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[(3R,4R)-4-(4-Fluoro-phenyl)-piperidin-3-yl]-methanol is a chiral piperidine derivative featuring a fluorophenyl group attached to the piperidine ring and a hydroxyl functional group from the methanol moiety. Its (3R,4R) configuration indicates the presence of four stereoisomers, suggesting potential pharmacological or biological applications due to the common use of piperidine derivatives in the synthesis of pharmaceuticals and agrochemicals. The fluorophenyl group may also provide specific properties or interactions with biological targets, making [(3R,4R)-4-(4-Fluoro-phenyl)-piperidin-3-yl]-methanol a promising candidate for further study in medicinal chemistry and drug development.

872544-48-4

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872544-48-4 Usage

Uses

Used in Pharmaceutical Industry:
[(3R,4R)-4-(4-Fluoro-phenyl)-piperidin-3-yl]-methanol is used as a building block for the synthesis of various pharmaceuticals due to its piperidine derivative nature and the potential for specific interactions conferred by the fluorophenyl group. Its chiral configuration may offer selectivity in targeting biological receptors or enzymes, leading to more effective and selective medications.
Used in Agrochemical Industry:
In the agrochemical industry, [(3R,4R)-4-(4-Fluoro-phenyl)-piperidin-3-yl]-methanol is used as a key component in the development of new pesticides or herbicides. The fluorophenyl group may provide unique properties that enhance the compound's effectiveness in targeting specific pests or weeds, while the chiral center could offer selectivity in biological activity, reducing potential harm to non-target organisms.
Used in Medicinal Chemistry Research:
[(3R,4R)-4-(4-Fluoro-phenyl)-piperidin-3-yl]-methanol is utilized as a subject of study in medicinal chemistry research to explore its potential as a lead compound for the development of new drugs. [(3R,4R)-4-(4-Fluoro-phenyl)-piperidin-3-yl]-methanol's structure, including the fluorophenyl group and chiral center, may offer insights into novel mechanisms of action or targeting strategies for therapeutic intervention.
Used in Drug Delivery Systems:
As a component in drug delivery systems, [(3R,4R)-4-(4-Fluoro-phenyl)-piperidin-3-yl]-methanol may be employed to improve the bioavailability, targeting, or release profile of therapeutic agents. Its unique structural features could be leveraged to enhance the performance of drug carriers or to facilitate the development of novel targeted drug delivery platforms.

Check Digit Verification of cas no

The CAS Registry Mumber 872544-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,5,4 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 872544-48:
(8*8)+(7*7)+(6*2)+(5*5)+(4*4)+(3*4)+(2*4)+(1*8)=194
194 % 10 = 4
So 872544-48-4 is a valid CAS Registry Number.

872544-48-4Downstream Products

872544-48-4Relevant academic research and scientific papers

A new route to 3,4-disubstituted piperidines: Formal synthesis of (-)-paroxetine and (+)-femoxetine

Yamada, Shinji,Jahan, Ishrat

, p. 8673 - 8676 (2007/10/03)

A new route to 3,4-disubstituted piperidines was developed using chiral 1,4-dihydropyridines as key intermediates, the synthetic utility of which was demonstrated by formal synthesis of (-)-paroxetine and (+)-femoxetine.

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