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About This Item
Empirical Formula (Hill Notation):
C5H5NO2
CAS Number:
Molecular Weight:
111.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-226-1
Beilstein/REAXYS Number:
108550
MDL number:
Assay:
97%
Form:
powder
Product Name
N-Methylmaleimide, 97%
InChI key
SEEYREPSKCQBBF-UHFFFAOYSA-N
InChI
1S/C5H5NO2/c1-6-4(7)2-3-5(6)8/h2-3H,1H3
SMILES string
CN1C(=O)C=CC1=O
assay
97%
form
powder
mp
94-96 °C (lit.)
functional group
imide
maleimide
Quality Level
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Application
N-Methylmaleimide can be used:
- In the synthesis of organic structure directing agents for designing silicogermanate zeolites.
- As a dienophile in Diels-Alder reaction.
- For the synthesis of biologically active pyrrolo[2,1-a]isoquinolines.
- As a dipolarophile in [3 + 2] dipolar addition reactions.
- As a co-monomer in atom transfer radical polymerization of styrene to obtain styrene copolymers with programmed microstructure.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Journal of the American Chemical Society, 129(31), 9542-9543 (2007)
The ITQ-37 mesoporous chiral zeolite.
Sun J, et al.
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Visible-light-induced oxidation/[3+ 2] cycloaddition/oxidative aromatization sequence: a photocatalytic strategy to construct pyrrolo [2, 1-a] isoquinolines.
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