64334-96-9

Basic information

• Product Name: 7-Quinolinamine,2-methyl-(9CI)
• Synonyms: 7-Quinolinamine,2-methyl-(9CI)
• CAS NO: 64334-96-9
• Molecular Formula: C₁₀H₁₀N₂
• Molecular Weight: 158.1998
• Product Categories: ISOQUINOLINE
• Mol File: 64334-96-9.mol
• Article Data: 9

Chemical Properties

• Melting Point: 148°C
• Boiling Point: 333.29°C (estimate)
• Appearance: /
• Density: 1.1606 (estimate)
• Refractive Index: 1.7080 (estimate)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 7-Quinolinamine,2-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Quinolinamine,2-methyl-(9CI)(64334-96-9)
• EPA Substance Registry System: 7-Quinolinamine,2-methyl-(9CI)(64334-96-9)

Safety Data

• Hazardous Substances Data: 64334-96-9(Hazardous Substances Data)

Usage

General Description

7-Quinolinamine,2-methyl-(9CI) is a chemical compound with a variety of potential applications. It belongs to the class of organic compounds known as quinolines and derivatives, which are compounds containing a quinoline moiety, a structure made up of a benzene ring fused to a pyridine ring. The structure of 7-Quinolinamine,2-methyl-(9CI) consists of a methyl group substituted onto the 2-position of a quinolinamine backbone. Due to its structure, it could potentially be used in research activities or industrial applications, such as pharmaceutical drug manufacturing. However, there is limited information available about its specific uses, safety, and toxicological properties.

Upstream product

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Relevant articles and documents

HETEROCYCLIC CARBOXYLIC ACID AMIDE LIGAND AND APPLICATIONS THEREOF IN COPPER CATALYZED COUPLING REACTION OF ARYL HALOGENO SUBSTITUTE

Provided are a heterocyclic carboxylic acid amide ligand and applications thereof in a copper catalyzed coupling reaction. Specifically, provided are uses of a compound represented by formula (I), definitions of radical groups being described in the specifications. The compound represented by formula (I) can be used as the ligand in the copper catalyzed coupling reaction of the aryl halogeno substitute, and is used or catalyzing the coupling reaction for forming the aryl halogeno substitute having C—N, C—O, C—S and other bonds.

Discovery of N-(Naphthalen-1-yl)-N′-alkyl Oxalamide Ligands Enables Cu-Catalyzed Aryl Amination with High Turnovers

A class of N-(naphthalen-1-yl)-N′-alkyl oxalamides have been proven to be powerful ligands, making a coupling reaction of (hetero)aryl iodides with primary amines proceed at 50 °C with only 0.01 mol % of Cu2O and ligand as well as a coupling reaction of (hetero)aryl bromides with primary amines and ammonia at 80 °C with only 0.1 mol % of Cu2O and ligand. A wide range of coupling partners work well under these conditions, thereby providing an easy to operate method for preparing (hetero)aryl amines.

Assembly of Primary (Hetero)Arylamines via CuI/Oxalic Diamide-Catalyzed Coupling of Aryl Chlorides and Ammonia

A general and practical catalytic system for aryl amination of aryl chlorides with aqueous or gaseous ammonia has been developed, with CuI as the catalyst and bisaryl oxalic diamides as the ligands. The reaction proceeds at 105-120°C to provide a diverse set of primary (hetero)aryl amines in high yields with various functional groups.