Methoxetamine hydrochloride solution

Base Information

• Chemical Name: Methoxetamine hydrochloride solution
• CAS No.: 1239908-48-5
• Molecular Formula: C₁₅H₂₁NO₂*ClH
• Molecular Weight: 283.798
• Mol file: 1239908-48-5.mol

Synonyms:Methoxetamine (hydrochloride);Methoxetamine hydrochloride solution;2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone hydrochloride;2-(ethylamino)-2-(3-methoxyphenyl)cyclohexan-1-one:hydrochloride

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of Methoxetamine hydrochloride solution

Chemical Property:

• Flash Point: 9℃
• PSA: 38.33000
• LogP: 3.83600
• Storage Temp.: ?20°C

Purity/Quality:

Safty Information:

• Pictogram(s): F,T
• Hazard Codes: F,T
• Statements: 11-23/24/25-39/23/24/25
• Safety Statements: 7-16-36/37-45

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: Methoxetamine hydrochloride solution, a chemical compound, has limited applications primarily in the field of research and academia. It is a dissociative anesthetic and hallucinogenic compound, and as such, it is not approved for medical or therapeutic use in humans. However, it is utilized in laboratory research, particularly in the study of the NMDA receptor and its effects on the central nervous system. Researchers may use it to gain insights into the mechanisms of action of dissociative drugs and their potential impact on brain function. Despite its restricted use and lack of approved applications in other fields, its role in scientific research is pivotal for advancing our understanding of neuropharmacology and the effects of certain substances on the brain.

Technology Process of Methoxetamine hydrochloride solution

There total 8 articles about Methoxetamine hydrochloride solution which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(S)-(+)-methoxetamine (+)-O,O'-di-p-toluoyl-D-tartarate → (S)-(+)-methoxetamine hydrochloride (1239908-48-5)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / water

2: hydrogenchloride / methanol / 0 °C

With hydrogenchloride; sodium hydrogencarbonate; In methanol; water;

DOI:10.1039/d0nj05192f

Reference yield:

1-((Ethylimino)(3-methoxyphenyl) methyl)cyclopentan-1-ol → methoxetamine hydrochloride (1239908-48-5)

Guidance literature:

Multi-step reaction with 2 steps

1: palladium dichloride / decalin / 10 h / Sealed tube; Heating

2: hydrogenchloride / methanol

With hydrogenchloride; palladium dichloride; In methanol; decalin;

DOI:10.1039/d0nj05192f

Reference yield:

3-methoxybenzonitrile (1527-89-5) → methoxetamine hydrochloride (1239908-48-5)

Guidance literature:

Multi-step reaction with 5 steps

1: diethyl ether / 6 h / 0 - 20 °C / Inert atmosphere

2: copper(ll) bromide / ethyl acetate / 4 h / Reflux

3: 18 h / -40 - 20 °C / Sealed tube; Inert atmosphere

4: palladium dichloride / decalin / 10 h / Sealed tube; Heating

5: hydrogenchloride / methanol

With hydrogenchloride; copper(ll) bromide; palladium dichloride; In methanol; diethyl ether; ethyl acetate; decalin;

DOI:10.1039/d0nj05192f

upstream raw materials:

3-methoxybenzonitrile

(m-methoxyphenyl)cyclopentyl ketone

(±)-2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone