38969-65-2

Basic information

• Product Name: ()-1,2,3,4,5,6,7,8-octahydro-1-[(4-methoxyphenyl)methyl]-2-methylisoquinoline
• Synonyms: (1)-1,2,3,4,5,6,7,8-Octahydro-1-((4-methoxyphenyl)methyl)-2-methylisoquinoline; 1-(4-methoxybenzyl)-2-methyl-1,2,3,4,5,6,7,8-octahydroisoquinoline
• CAS NO: 38969-65-2
• Molecular Formula: C₁₈H₂₅NO
• Molecular Weight: 271.3972
• EINECS: 254-226-1
• Mol File: 38969-65-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 397.8°C at 760 mmHg
• Flash Point: 117°C
• Density: 1.06g/cm³
• Vapor Pressure: 1.55E-06mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: ()-1,2,3,4,5,6,7,8-octahydro-1-[(4-methoxyphenyl)methyl]-2-methylisoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: ()-1,2,3,4,5,6,7,8-octahydro-1-[(4-methoxyphenyl)methyl]-2-methylisoquinoline(38969-65-2)
• EPA Substance Registry System: ()-1,2,3,4,5,6,7,8-octahydro-1-[(4-methoxyphenyl)methyl]-2-methylisoquinoline(38969-65-2)

Safety Data

• Hazardous Substances Data: 38969-65-2(Hazardous Substances Data)

Usage

General Description

"()-1,2,3,4,5,6,7,8-octahydro-1-[(4-methoxyphenyl)methyl]-2-methylisoquinoline" is a chemical compound with a complex molecular structure. It is classified as an isoquinoline derivative, containing a central isoquinoline ring with a methyl group and a 4-methoxyphenylmethyl group attached to it. The compound also contains a series of eight hydrogen atoms, contributing to its octahydro prefix. This chemical may have potential pharmaceutical applications due to its structural features, but further research and testing would be needed to determine its specific properties and potential uses.

Upstream product

• 118646-97-2 1-(4-methoxy-benzyl)-2-methyl-1,2,3,4,6,7,8,8a-octahydro-isoquinoline 
• 118646-96-1 (2-cyclohex-1-enyl-ethyl)-(4-methoxy-styryl)-methyl-amine 
• 98237-33-3 1-(4-Methoxybenzyl)-2-methyl-5,6,7,8-tetrahydroisochinoliniumiodide 
• 50-00-0 formaldehyd 
• 51072-36-7 (+)-1-(p-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline 
• 14467-91-5 2-methyl-1,2,3,4,5,6,7,8-octahydroisoquinoline 
• 824-94-2 p-methoxybenzyl chloride 
• 110252-37-4 N-methyl-5,6,7,8-tetrahydroisoquinolinium iodide 
• 5703-26-4 4-Methoxyphenylacetaldehyde 
• 7339-87-9 4-hydroxyphenylacetaldehyde 
• 101871-19-6 (2-cyclohex-1-enyl-ethyl)-methyl-amine 
• 102448-99-7 N-(2-(cyclohex-1-en-1-yl)ethyl)-1,1-diphenylmethanimine 

Downstream Products

• 23667-36-9 6-methyl-2,3,3a,4,5,6,6a,7,11b,11c-decahydro-1H-dibenzo[de,g]quinolin-10-ol 
• 77-07-6 racemorphan 
• 23667-36-9 (+/-)-6-methyl-(3ar,6at,11bt,11ct)-2,3,3a,4,5,6,6a,7,11b,11c-decahydro-1H-dibenzo[de,g]quinolin-10-ol 
• 125-70-2 rac-3-methoxy-17-methyl-morphinane 
• 89614-56-2 (S)-(+)-N-methyl-1-(p-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline 
• 67596-84-3 (+)-2-methyl-1-(4-methoxy)benzyl-1,2,3,4,5,6,7,8-hexahydroisoquinoline 
• 125-70-2 dextromethorphan 
• 66209-45-8 2-cyclobutylcarbonyl-1-(p-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline 
• 51072-36-7 (+)-1-(p-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline 
• 852334-50-0 {2-[2-(4-methoxy-phenethyl)-cyclohexyl]-ethyl}-methyl-amine 
• 95367-72-9 {2-[2-(4-methoxy-phenethyl)-cyclohexyl]-ethyl}-dimethyl-amine 
• 102021-29-4 {2-[2-(4-methoxy-styryl)-cyclohex-1-enyl]-ethyl}-dimethyl-amine 
• 98985-27-4 rac-3-benzyloxy-17-methyl-morphinane 
• 77-07-6 Levorphanol 

Relevant articles and documents

Preparation method of 1-(4-methoxy-benzyl)-2-methyl-octahydro isoquinoline

The invention discloses a preparation method of 1-(4-methoxy-benzyl)-2-methyl-octahydro isoquinoline. The preparation method comprises the following steps: dissolving 1, 2, 3, 4, 5, 6, 7, 8-octahydro-1-(methoxyphenyl) methyl isoquinoline in a solvent, adding a formaldehyde solution, stirring, adding a catalyst, introducing hydrogen, carrying out a catalytic hydrogenation reaction, filtering the catalyst out after the reaction is finished, desolventizing, and carrying out distillation separation to obtain 1-(4-methoxyl-benzyl)-2-methyl-1, 2, 3, 4, 5, 6, 7, 8-octahydro isoquinoline. The method provided by the invention has the characteristics of mild and safe reaction conditions, environmental protection, side reaction reduction, high yield, good purity, simple operation and the like, so that the preparation industry is green, environment-friendly, safe and efficient, and the production cost is reduced.

Selective catalytic hydrogenations and hydrogenolyses, VI: An improved synthesis of 1-benzyl-2-methyloctahydroisoquinolines

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Isoquinolines. I. Preparation and stereochemistry of 9,10 epoxy 1 (p methoxybenzyl) 2 methyldecahydroisoquinolines

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