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(E)-2-(1-phenylprop-1-en-2-yl)pyridine is an organic compound characterized by a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a 1-phenylprop-1-en-2-yl group, which is a phenylpropene moiety with a double bond between the first and second carbon atoms. (E)-2-(1-phenylprop-1-en-2-yl)pyridine is a conjugated system, meaning that the π electrons are delocalized across the molecule, which can influence its chemical reactivity and physical properties. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential to form stable complexes with metal ions. The compound's structure and properties make it a valuable intermediate in organic synthesis, particularly in the preparation of compounds with potential biological activity.

23847-63-4

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23847-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23847-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,4 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23847-63:
(7*2)+(6*3)+(5*8)+(4*4)+(3*7)+(2*6)+(1*3)=124
124 % 10 = 4
So 23847-63-4 is a valid CAS Registry Number.

23847-63-4Relevant academic research and scientific papers

Iron-catalyzed stereospecific activation of olefinic C-H bonds with grignard reagent for synthesis of substituted olefins

Ilies, Laurean,Asako, Sobi,Nakamura, Eiichi

supporting information; experimental part, p. 7672 - 7675 (2011/06/26)

The reaction of an aryl Grignard reagent with a cyclic or acyclic olefin possessing a directing group such as pyridine or imine results in the stereospecific substitution of the olefinic C-H bond syn to the directing group. The reaction takes place smoothly and without isomerization of the product olefin in the presence of a mild oxidant (1,2-dichloro-2-methylpropane) and an aromatic cosolvent. Several lines of evidence suggest that the reaction proceeds via iron-catalyzed olefinic C-H bond activation rather than an oxidative Mizoroki-Heck-type reaction.

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