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(3S,4R)-3-((benzo[d][1,3]dioxol-5-yloxy)methyl)-1-methyl-4-phenylpiperidine is a chiral piperidine derivative with a molecular formula of C23H27NO3 and a molecular weight of 377.47 g/mol. It features a piperidine ring, a benzodioxole ring, and a phenyl group, and is characterized by its (3S,4R) configuration.

324023-99-6

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324023-99-6 Usage

Uses

Used in Organic Synthesis:
(3S,4R)-3-((benzo[d][1,3]dioxol-5-yloxy)methyl)-1-methyl-4-phenylpiperidine is used as a building block in organic synthesis for the development of novel compounds with potential applications in various fields.
Used in Medicinal Chemistry Research:
(3S,4R)-3-((benzo[d][1,3]dioxol-5-yloxy)methyl)-1-methyl-4-phenylpiperidine is used as a key intermediate in medicinal chemistry research to explore its potential as a therapeutic agent.
Used in Pharmaceutical Development:
While further studies are needed to determine its specific biological activities, (3S,4R)-3-((benzo[d][1,3]dioxol-5-yloxy)methyl)-1-methyl-4-phenylpiperidine may have potential pharmacological and therapeutic applications, making it a candidate for pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 324023-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,0,2 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 324023-99:
(8*3)+(7*2)+(6*4)+(5*0)+(4*2)+(3*3)+(2*9)+(1*9)=106
106 % 10 = 6
So 324023-99-6 is a valid CAS Registry Number.

324023-99-6Relevant academic research and scientific papers

Synthesis and 5HT modulating activity of stereoisomers of 3-phenoxymethyl-4-phenylpiperidines

Engelstoft, Mogens,Hansen, John Bondo

, p. 164 - 169 (2007/10/03)

A series of pairs of enantiomers of substituted 3-phenoxymethyl-4-phenylpiperidines has been prepared from arecoline or α-methylstyrene by a combination of stereospecific reactions and optical resolutions. The ability of the compounds to modulate serotonin (5HT) neurotransmission in vitro was determined. Several derivatives, among which is the antidepressant paroxetine, are very potent inhibitors of 5HT reuptake. These compounds exhibit a pronounced steric requirement for inhibition of 5HT reuptake and binding to 5HT2A and 5HT2C receptors. Acta Chemica Scandinavica 1996.

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