74572-14-8

Basic information

• Product Name: (S)-2-Ethylmorpholine
• Synonyms: (2S)-2-Ethylmorpholine;(S)-2-Ethylmorpholine;Morpholine, 2-ethyl-, (S)-
• CAS NO: 74572-14-8
• Molecular Formula: C6H13NO
• Molecular Weight: 115.17
• Mol File: 74572-14-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 160.631°C at 760 mmHg
• Flash Point: 54.217°C
• Appearance: /
• Density: 0.878g/cm³
• Vapor Pressure: 2.363mmHg at 25°C
• Refractive Index: 1.414
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (S)-2-Ethylmorpholine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-Ethylmorpholine(74572-14-8)
• EPA Substance Registry System: (S)-2-Ethylmorpholine(74572-14-8)

Safety Data

• Hazardous Substances Data: 74572-14-8(Hazardous Substances Data)

Usage

General Description

"(S)-2-Ethylmorpholine" is a chemical compound that belongs to the family of morpholine derivatives. It is an organic compound with the molecular formula C6H13NO, and it has a chiral center which gives rise to its (S)-stereoisomer. This chemical is a colorless to yellowish liquid with a slightly amine-like odor. (S)-2-Ethylmorpholine is commonly used as a solvent in various chemical reactions and processes, and it also finds application as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique chemical properties and reactivity make it a valuable compound in the field of organic synthesis and industrial applications.

InChI:InChI=1/C6H13NO/c1-2-6-5-7-3-4-8-6/h6-7H,2-5H2,1H3/t6-/m0/s1

Upstream product

• 74572-08-0 (S)-1-(2-Hydroxy-ethylamino)-butan-2-ol 
• 74572-11-5 (S)-2-Ethyl-4-(toluene-4-sulfonyl)-morpholine 

Relevant articles and documents

SYNTHESIS AND ABSOLUTE CONFIGURATION OF SUBSTITUTED MORPHOLINES

We studied methods of stereospecific synthesis that enabled us to obtain variously substituted morpholinic compounds and to determine their absolute configuration.From a study of the chiroptical properties of synthetic N-(2-pyridyl-N-oxide) derivatives of optically active morpholines, it was possible to correlate the sign of the Cotton effect with the absolute configuration.This correlation agrees with that previously established for derivatives of the piperidine type.By evaluating the various contributions to the Cotton effect of substituents in positions 2 and 3, we established the absolute configuration of bicyclic compounds condensed in the two positions mentioned above.