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Details

Stereochemistry ACHIRAL
Molecular Formula C7H11NO2
Molecular Weight 141.1677
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Acryloyl Morpholine

SMILES

C=CC(=O)N1CCOCC1

InChI

InChIKey=XLPJNCYCZORXHG-UHFFFAOYSA-N
InChI=1S/C7H11NO2/c1-2-7(9)8-3-5-10-6-4-8/h2H,1,3-6H2

HIDE SMILES / InChI

Molecular Formula C7H11NO2
Molecular Weight 141.1677
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Hydrophilic monomers suppress the adsorption of plasma protein onto a poly(vinylidene fluoride) membrane.
2011-04-09
Evasion of the accelerated blood clearance phenomenon by coating of nanoparticles with various hydrophilic polymers.
2010-10-11
Micelles for delivery of nitric oxide.
2009-10-14
Enhanced antiviral activity of Acyclovir loaded into beta-cyclodextrin-poly(4-acryloylmorpholine) conjugate nanoparticles.
2009-07-20
Preparation and applications of a variety of fluoroalkyl end-capped oligomer/hydroxyapatite composites.
2008-04-15
Cobalt-catalyzed reductive Mannich reactions of 4-acryloylmorpholine with N-tosyl aldimines.
2008-01-07
Synthesis and performance of amphiphilic copolymers for blood cell separation.
2006-08
Incorporation of substituted acrylamides to the lamellar mesophase of Aerosol OT.
2006-07-01
Antitumor polycyclic acridines. 17. Synthesis and pharmaceutical profiles of pentacyclic acridinium salts designed to destabilize telomeric integrity.
2005-11-17
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:05:54 GMT 2025
Edited
by admin
on Mon Mar 31 21:05:54 GMT 2025
Record UNII
K0Y58P61JA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-(MORPHOLIN-4-YL)PROP-2-EN-1-ONE
Preferred Name English
Acryloyl Morpholine
INCI  
Official Name English
2-PROPEN-1-ONE, 1-(4-MORPHOLINYL)-
Systematic Name English
NSC-162221
Code English
Code System Code Type Description
PUBCHEM
98723
Created by admin on Mon Mar 31 21:05:54 GMT 2025 , Edited by admin on Mon Mar 31 21:05:54 GMT 2025
PRIMARY
NSC
162221
Created by admin on Mon Mar 31 21:05:54 GMT 2025 , Edited by admin on Mon Mar 31 21:05:54 GMT 2025
PRIMARY
CAS
5117-12-4
Created by admin on Mon Mar 31 21:05:54 GMT 2025 , Edited by admin on Mon Mar 31 21:05:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID0044947
Created by admin on Mon Mar 31 21:05:54 GMT 2025 , Edited by admin on Mon Mar 31 21:05:54 GMT 2025
PRIMARY
FDA UNII
K0Y58P61JA
Created by admin on Mon Mar 31 21:05:54 GMT 2025 , Edited by admin on Mon Mar 31 21:05:54 GMT 2025
PRIMARY