ChemSpider 2D Image | (S,S)-tramadol hydrochloride | C16H26ClNO2

(S,S)-tramadol hydrochloride

  • Molecular FormulaC16H26ClNO2
  • Average mass299.836 Da
  • Monoisotopic mass299.165222 Da
  • ChemSpider ID8193224
  • defined stereocentres - 2 of 2 defined stereocentres


More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

(±)-cis-2-((Dimethylamino)methyl)-1-(3-methoxyphenyl)cyclohexanol hydrochloride
(±)-cis-2-((Dimethylamino)methyl)-1-(m-methoxyphenyl)cyclohexanol hydrochloride
(1S,2S)-2-[(Dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride (1:1) [ACD/IUPAC Name]
(1S,2S)-2-[(Diméthylamino)méthyl]-1-(3-méthoxyphényl)cyclohexanol, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
(1S,2S)-2-[(Dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanolhydrochlorid (1:1) [German] [ACD/IUPAC Name]
(S,S)-tramadol hydrochloride
Cyclohexanol, 2-((dimethylamino)methyl)-1-(3-methoxyphenyl)-, hydrochloride, cis-
Cyclohexanol, 2-((dimethylamino)methyl)-1-(3-methoxyphenyl)-, hydrochloride, cis-( -)-
Cyclohexanol, 2-((dimethylamino)methyl)-1-(m-methoxyphenyl)-, hydrochloride, cis-(±)-
Cyclohexanol, 2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)-, (1S,2S)-, hydrochloride (1:1) [ACD/Index Name]
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  • Miscellaneous
    • Chemical Class:

      A hydrochloride resulting from the reaction of (<stereo>S</stereo>,<stereo>S</stereo>)-tramadol with 1 molar equivalent of hydrogen chloride; the (<stereo>S</stereo>,<stereo>S</stereo>)-enantiomer of the racemic opioid analgesic tramadol hydrochloride, it exhibits ten-fold lower analgesic potency than the (<stereo>R</stereo>,<stereo>R</stereo>)-enantiomer. ChEBI CHEBI:75734
      A hydrochloride resulting from the reaction of (S,S)-tramadol with 1 molar equivalent of hydrogen chloride; the (S,S)-enantiomer of ; the racemic opioid analgesic tramadol hydrochloride, it exhibits t en-fold lower analgesic potency than the (R,R)-enantiomer. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:75734
      A hydrochloride resulting from the reaction of (S,S)-tramadol with 1 molar equivalent of hydrogen chloride; the (S,S)-enantiomer of the racemic opioid analgesic tramadol hydrochloride, it exhibits ten -fold lower analgesic potency than the (R,R)-enantiomer. ChEBI CHEBI:75734

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

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