65771-94-0

Basic information

• Product Name: 1-[2-(3,4-dimethoxyphenyl)ethyl]-3-(methoxycarbonyl)pyridinium
• CAS NO: 65771-94-0
• Molecular Formula: C₁₇H₂₀NO₄
• Molecular Weight: 302.3445
• Mol File: 65771-94-0.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: 1-[2-(3,4-dimethoxyphenyl)ethyl]-3-(methoxycarbonyl)pyridinium(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-(3,4-dimethoxyphenyl)ethyl]-3-(methoxycarbonyl)pyridinium(65771-94-0)
• EPA Substance Registry System: 1-[2-(3,4-dimethoxyphenyl)ethyl]-3-(methoxycarbonyl)pyridinium(65771-94-0)

Safety Data

• Hazardous Substances Data: 65771-94-0(Hazardous Substances Data)

Usage

Chemical family

Pyridinium family This compound belongs to a group of nitrogen-containing, aromatic heterocyclic compounds.

Cationic molecule

Positively charged The compound has a net positive charge due to the presence of the pyridinium ring.

Pyridinium ring structure

Six-membered nitrogen-containing ring The core structure of the compound, which contributes to its unique chemical properties and reactivity.

Substituents

3,4-dimethoxyphenylethyl group and methoxycarbonyl group These functional groups are attached to the pyridinium ring, influencing the compound's reactivity and properties.

3,4-dimethoxyphenylethyl group

Electron-donating and steric effects This group provides additional electron density and steric hindrance, affecting the compound's reactivity and interactions with other molecules.

Methoxycarbonyl group

Electron-withdrawing and ester functionality This group increases the electron-withdrawing ability of the molecule and introduces ester reactivity, allowing for further chemical modifications.

Organic chemistry application

Reactant or intermediate in synthesis reactions The compound is used as a building block or a stepping stone in the synthesis of more complex organic molecules.

Biological activity

Exhibits activity in certain contexts The compound may have potential applications in the field of biology, such as drug development or studying biological processes.

Unique chemical properties

Influenced by the pyridinium group The presence of the pyridinium ring gives the compound distinct chemical characteristics, making it valuable for various research and industrial applications.