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(E)-1-(3-methyl)phenyl-2-(3-pyridyl)ethene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24483-33-8

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24483-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24483-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,8 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24483-33:
(7*2)+(6*4)+(5*4)+(4*8)+(3*3)+(2*3)+(1*3)=108
108 % 10 = 8
So 24483-33-8 is a valid CAS Registry Number.

24483-33-8Downstream Products

24483-33-8Relevant academic research and scientific papers

Stereospecific hydrodehalogenation of alkenyl bromides: A new approach to the synthesis of (E)-alkenes

Chelucci, Giorgio

, p. 4069 - 4072 (2014/04/03)

The pair NaBH4-TMEDA and catalytic PdCl2(PPh 3)2 in THF at room temperature is a mild and efficient system for the hydrodebromination of alkenyl bromides, providing a facile reduction procedure that allows completing the process advantageously, leading from aldehydes to (E)-alkenes. This journal is the Partner Organisations 2014.

Diversity-oriented synthesis of multisubstituted olefins through the sequential integration of palladium-catalyzed cross-coupling reactions. 2-Pyridyldimethyl(vinyl)silane as a versatile platform for olefin synthesis

Itami,Nokami,Ishimura,Mitsudo,Kamei,Yoshida

, p. 11577 - 11585 (2007/10/03)

A novel strategy for the diversity-oriented synthesis of multisubstituted olefins, where 2-pyridyldimethyl (vinyl)silane functions as a versatile platform for olefin synthesis, is described. The palladium-catalyzed Heck-type coupling of 2-pyridyldimethyl(vinyl)silanes with organic iodides took place in the presence of Pd2-(dba) 3/tri-2-furylphosphine catalyst to give β-substituted vinylsilanes in excellent yields. The Heck-type coupling occurred even with α- and β-substituted 2-pyridyldimethyl(vinyl)silanes. The one-pot double Heck coupling of 2-pyridyldimethyl(vinyl)silane took place with two different aryl iodides to afford β,β-diarylated vinylsilanes in good yields. The palladium-catalyzed Hiyama-type coupling of 2-pyridyldimethyl(vinyl)silane with organic halides took place in the presence of tetrabutylammonium fluoride to give di- and trisubstituted olefins in high yields. The sequential integration of Heck-type (or double Heck) coupling and Hiyama-type coupling produced the multisubstituted olefins in regioselective, stereoselective, and diversity-oriented fashions. Especially, the one-pot sequential Heck/Hiyama coupling reaction provides an extremely facile entry into a diverse range of stereodefined multisubstituted olefins. Mechanistic considerations of both Heck-type and Hiyama-type coupling reactions are also described.

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