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(9S)-3,10-Didehydro-10,11-dihydrocinchonan-9-ol is a complex organic compound with the molecular formula C20H23NO2. It is a derivative of the naturally occurring alkaloid quinine, which is found in the bark of the cinchona tree. This specific compound is characterized by its unique structure, featuring a dehydrogenated ring system and a hydroxyl group at the 9-position. It is known for its potential applications in the pharmaceutical industry, particularly in the development of antimalarial drugs, due to its structural similarity to quinine. The compound's stereochemistry, with the 9-hydroxyl group in the S-configuration, is crucial for its biological activity. Research on such compounds is important for understanding their potential therapeutic effects and for the design of new drugs targeting various diseases.

6874-76-6

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6874-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6874-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6874-76:
(6*6)+(5*8)+(4*7)+(3*4)+(2*7)+(1*6)=136
136 % 10 = 6
So 6874-76-6 is a valid CAS Registry Number.

6874-76-6Upstream product

6874-76-6Downstream Products

6874-76-6Relevant academic research and scientific papers

Hydrogenation of prochiral ketones

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Page/Page column 5-6, (2010/01/31)

Process for enantioselectively hydrogenating prochiralen ketones to (S)-alcohols using platinum catalysts in the presence of cinchonines or quinidines as modifiers and in the presence of hydrogen, which is characterized in that the modifiers used are cinchonines unsubstituted in the 3-position, 3-ethylidenyl- or 9-methoxycinchonines or derivatives thereof in which the quinoline ring is replaced by other rings.

Hydrogenation of prochiral ketones

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Page/Page column 9, (2010/11/29)

Process for enantioselectively hydrogenating prochiralen ketones to (S)-alcohols using platinum catalysts in the presence of cinchonines or quinidines as modifiers and in the presence of hydrogen, which is characterized in that the modifiers used are cinchonines unsubstituted in the 3-position, 3-ethylidenyl- or 9-methoxycinchonines or derivatives thereof in which the quinoline ring is replaced by other rings.

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