51356-54-8 Usage
Classification
Synthetic opioid analgesic drug
Chemical Structure
2-[(dimethylamino)(3-methoxyphenyl)methyl]cyclohexan-1-ol
Mechanism of Action
Acts as a potent agonist at the μ-opioid receptor
Similarity to Morphine and Heroin
Chemically related to morphine and heroin
Effects
Similar effects to other morphinans such as levorphanol, dextromethorphan, and dextrorphan
Medical Uses
Treatment of moderate to severe pain
Antitussive effects in cough suppressants
Regulatory Status
Considered a controlled substance in many countries due to potential for abuse and addiction
Side Effects
Drowsiness
Constipation
Respiratory depression
Check Digit Verification of cas no
The CAS Registry Mumber 51356-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,5 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51356-54:
(7*5)+(6*1)+(5*3)+(4*5)+(3*6)+(2*5)+(1*4)=108
108 % 10 = 8
So 51356-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H25NO2/c1-17(2)16(14-9-4-5-10-15(14)18)12-7-6-8-13(11-12)19-3/h6-8,11,14-16,18H,4-5,9-10H2,1-3H3
51356-54-8Relevant articles and documents
Benzylamine analgesics
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, (2008/06/13)
Reaction of benzalcyclanones with secondary amines affords aminobenzylcyclohexanones, which, upon reduction, yield aminobenzylcyclohexanols having potent analgesic activity. Epimeric aminobenzylcycloalkanols having analgesic activity are prepared by the reaction of C-phenyl nitrones with cycloalkenes to form benzisoxazoles, treatment with alkyl halide to form the corresponding benzisoxazolium halides, followed by hydrogenolysis.
