Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H9NO3 |
| Molecular Weight | 155.1513 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=C)C(=O)OCCN=C=O
InChI
InChIKey=RBQRWNWVPQDTJJ-UHFFFAOYSA-N
InChI=1S/C7H9NO3/c1-6(2)7(10)11-4-3-8-5-9/h1,3-4H2,2H3
| Molecular Formula | C7H9NO3 |
| Molecular Weight | 155.1513 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of poly(methyl urethane) acrylate oligomer using 2-isocyanatoethyl methacrylate for UV curable coating. | 2009-02 |
|
| Photocrosslinkable starch-based polymers for ophthalmologic drug delivery. | 2008-11-01 |
|
| Controlled cyclopolymerization through quantitative 19-membered ring formation. | 2008-08-20 |
|
| Development of a new photocrosslinkable biodegradable bioadhesive. | 2008-03-20 |
|
| Synthesis and preparation of novel 4-arm star-shape poly(carboxylic acid)s for improved light-cured glass-ionomer cements. | 2007-04 |
|
| Influence of peripheral hydrogen bonding on the mechanical properties of photo-cross-linked star-shaped poly(D,L-lactide) networks. | 2005-09-13 |
|
| Synthesis and characterization of PEG dimethacrylates and their hydrogels. | 2004-07-13 |
|
| Nano-scaled hydroxyapatite/polymer composite I. Coating of sintered hydroxyapatite particles on poly(gamma-methacryloxypropyl trimethoxysilane)grafted silk fibroin fibers through chemical bonding. | 2004-01 |
|
| Preparation of nanoparticles composed with bioinspired 2-methacryloyloxyethyl phosphorylcholine polymer. | 2001-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:10:44 GMT 2025
by
admin
on
Mon Mar 31 22:10:44 GMT 2025
|
| Record UNII |
828DBI7X91
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
35409
Created by
admin on Mon Mar 31 22:10:44 GMT 2025 , Edited by admin on Mon Mar 31 22:10:44 GMT 2025
|
PRIMARY | |||
|
30674-80-7
Created by
admin on Mon Mar 31 22:10:44 GMT 2025 , Edited by admin on Mon Mar 31 22:10:44 GMT 2025
|
PRIMARY | |||
|
250-284-7
Created by
admin on Mon Mar 31 22:10:44 GMT 2025 , Edited by admin on Mon Mar 31 22:10:44 GMT 2025
|
PRIMARY | |||
|
6350
Created by
admin on Mon Mar 31 22:10:44 GMT 2025 , Edited by admin on Mon Mar 31 22:10:44 GMT 2025
|
PRIMARY | |||
|
DTXSID6051986
Created by
admin on Mon Mar 31 22:10:44 GMT 2025 , Edited by admin on Mon Mar 31 22:10:44 GMT 2025
|
PRIMARY | |||
|
828DBI7X91
Created by
admin on Mon Mar 31 22:10:44 GMT 2025 , Edited by admin on Mon Mar 31 22:10:44 GMT 2025
|
PRIMARY | |||
|
Methacryloyloxyethyl isocyanate
Created by
admin on Mon Mar 31 22:10:44 GMT 2025 , Edited by admin on Mon Mar 31 22:10:44 GMT 2025
|
PRIMARY |