1332832-15-1

Basic information

• Product Name: (S)-1-(2-Methoxyphenyl)ethanamine hydrochloride
• Synonyms: (1S)-1-(2-methoxyphenyl)ethanamine,hydrochloride;(S)-1-(2-METHOXYPHENYL)ETHANAMINE HYDROCHLRIDE
• CAS NO: 1332832-15-1
• Molecular Formula: C₉H₁₃NO*ClH
• Molecular Weight: 187.66656
• Mol File: 1332832-15-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: (S)-1-(2-Methoxyphenyl)ethanamine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(2-Methoxyphenyl)ethanamine hydrochloride(1332832-15-1)
• EPA Substance Registry System: (S)-1-(2-Methoxyphenyl)ethanamine hydrochloride(1332832-15-1)

Safety Data

• Hazardous Substances Data: 1332832-15-1(Hazardous Substances Data)

Usage

General Description

(S)-1-(2-Methoxyphenyl)ethanamine hydrochloride is a chemical compound that is also known as 1-(o-Methoxyphenyl)-1-ethanamine hydrochloride. It is a chiral amine with a structure similar to amphetamine and can act as a central nervous system stimulant. It is commonly used in research and pharmaceutical applications, such as in the development of new medications for conditions such as depression and attention deficit hyperactivity disorder (ADHD). (S)-1-(2-Methoxyphenyl)ethanamine hydrochloride is often sought after due to its potential therapeutic effects, and its use is strictly regulated due to its psychoactive properties.

Upstream product

• 1164111-48-1 C₉H₁₁NO*ClH 
• 40023-74-3 (S)-1-(2-methoxyphenyl)ethanamine 
• 17087-50-2 (+/-)-2-methoxy-α-methylbenzylamine hydrochloride 

Downstream Products

• 40023-74-3 (S)-1-(2-methoxyphenyl)ethanamine 
• 1332828-02-0 (S)-[1-(2-methoxy-phenyl)-ethyl]pyridin-2-ylmethylamine 
• 1332827-97-0 (S)-2,2,2-trifluoro-N-(1-(2-methoxyphenyl)ethyl)acetamide 

Relevant articles and documents

Rhodium-catalyzed asymmetric hydrogenation of unprotected NH imines assisted by a thiourea

Asymmetric hydrogenation of unprotected NH imines catalyzed by rhodium/bis(phosphine)-thiourea provided chiral amines with up to 97% yield and 95% ee. 1HNMR studies, coupled with control experiments, implied that catalytic chloride-bound intermediates were involved in the mechanism through a dual hydrogen-bonding interaction. Deuteration experiments proved that the hydrogenation proceeded through a pathway consistent with an imine.

COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS

The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.