76143-84-5

Basic information

• Product Name: Isoquinoline, 7-methoxy-1-methyl-
• CAS NO: 76143-84-5
• Molecular Formula: C11H11NO
• Mol File: 76143-84-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Isoquinoline, 7-methoxy-1-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoquinoline, 7-methoxy-1-methyl-(76143-84-5)
• EPA Substance Registry System: Isoquinoline, 7-methoxy-1-methyl-(76143-84-5)

Safety Data

• Hazardous Substances Data: 76143-84-5(Hazardous Substances Data)

Usage

General Description

Isoquinoline, 7-methoxy-1-methyl- is a chemical compound with the molecular formula C11H11NO that belongs to the class of heterocyclic compounds, specifically an isoquinoline with a methoxy substituent at the 7-position and a methyl group at the 1-position. It is a pale yellow solid that is commonly used in the synthesis of pharmaceuticals and as a precursor in the production of other chemicals. Isoquinoline, 7-methoxy-1-methyl- has also been studied for its potential medicinal properties, including its reported anti-inflammatory and anticonvulsant effects. However, further research is required to fully understand its pharmacological properties and potential applications.

Upstream product

• 39989-39-4 7-methoxyisoquinoline 
• 67-68-5 dimethyl sulfoxide 
• 76143-78-7 [1-(3-methoxy-phenyl)-ethylamino]-acetaldehyde diethylacetal 
• 51673-84-8 dimethoxyacetaldehyde 
• 854184-18-2 (+/-)-1-(3-methoxyphenyl)ethylamine hydrochloride 
• 122806-25-1 1-(3-methoxy-phenyl)-ethanone oxime 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 108-05-4 vinyl acetate 
• 1257846-26-6 (E)-1-(3-methoxyphenyl) ethanone O-acetyl oxime 
• 61190-04-3 (2,2-Diethoxy-ethyl)-[1-(3-methoxy-phenyl)-meth-(Z)-ylidene]-amine 

Downstream Products

• 81593-62-6 7-methoxy-1-methyl-2-<4-(3,4-dimethoxybenzoyloxy)butyl>isoquinolinium iodide 
• 140683-34-7 7-Methylamino-1-methylisoquinoline 
• 31181-23-4 1-methyl-7-hydroxyisoquinoline 
• 81593-51-3 1,2,3,4-tetrahydro-7-methoxy-1-methyl-2-<4-(3,4-dimethoxybenzoyloxy)butyl>isoquinoline hydrochloride 

Relevant articles and documents

Synthesis and SAR Studies of Isoquinoline and Tetrahydroisoquinoline Derivatives as Melatonin Receptor Ligands

In our constant search for new successors of agomelatine, we report herein a new series of compounds resulting from bioisosteric modulation of the naphthalene ring. The isoquinoline and tetrahydroisoquinoline derivatives were synthesized and pharmacologic

Reaction of isoquinoline 2-oxides with methylsulfinylmethyl carbanion

7-Methoxy-3-methylsulfonyl-3H-benz[d]azepine (5) and 2-deuterio-3-(methyl-d3)-sulfonyl-3H-benz[d]azepine (14) were obtained from the reaction of the corresponding isoquinoline 2-oxides with methylsulfinylmethyl carbanion. A revised reaction mechanism is proposed on the basis of the results obtained by use of deuterated dimethyl sulfoxide-d6.

Spasmolytic agents. I. Aminoalcohol esters having a phenethylamine-like moiety

-