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(E)-2-Phenyl-hex-2-enoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78427-50-6

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78427-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78427-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,2 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78427-50:
(7*7)+(6*8)+(5*4)+(4*2)+(3*7)+(2*5)+(1*0)=156
156 % 10 = 6
So 78427-50-6 is a valid CAS Registry Number.

78427-50-6Downstream Products

78427-50-6Relevant academic research and scientific papers

Titanium-mediated carboxylation of alkynes with carbon dioxide

Six, Yvan

, p. 1157 - 1171 (2003)

The regioselective carboxylation of nonactivated internal alkynes can be performed with carbon dioxide under atmospheric pressure using a simple procedure based on the chemistry of Sato-type diisopropyloxytitanacyclopropenes. Various polysubstituted vinylcarboxylic acids and butenolides can be prepared in this way. In addition, this paper describes an experimental protocol for the preparation of solutions of (η2-cyclopentene)diisopropyloxytitanium. This complex also reacts with carbon dioxide, and mediates pinacol coupling of acetophenone. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

A Simple and Efficient Route to 2-Alkyl-2-alkenoic Acids and 2-Phenyl-2-Alkenoic Acids by the Horner Synthesis. Application to the Steroselective Synthesis of the Pheromone Manicone

Coutrot, Philippe,Ghribi, Abdellaziz

, p. 790 - 792 (2007/10/02)

A general synthesis of α-branched α,β-unsaturated carboxylic acids is described.A Horner reaction of 2-diethoxyphosphorylalkanoic acid dianions (lithium α-lithiocarboxylates) with carbonyl compounds is used.The reaction is applied to the stereoselective synthesis of Manicone.

Structural Effects of the Acidity of E-α-Phenyl-β-arylacrilic Acids

Maccarone, Emanuele,Mamo, Antonino,Perrini, Giancarlo,Torre, Michele

, p. 395 - 398 (2007/10/02)

The dissociation equilibrium constants of some E-α-phenyl-β-arylacrilic acids (Ar=2-pyridyl, 3-pyridyl, 4-pyridyl, 1-naphthyl, 2-naphthyl, anthracen-9-yl) have been measured in 80percent aqeous 2-methoxyethanol at 25 deg C., The pKa values of these acids, together with those of p-substituted phenyl, 2-furyl, 2-thienyl and selenophen-2-yl derivitives, have been rationalized by an equation involving separate contributions of polar, conjugative and steric effects of heterocycles.The pKa values of some E-α-phenyl-β-alkylacrilic acids (alk=methyl; ethyl; n-propyl; i-propyl; n-butyl; i-butyl) are also reported.

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