Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:132844 - glycidyl methacrylate
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
glycidyl methacrylate
ChEBI ID
CHEBI:132844
Definition
An enoate ester obtained by formal condensation of the carboxy group of methacrylic acid with the hydroxy group of glycidol.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
qingping liu
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Wikipedia
License
Read full article at Wikipedia
Formula
C7H10O3
Net Charge
0
Average Mass
142.153
Monoisotopic Mass
142.06299
InChI
InChI=1S/C7H10O3/c1-5(2)7(8)10-4-6-3-9-6/h6H,1,3-4H2,2H3
InChIKey
VOZRXNHHFUQHIL-UHFFFAOYSA-N
SMILES
O1C(C1)COC(=O)C(C)=C
ChEBI Ontology
Outgoing
glycidyl methacrylate (
CHEBI:132844
)
has functional parent
glycidol (
CHEBI:30966
)
glycidyl methacrylate (
CHEBI:132844
)
has functional parent
methacrylic acid (
CHEBI:25219
)
glycidyl methacrylate (
CHEBI:132844
)
is a
enoate ester (
CHEBI:51702
)
glycidyl methacrylate (
CHEBI:132844
)
is a
epoxide (
CHEBI:32955
)
IUPAC Name
(oxiran-2-yl)methyl 2-methylprop-2-enoate
Synonyms
Sources
2,3-Epoxypropanol methacrylate
NIST Chemistry WebBook
2,3-Epoxypropyl methacrylate
ChemIDplus
2-((Methacryloxy)methyl)oxirane
ChemIDplus
Glycidol methacrylate
ChemIDplus
Glycidyl α-methylacrylate
NIST Chemistry WebBook
Glycidyl alpha-methylacrylate
ChemIDplus
Methacrylic acid, 2,3-epoxypropyl ester
ChemIDplus
Manual Xref
Database
Glycidyl_methacrylate
Wikipedia
View more database links
Registry Numbers
Types
Sources
106-91-2
CAS Registry Number
NIST Chemistry WebBook
106-91-2
CAS Registry Number
ChemIDplus
2506
Reaxys Registry Number
Reaxys
Citation
Type
Source
27394038
PubMed citation
Europe PMC
Last Modified
27 January 2017