Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H11NO2 |
| Molecular Weight | 117.1463 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[N+]1([O-])CCOCC1
InChI
InChIKey=LFTLOKWAGJYHHR-UHFFFAOYSA-N
InChI=1S/C5H11NO2/c1-6(7)2-4-8-5-3-6/h2-5H2,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| High substrate specificity and induction characteristics of trimethylamine-N-oxide reductase of Escherichia coli. | 1996 May 2 |
|
| Synthetic studies with 13-deoxybaccatin III. | 2002 Oct 4 |
|
| Synthesis of the minor acrolein adducts of 2(')-deoxyguanosine and their generation in oligomeric DNA. | 2003 Apr |
|
| Wet spinning of Bombyx mori silk fibroin dissolved in N-methyl morpholine N-oxide and properties of regenerated fibres. | 2005 Dec 15 |
|
| Catalytic and biological activities of Ru(III) mixed ligand complexes containing N,O donor of 2-hydroxy-1-naphthylideneimines. | 2005 Jul |
|
| Binuclear ruthenium(III) Schiff base complexes bearing N(4)O(4) donors and their catalytic oxidation of alcohols. | 2008 Dec 1 |
|
| The antimicrobial reagent role on the degradation of model cellulose film. | 2008 Nov 1 |
|
| Synthesis and spectral characterization of 2'-hydroxy chalconate complexes of ruthenium(II) and their catalytic and biological applications. | 2008 Oct |
|
| Nanoscale cellulose films with different crystallinities and mesostructures--their surface properties and interaction with water. | 2009 Jul 7 |
|
| Cellulose nanocrystals/cellulose core-in-shell nanocomposite assemblies. | 2009 Nov 17 |
|
| Studies on the synthesis, spectra, catalytic and antibacterial activities of binuclear ruthenium(II) complexes. | 2010 Sep 15 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
m7441
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | Merck Index | ||
|
ARC64PKJ0F
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
7529-22-8
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
231-391-8
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
82153
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
73198
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
DTXSID3029287
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
N-METHYLMORPHOLINE N-OXIDE
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
52093
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
82029
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY | |||
|
C067960
Created by
admin on Sat Dec 16 20:09:07 GMT 2023 , Edited by admin on Sat Dec 16 20:09:07 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
