165741-71-9

Basic information

• Product Name: N-Methyl-3,4-dimethylbenzylamine
• Synonyms: N-Methyl-3,4-dimethylbenzylamine;1-(3,4-DiMethylphenyl)-N-MethylMethanaMine;N,3,4-Trimethylbenzenemethanamine;1-(3,4-Dimethylphenyl)
• CAS NO: 165741-71-9
• Molecular Formula: C10H15N
• Molecular Weight: 149.2328
• Mol File: 165741-71-9.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: N-Methyl-3,4-dimethylbenzylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Methyl-3,4-dimethylbenzylamine(165741-71-9)
• EPA Substance Registry System: N-Methyl-3,4-dimethylbenzylamine(165741-71-9)

Safety Data

• Hazardous Substances Data: 165741-71-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
N-Methyl-3,4-dimethylbenzylamine is used as a reactant or intermediate in the synthesis of various organic compounds for pharmaceutical and agrochemical applications. Its unique structure allows for the creation of a wide range of products with diverse therapeutic and pesticidal properties.
Used as a Corrosion Inhibitor:
N-Methyl-3,4-dimethylbenzylamine is utilized as a corrosion inhibitor in various industrial applications. Its chemical properties enable it to protect metal surfaces from corrosion, extending the lifespan of equipment and reducing maintenance costs.
Used as a Reagent in Organic Chemistry Reactions:
In the field of organic chemistry, N-Methyl-3,4-dimethylbenzylamine serves as a reagent in various chemical reactions. Its ability to participate in a range of reactions makes it a valuable tool for synthesizing new compounds and conducting research in organic chemistry.
Safety Precautions:
Due to its flammable nature and potential health hazards, including skin and eye irritation, N-Methyl-3,4-dimethylbenzylamine should be handled with care. Proper safety measures, such as wearing protective gear and working in well-ventilated areas, should be taken to minimize risks associated with its use.

InChI:InChI=1S/C10H15N/c1-8-4-5-10(7-11-3)6-9(8)2/h4-6,11H,7H2,1-3H3

Relevant articles and documents

HETEROCYCLIC COMPOUNDS, METHODS OF MAKING THEM AND THEIR USE IN THERAPY

In part, the present invention is directed to antibacterial compounds of formula (I) wherein A is a bicyclic heteroaryl ring or a tricyclic ring and R2 is an heterocyclic residue; L is a bond, or L is alkyl, alkenyl or cycloalkyl.