1344921-45-4

Basic information

• Product Name: (S)-1-[4-(morpholin-4-yl)phenyl]ethanol
• Synonyms: (S)-1-[4-(morpholin-4-yl)phenyl]ethanol
• CAS NO: 1344921-45-4
• Molecular Weight: 207.272
• Mol File: 1344921-45-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-1-[4-(morpholin-4-yl)phenyl]ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-[4-(morpholin-4-yl)phenyl]ethanol(1344921-45-4)
• EPA Substance Registry System: (S)-1-[4-(morpholin-4-yl)phenyl]ethanol(1344921-45-4)

Safety Data

• Hazardous Substances Data: 1344921-45-4(Hazardous Substances Data)

Usage

General Description

(S)-1-[4-(morpholin-4-yl)phenyl]ethanol, also known as morpholinephenylethanol, is a chemical compound with the molecular formula C13H17NO2. It is a chiral alcohol with a 4-morpholinephenyl moiety attached to the carbon atom. (S)-1-[4-(morpholin-4-yl)phenyl]ethanol is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its chiral nature and potential biological activity. It may also have applications in the development of new materials and as a building block for various organic reactions. As a versatile compound, (S)-1-[4-(morpholin-4-yl)phenyl]ethanol has potential uses in a variety of industries and research fields.

Upstream product

• 115833-91-5 1-(4-(4-morpholinylphenyl))ethan-1-ol 
• 403-42-9 1-(4-fluorophenyl)ethanone 
• 39910-98-0 4-morpholinoacetophenone 

Relevant articles and documents

Visible-Light-Driven Catalytic Deracemization of Secondary Alcohols

Deracemization of racemic chiral compounds is an attractive approach in asymmetric synthesis, but its development has been hindered by energetic and kinetic challenges. Here we describe a catalytic deracemization method for secondary benzylic alcohols which are important synthetic intermediates and end products for many industries. Driven by visible light only, this method is based on sequential photochemical dehydrogenation followed by enantioselective thermal hydrogenation. The combination of a heterogeneous dehydrogenation photocatalyst and a chiral molecular hydrogenation catalyst is essential to ensure two distinct pathways for the forward and reverse reactions. These reactions convert a large number of racemic aryl alkyl alcohols into their enantiomerically enriched forms in good yields and enantioselectivities.

Iron- and cobalt-catalyzed asymmetric hydrosilylation of ketones and enones with bis(oxazolinylphenyl)amine ligands

Chiral bis(oxazolinylphenyl)amines proved to be efficient auxiliary ligands for iron and cobalt catalysts with high activity for asymmetric hydrosilylation of ketones and asymmetric conjugate hydrosilylation of enones.