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About This Item
Empirical Formula (Hill Notation):
C5H5NO2
CAS Number:
Molecular Weight:
111.10
Beilstein:
108550
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
form
powder
mp
94-96 °C (lit.)
functional group
imide
maleimide
SMILES string
CN1C(=O)C=CC1=O
InChI
1S/C5H5NO2/c1-6-4(7)2-3-5(6)8/h2-3H,1H3
InChI key
SEEYREPSKCQBBF-UHFFFAOYSA-N
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Related Categories
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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