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51356-54-8

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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

51356-54-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[dimethylamino-(3-methoxyphenyl)methyl]cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names EINECS 257-150-7

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51356-54-8 SDS

51356-54-8Upstream product

51356-54-8Downstream Products

51356-54-8Relevant articles and documents

Benzylamine analgesics

-

, (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.

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