonds.

The reactions of copper-dibromodifluoromethane-amide systems with alcohols

Clark, James H.,McClinton, Martin A.,Blade, Robert J.

, p. 257 - 267 (2007/10/02)

1,1,1-Trifluoro-2-arylethanes can be prepared by the trifluoromethyldehydroxylation of benzyl alcohols using the copper-dibromodifluoromethane-amide reaction system, although the yields are low.The mechanism of the reaction may involve chelation of the substrate to copper so that α-substituted benzyl alcohols and other alcohols are unreactive.

Reaction of Bis(heptafluorobutyryl) Peroxide with Carbanions and a Thiolate Anion

Yoshida, Masato,Shimokoshi, Kazuaki,Kobayashi, Michio

, p. 433 - 436 (2007/10/02)

In the reaction of bis(heptafluorobutyryl) peroxide with carbanions and a thiolate anion, two types of reactions were observed; one is an electron transfer reaction to give perfluoropropylated compounds and the other is a nucleophilic substitution.

Perfluoroalkylations of Carbanions with (Perfluoroalkyl)-phenyliodonium Triflates (FITS Reagents)

Umemoto, Teruo,Gotoh, Yoshihiko

, p. 439 - 446 (2007/10/02)

FITS reagents reacted with primary alkylmagnesium halides in THF at -78 deg C to give the corresponding perfluoroalkyl(Rf)-alkanes in moderate to good yields.But an alkyl-lithium or -copper gave a poor yield of the Rf-product.The rea

PERFLUOROALKYLATION OF CARBANIONS

Umemoto, Teruo,Kuriu, Yuriko

, p. 5197 - 5200 (2007/10/02)

A successful perfluoroalkylation of various carbanions by the use of perfluoroalkylphenyliodonium trifluoromethanesulfonate (FITS) was described.The reactivity of other perfluoroalkyliodonium salt was also examined.

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