671224-08-1

Basic information

• Product Name: Ethanone, 2-aMino-1-(2,5-diMethoxyphenyl)-, hydrochloride
• Synonyms: Ethanone, 2-aMino-1-(2,5-diMethoxyphenyl)-, hydrochloride;2-Amino-1-(2,5-dimethoxyphenyl)ethanone hydrochloride
• CAS NO: 671224-08-1
• Molecular Formula: C10H13NO3.HCl
• Molecular Weight: 231.67606
• EINECS: -0
• Mol File: 671224-08-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanone, 2-aMino-1-(2,5-diMethoxyphenyl)-, hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-aMino-1-(2,5-diMethoxyphenyl)-, hydrochloride(671224-08-1)
• EPA Substance Registry System: Ethanone, 2-aMino-1-(2,5-diMethoxyphenyl)-, hydrochloride(671224-08-1)

Safety Data

• Hazardous Substances Data: 671224-08-1(Hazardous Substances Data)

Usage

General Description

Ethanone, 2-amino-1-(2,5-dimethoxyphenyl)-, hydrochloride is a chemical compound that belongs to the group of substituted amphetamines. It is a psychoactive drug that acts as a selective serotonin releasing agent and is commonly known by its street name "2C-I". It is known to produce intense visual and auditory hallucinations and has been used recreationally for its psychoactive effects. However, it is also classified as a Schedule I controlled substance in the United States due to its potential for abuse and lack of accepted medical use. It is important to handle and use this chemical with caution and under proper guidance.

Upstream product

• 100-97-0 hexamethylenetetramine 
• 1204-21-3 2-bromo-2',5'-dimethoxyacetophenone 

Relevant articles and documents

Asymmetric hydrogenation of α-primary and secondary amino ketones: Efficient asymmetric syntheses of (-)-arbutamine and (-)-denopamine

Two ss-receptor agonists (-)-denopamine and (-)-arbutamine were prepared in good yields and enantioselectivities by asymmetric hydrogenation of unprotected amino ketones for the first time by using Rh catalysts bearing electron-donating phosphine ligands. A series of α-primary and secondary amino ketones were synthesized and hydrogenated to produce various 1,2-amino alcohols in good yields and with good enantioselectivies. This Rh electron-donating phosphine-catalyzed asymmetric hyderogenation repI resents one of the most promising and convenient approaches towards the asymmetric synthesis of chiral amino alcohols.

AN IMPROVED PROCESS FOR THE SYNTHESIS OF (±) 2-AMINO-N-[2,(S,5-DIMETHOXYPHENYL)-2-HYDROXYETHYL] ACETAMIDE MONOHYDROCHLORIDE

This invention relates to an improved process for synthesizing (±) 2-Amino-N-[2,(S,5-dimethoxyphenyl)-2-hydroxyethyl] acetamide monohydrochloride in good yield and in a cost effective manner from 1-(2,5dimethoxyphenyl)-2-bromoethanone by reacting the same