Buy 3-Methoxymorphinan Cas 1531-25-5

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Buy 3-Methoxymorphinan Cas 1531-25-5

Buy 3-Methoxymorphinan Cas 1531-25-5

3-Methoxymorphinan is an inactive metabolite of both dextromethorphan and levomethorphan, and has been shown to produce local anesthetic effects.[1] It is the CYP3A4 metabolite of the aforementioned drugs,[2] and is itself metabolized by the liver enzyme CYP2D6.[3]

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Cost-effective and customizable 3-METHOXYMORPHINAN HCL 1531-25-5 in stock

  • Molecular Formula:C17H23 N O
  • Molecular Weight:257.376
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:403.2°Cat760mmHg 
  • Flash Point:167.1°C 
  • PSA:21.26000 
  • Density:1.12g/cm3 
  • LogP:3.37000 

3-METHOXYMORPHINAN HCL(Cas 1531-25-5) Usage

General Description 3-Methoxymorphinan HCl, or 3-Methoxy-N-methyl-morphinan hydrochloride, is a chemical derived from the morphinan group of opioids, which includes drugs like morphine. It is typically used for research purposes, especially in the study of the human body’s reaction to opioids and potential treatments for opioid addiction. Its chemical formula is C18H24NO2·HCl, it contains 22.07% nitrogen, 6.96% hydrogen, and 30.64% chlorine in its molecular composition. Not intended for human consumption, it must be handled with care due to its potential toxicity and it falls under the category of controlled substances in many jurisdictions.

InChI:InChI=1/C17H23NO/c1-19-13-6-5-12-10-16-14-4-2-3-7-17(14,8-9-18-16)15(12)11-13/h5-6,11,14,16,18H,2-4,7-10H2,1H3/t14-,16+,17+/m0/s1

1531-25-5 Relevant articles

N-demethylation of dextromethorphan

Peet

, p. 1447 – 1448 (1980)

–

ANALOGS OF DEXTROMETHORPHAN WITH BALANCED RECEPTOR ACTIVITIES

–

Paragraph 0073-0075, (2022/03/09)

Substituted analogs of dextromethorphan …

Late-Stage Conversion of a Metabolically Labile Aryl Methyl Ether-Containing Natural Product to Fluoroalkyl Analogues

Altman, Ryan A.,Ambler, Brett R.,Sorrentino, Jacob P.

, p. 5416 – 5427 (2020/05/19)

We report the conversion of aryl methyl …

CYP2D6 allelic variants *34, *17-2, *17-3, and *53 and a Thr309Ala mutant display altered kinetics and NADPH coupling in metabolism of bufuralol and dextromethorphan and altered susceptibility to inactivation by SCH 66712

Glass, Sarah M.,Martell, Cydney M.,Oswalt, Alexandria K.,Osorio-Vasquez, Victoria,Cho, Christi,Hicks, Michael J.,Mills, Jacqueline M.,Fujiwara, Rina,Glista, Michael J.,Kamath, Sharat S.

supporting information, p. 1106 – 1117 (2018/08/12)

Metabolic phenotype can be affected by m…

COMPOSITIONS AND METHODS THEREOF

–

Paragraph 00535, (2018/03/25)

Compounds of formula I, (I) or enantiome…

1531-25-5 Process route

levomethorphan
125-70-2,1453167-99-1levomethorphan
(-)-3-Methoxymorphinan
1531-25-5(-)-3-Methoxymorphinan
Conditions

Conditions Yield
levomethorphan; With carbonochloridic acid 1-chloro-ethyl ester; sodium hydrogencarbonate; In 1,2-dichloro-ethane; for 48h; Heating;
With methanol; for 3h; Further stages.; Heating;
90%
levomethorphan; With bromocyane; In dichloromethane; Inert atmosphere; Reflux;
With potassium hydroxide; In diethylene glycol; at 160 ℃; for 2h;
85%
levomethorphan; With carbonochloridic acid 1-chloro-ethyl ester;
With methanol;
With carbonochloridic acid 1-chloro-ethyl ester; potassium carbonate; In 1,2-dichloro-ethane; for 6h; Heating;
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