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CAS 112058-89-6

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4-(4-Fluorophenyl)-3-(4-methoxy-3-hydroxyphenoxymethyl)piperidine

Description:
4-(4-Fluorophenyl)-3-(4-methoxy-3-hydroxyphenoxymethyl)piperidine, with the CAS number 112058-89-6, is a chemical compound characterized by its complex structure, which includes a piperidine ring substituted with a fluorophenyl group and a phenoxymethyl moiety that features both methoxy and hydroxy functional groups. This compound is typically classified as an organic molecule and may exhibit properties such as moderate solubility in organic solvents, depending on the specific functional groups present. The presence of the fluorine atom can influence its electronic properties, potentially enhancing lipophilicity and affecting biological activity. The methoxy and hydroxy groups may contribute to hydrogen bonding capabilities, which can influence the compound's reactivity and interactions with biological targets. Such compounds are often studied for their potential pharmacological applications, particularly in the fields of medicinal chemistry and drug development, where modifications to the piperidine structure can lead to variations in activity and selectivity.
Formula:C19H22FNO3
InChI:InChI=1/C19H22FNO3/c1-23-19-7-6-16(10-18(19)22)24-12-14-11-21-9-8-17(14)13-2-4-15(20)5-3-13/h2-7,10,14,17,21-22H,8-9,11-12H2,1H3/t14-,17-/m0/s1
SMILES:COc1ccc(cc1O)OC[C@@H]1CNCC[C@H]1c1ccc(cc1)F
Synonyms:
  • Paroxetine metabolite A
  • 5-[[(3S,4R)-4-(4-Fluorophenyl)-3-piperidinyl]methoxy]-2-methoxyphenol
  • 4-(4-FLUOROPHENYL)-3-(4-METHOXY-3-HYDROXYPHENOXYMETHYL)PIPERIDINE
  • BRL 36583A
  • (Paroxetine Metabolite)
  • (-)-trans 4-(4-Fluorophenyl)-3-(3-hydroxy-4-MethoxyphenoxyMethyl) piperidine
  • Paroxetine Related Impurity
  • Phenol, 5-[[(3S,4R)-4-(4-fluorophenyl)-3-piperidinyl]methoxy]-2-methoxy-
  • Paroxetine 3-Hydroxy Metabolite
  • (3S-trans)-5-[[4-(4-Fluorophenyl)-3-piperidinyl]methoxy]-2-methoxyphenol
  • Paroxetine 3-Hydroxy Metabolite Hydrochloride
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