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(2R,6S)-2-(3,4-dimethoxyphenyl)-6-(4-methoxyphenethyl)tetrahydro-2H-pyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1451998-94-9

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1451998-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1451998-94-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,9,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1451998-94:
(9*1)+(8*4)+(7*5)+(6*1)+(5*9)+(4*9)+(3*8)+(2*9)+(1*4)=209
209 % 10 = 9
So 1451998-94-9 is a valid CAS Registry Number.

1451998-94-9Downstream Products

1451998-94-9Relevant academic research and scientific papers

Catalytic δ-hydroxyalkynone rearrangement in the stereoselective total synthesis of centrolobine, engelheptanoxides A and C and analogues

Ahmad, Mohammad N.,Chopra, Sidharth,Fernandes, Rodney A.,Kumar, Praveen

, (2021/08/13)

A catalytic stereoselective total synthesis of centrolobine and engelheptanoxides A and C has been completed via a metal-free catalytic δ-hydroxyalkynone rearrangement to 2,3-dihydro-4H-pyran-4-one and diastereoselective hydrogenation to the all syn-2,4,6-trisubstituted pyran strategy. The onliest required chirality was introduced by Jacobsen kinetic resolution, which further directed the diastereoselective hydrogenation. A first stereoselective synthesis of engelheptanoxide A is also accomplished. The analogues and derivatives of centrolobine and engelheptanoxides prepared were evaluated for antitubercular activity against M. tuberculosis H37Rv ATCC 27294.

Synthesis of (+)-centrolobine and its analogues by using acyl anion chemistry

Sudarshan, Kasireddy,Aidhen, Indrapal Singh

, p. 2298 - 2302 (2013/05/09)

A new route based on the use of acyl anion chemistry was developed for the synthesis of (+)-centrolobine and its analogues. Acid-catalyzed benzylic cation initiated cyclization was the key step in the stereoselective formation of the cis-2,6-disubstituted tetrahydropyran ring. The developed methodology was applied to the synthesis of (+)-centrolobine analogues containing electron-donating substituents in the aryl rings.

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