113951-05-6 Usage
Description
rac-(17Ξ)-3-methoxy-17-methyl-morphinane-17-oxide is a chemical compound with the molecular formula C18H21NO3. It is a derivative of morphine and belongs to the class of morphinane alkaloids. rac-(17Ξ)-3-methoxy-17-methyl-morphinane-17-oxide has a complex structure, containing a morphine core with a methoxy group and a methyl group attached at specific positions, as well as an oxide functional group. It possesses analgesic properties and is related to the opioid receptor agonist activity of morphine. rac-(17Ξ)-3-methoxy-17-methyl-morphinane-17-oxide has potential pharmaceutical applications for pain management and may also have implications for research in the field of opioid pharmacology.
Uses
Used in Pharmaceutical Industry:
rac-(17Ξ)-3-methoxy-17-methyl-morphinane-17-oxide is used as an analgesic agent for its pain-relieving properties. Its relation to the opioid receptor agonist activity of morphine makes it a potential candidate for the development of new pain management therapies.
Used in Research and Development:
rac-(17Ξ)-3-methoxy-17-methyl-morphinane-17-oxide is used as a research compound for studying the mechanisms of opioid pharmacology. Its complex structure and potential applications in pain management make it a valuable tool for scientists working on the development of novel therapeutic strategies for various types of pain.
Check Digit Verification of cas no
The CAS Registry Mumber 113951-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,9,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113951-05:
(8*1)+(7*1)+(6*3)+(5*9)+(4*5)+(3*1)+(2*0)+(1*5)=106
106 % 10 = 6
So 113951-05-6 is a valid CAS Registry Number.
113951-05-6Relevant articles and documents
Selectivities in the oxidation of tertiary amines and pyridine derivatives by perfluoro cis-2,3-dialkyloxaziridines
Arnone, Alberto,Metrangolo, Pierangelo,Novo, Barbara,Resnati, Giuseppe
, p. 7831 - 7842 (1998)
When tertiary amines 1 are reacted with perfluoro cis-2,3- dialkyloxaziridines 2 at -60 °C corresponding N-oxides 3 are formed in high yields. The process is chemoselective and diastereoselective. The chemoselectivity in the reaction of alkenyl substituted pyridines is solvent dependent, attack occurring exclusively at the carbon-carbon double bond or at the nitrogen atom under protic and aprotic conditions, respectively. Lower selectivities were obtained when standard reagents were used.
Preparation method of dextromethorphan hydrobromide oxynitride impurity (by machine translation)
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Paragraph 0031-0044, (2019/08/30)
The invention discloses a preparation method of a compound represented by dextromethorphan hydrobromide impurity type I. The dextromethorphan hydrobromide impurity type I preparation method comprises the following steps: dissolving dextromethorphan hydrobromide in water, carrying out free extraction with a base, extracting, and reacting under the action of an oxidizing agent by using an organic solvent to obtain the compound . the method comprises the following steps: dissolving dextromethorphan hydrobromide in water. The preparation method is convenient to operate, mild and controllable in reaction conditions, high in reaction stability, high in reaction product yield, and high in purity. (by machine translation)
