112767-81-4

Basic information

• Product Name: (2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride
• Synonyms: (R)-2-(((3,4-Dimethoxyphenyl)methyl)amino)-1-butanol hydrochloride; 1-Butanol, 2-(((3,4-dimethoxyphenyl)methyl)amino)-, hydrochloride, (R)-
• CAS NO: 112767-81-4
• Molecular Formula: C₁₃H₂₂ClNO₃
• Molecular Weight: 275.7717
• Mol File: 112767-81-4.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 375.1°C at 760 mmHg
• Flash Point: 180.7°C
• Vapor Pressure: 2.71E-06mmHg at 25°C
• CAS DataBase Reference: (2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: (2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride(112767-81-4)
• EPA Substance Registry System: (2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride(112767-81-4)

Safety Data

• Hazardous Substances Data: 112767-81-4(Hazardous Substances Data)

Usage

Description

(2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride is a chiral amine and quaternary ammonium salt compound characterized by its unique (2R) configuration. It consists of a hydroxybutan-2-aminium cation paired with a chloride anion, and features a 3,4-dimethoxybenzyl group that endows it with distinct chemical properties and potential biological activities. (2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride holds promise for applications in medicinal chemistry and drug development due to its structural features and pharmacological potential.

Uses

Used in Medicinal Chemistry:
(2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride is utilized as a building block or intermediate in the synthesis of pharmaceuticals, leveraging its unique structural elements and chiral properties to create novel therapeutic agents.
Used in Drug Development:
In the pharmaceutical industry, (2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride serves as a candidate for drug development, potentially leading to the discovery of new medications with improved efficacy and selectivity due to its specific configuration and functional groups.
Used in Chiral Synthesis:
(2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride is employed as a chiral source in asymmetric synthesis, contributing to the production of enantiomerically pure compounds that are essential in various biological and medicinal applications.
Used in Research:
In academic and research settings, (2R)-N-(3,4-dimethoxybenzyl)-1-hydroxybutan-2-aminium chloride is used as a subject of study to explore its chemical reactivity, potential interactions with biological targets, and its role in understanding the stereochemistry of biochemical processes.