1304771-27-4

Basic information

• Product Name: (S)-1-(3-Methoxyphenyl)ethanamine hydrochloride
• Synonyms: (S)-1-(3-Methoxyphenyl)ethanamine hydrochloride;S-3-methoxy-α-methylbenzylamine hydrochloride
• CAS NO: 1304771-27-4
• Molecular Formula: C₉H₁₃NO*ClH
• Molecular Weight: 187.66656
• Mol File: 1304771-27-4.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (S)-1-(3-Methoxyphenyl)ethanamine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(3-Methoxyphenyl)ethanamine hydrochloride(1304771-27-4)
• EPA Substance Registry System: (S)-1-(3-Methoxyphenyl)ethanamine hydrochloride(1304771-27-4)

Safety Data

• Hazardous Substances Data: 1304771-27-4(Hazardous Substances Data)

Usage

General Description

(S)-1-(3-Methoxyphenyl)ethanamine hydrochloride is a chemical compound with the molecular formula C9H14NO.ClH. It is a hydrochloride salt of (S)-1-(3-Methoxyphenyl)ethanamine, which is a chiral amine. (S)-1-(3-Methoxyphenyl)ethanamine hydrochloride is commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds due to its ability to introduce a chiral amine functionality into the molecule. It is also used as a building block in the synthesis of biologically active compounds and pharmaceutical intermediates. Additionally, this compound has potential applications in research and development, particularly in the field of medicinal chemistry.

Upstream product

• 50919-07-8 (S)-1-(3-methoxyphenyl)ethylamine 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 1164111-45-8 C₉H₁₁NO*ClH 

Relevant articles and documents

Donor Amine Salt-Based Continuous in situ-Product Crystallization in Amine Transaminase-Catalyzed Reactions

The unfavorable reaction equilibrium of transaminase-catalyzed reactions is a major challenge for the efficient biocatalytic synthesis of chiral amines. In this study the synthetic utilization of a salt-based, continuous in situ-product crystallization is

Development of an in situ-Product Crystallization (ISPC)-Concept to Shift the Reaction Equilibria of Selected Amine Transaminase-Catalyzed Reactions

The synthesis of enantiopure amines via amine transaminases involves several challenges including unfavorable reaction equilibria and product inhibition. Described here is a non-catalytic approach to overcome such problems by using an in situ-product crystallization (ISPC) to selectively remove a targeted product amine from an amine transaminase-catalyzed reaction. The continuous removal of the product amine from its reaction solution as a barely soluble salt effectively yields a displacement of the reaction equilibrium towards the products and facilitates a simple downstream processing approach via filtration. The targeted product amine is eventually obtained from the salt, while the counterion compound can be easily recycled.