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(-)-5-m-hydroxyphenyl-2-methylmorphan, also known as levomethorphan, is a potent opioid analgesic derived from the morphinan class. Structurally similar to morphine, it exhibits greater potency and fewer side effects, making it a valuable pharmaceutical compound for pain management.
Used in Pharmaceutical Industry:
(-)-5-m-hydroxyphenyl-2-methylmorphan is used as an analgesic agent for the treatment of moderate to severe pain. It functions by binding to opioid receptors in the brain and spinal cord, effectively inhibiting pain sensation and providing relief.
Used in Pain Management:
(-)-5-m-hydroxyphenyl-2-methylmorphan is used as a central nervous system depressant to alleviate pain. Due to its high potency and relatively lower side effects compared to other opioids, it is a preferred choice for managing various types of pain under medical supervision.
Used in Medical Supervision:
(-)-5-m-hydroxyphenyl-2-methylmorphan is used with caution and under close medical supervision due to its potential for addiction, tolerance, and respiratory depression. This ensures that patients receive the necessary pain relief while minimizing the risks associated with opioid use.

28623-84-9

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28623-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28623-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,2 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28623-84:
(7*2)+(6*8)+(5*6)+(4*2)+(3*3)+(2*8)+(1*4)=129
129 % 10 = 9
So 28623-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO/c1-16-9-8-15(7-3-5-13(16)11-15)12-4-2-6-14(17)10-12/h2,4,6,10,13,17H,3,5,7-9,11H2,1H3/t13-,15+/m1/s1

28623-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(1R,5S)-2-methyl-2-azabicyclo[3.3.1]nonan-5-yl]phenol

1.2 Other means of identification

Product number -
Other names -

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

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

More Details:28623-84-9 SDS

28623-84-9Relevant academic research and scientific papers

Opioid ligands with mixed properties from substituted enantiomeric N-phenethyl-5-phenylmorphans. Synthesis of a -agonist δ-antagonist and δ-inverse agonists

Cheng, Kejun,Kim, In Jong,Lee, Mei-Jing,Adah, Steven A.,Raymond, Tyler J.,Bilsky, Edward J.,Aceto, Mario D.,May, Everette L.,Harris, Louis S.,Coop, Andrew,Dersch, Christina M.,Rothman, Richard B.,Jacobson, Arthur E.,Rice, Kenner C.

, p. 1177 - 1190 (2008/02/04)

Enantiomeric N-phenethyl-m-hydroxyphenylmorphans with various substituents in the ortho, meta or para positions of the aromatic ring in the phenethylamine side-chain (chloro, hydroxy, methoxy, nitro, methyl), as well as a pyridylethyl and a indolylethyl m

A Marked Change of Receptor Affinity of the 2-Methyl-5-(3-hydroxyphenyl)morphans upon Attachment of an (E)-8-Benzylidene Moiety: Synthesis and Evaluation of a New Class of ? Receptor Ligands

Bertha, Craig M.,Mattson, Mariena V.,Flippen-Anderson, Judith L.,Rothman, Richard B.,Xu, Heng,et al.

, p. 3163 - 3170 (2007/10/02)

The (E)-8-benzylidene and (E)-8-(3,4-dichlorobenzylidene), 7-ketone derivatives, 5 and 6, of the synthetic opiate 2-methyl-5-(3-hydroxyphenyl)morphan nonane, 1>, were synthesized from the 7-ketone derivativ

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