ChemSpider 2D Image | Tramadol hydrochloride | C16H26ClNO2

Tramadol hydrochloride

  • Molecular FormulaC16H26ClNO2
  • Average mass299.836 Da
  • Monoisotopic mass299.165222 Da
  • ChemSpider ID56711

  • defined stereocentres - 2 of 2 defined stereocentres

More details:

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

(+)-tramadol hydrochloride
(±)-cis-2-(Dimethylaminomethyl)-1-(3-methoxyphenyl)cyclohexanol hydrochloride
(1R,2R)-2-[(diméthylamino)méthyl]-1-(3-méthoxyphényl)cyclohexanol chlorhydrate
(1R,2R)-2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride
(1R,2R)-2-[(Dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride (1:1) [ACD/IUPAC Name]
(1R,2R)-2-[(Diméthylamino)méthyl]-1-(3-méthoxyphényl)cyclohexanol, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
(1R,2R)-2-[(Dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanolhydrochlorid [German]
(1R,2R)-2-[(Dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanolhydrochlorid (1:1) [German] [ACD/IUPAC Name]
22204-88-2 [RN]
252-950-2 [EINECS]
More...

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

42965_FLUKA [DBID]
CG 315 [DBID]
D01355 [DBID]
HSDB 7047 [DBID]
UC456_SIGMA [DBID]
  • Miscellaneous

    • Chemical Class:

      A hydrochloride resulting from the reaction of (<stereo>R</stereo>,<stereo>R</stereo>)-tramadol with 1 molar equivalent of hydrogen chloride; the (<stereo>R</stereo>,<stereo>R</stereo>)-enantiomer of the racemic opioid analgesic tramadol hydrochloride, it exhibits ten-fold higher analgesic potency than the (<stereo>S</stereo>,<stereo>S</stereo>)-enantiomer. ChEBI CHEBI:75733
      A hydrochloride resulting from the reaction of (R,R)-tramadol with 1 molar equivalent of hydrogen chloride; the (R,R)-enantiomer of ; the racemic opioid analgesic tramadol hydrochloride, it exhibits t en-fold higher analgesic potency than the (S,S)-enantiomer. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:75733
      A hydrochloride resulting from the reaction of (R,R)-tramadol with 1 molar equivalent of hydrogen chloride; the (R,R)-enantiomer of the racemic opioid analgesic tramadol hydrochloride, it exhibits ten -fold higher analgesic potency than the (S,S)-enantiomer. ChEBI CHEBI:75733

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

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site


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