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(4S,2Z)-pentafluorophenyl 4-tert-butyldimethylsilyloxypent-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

167281-07-4

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167281-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167281-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,2,8 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167281-07:
(8*1)+(7*6)+(6*7)+(5*2)+(4*8)+(3*1)+(2*0)+(1*7)=144
144 % 10 = 4
So 167281-07-4 is a valid CAS Registry Number.

167281-07-4Relevant academic research and scientific papers

Internal Activation of Acrylate-Type Dienophiles in Diels-Alder Reactions

Kan, Toshiyuki,Ohfune, Yasufumi

, p. 943 - 946 (1995)

Diels-Alder reactions of less reactive acrylate-type dienophiles with dienes were achieved by replacing its ester counterpart to a pentafluorophenyl group, which remarkably enhanced the reactivity of the dienophiles to give the corresponding cycloadducts

Internal activation of acrylate-type dienophiles for the diels-alder reaction. Stereoselective synthesis of conformationally constrained glutamate analogs

Ohfune, Yasufumi,Kan, Toshiyuki,Nakajima, Terumi

, p. 5207 - 5224 (2007/10/03)

The [4+2] cycloaddition reaction of the unreactive acrylate-type dienophiles such as 5a and 6a was accomplished by introducing an electronegative or electron-withdrawing group as the ester counterpart. Among them, the pentafluorophenyl (PFP) group was found to be an excellent ester counterpart in view of its rate acceleration and chemical stability under the reaction conditions. The 13C NMR spectral data of the dienophiles with the PFP group suggested that the conjugated CC-double bond was strongly polarized. The internal activation was found to be effective for the related dienophile or other dienes, in particular, unstable to Lewis acid catalysts. A successful application of this method is demonstrated by the syntheses of conformationally restricted analogs of L-glutamate, 3 and 4.

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