Weight | 97.073 g/mol |
---|---|
Formula | C4H3NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
MALEIMIDE (541-59-3)
maleimide, potassium, silver (+1) (2:1:1) salt · maleimide, silver (+1) salt
Score:
#1857 in Physics
,
#2272 in Biochemistry
,
#5781 in Chemistry
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- Maleimide-functionalized self-assembled monolayers for the preparation of peptide and carbohydrate biochips (Langmuir, 2003)
- The furan/maleimide DielsAlder reaction: A versatile clickunclick tool in macromolecular synthesis (Progress in Polymer Science, 2013)
- More useful maleimide compounds for the conjugation of Fab' to horseradish peroxidase through thiol groups in the hinge. (Biotechnology and Applied Biochemistry, 1984)
- AnthraceneMaleimide-Based DielsAlder Click Chemistry as a Novel Route to Graft Copolymers (Macromolecules, 2006)
- Analysis of glutathione, glutathione disulfide, cysteine, homocysteine, and other biological thiols by high-performance liquid chromatography following derivatization by n-(1-pyrenyl)maleimide. (Analytical Biochemistry, 1995)
- Maleimide CrossLinked Bioactive PEG Hydrogel Exhibits Improved Reaction Kinetics and CrossLinking for Cell Encapsulation and In Situ Delivery (Advanced Materials, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - maleimide, potassium, silver (+1) (2:1:1) salt
- maleimide, silver (+1) salt
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SMILESC1=CC(=O)NC1=O
-
InChIKeyPEEHTFAAVSWFBL-UHFFFAOYSA-N
- Pubchem - MALEIMIDE
- Wikipedia - maleimide
Maleimide is a chemical compound with the formula H2C2(CO)2NH (see diagram). This unsaturated imide is an important building block in organic synthesis. The name is a contraction of maleic acid and imide, the -C(O)NHC(O)- functional group.
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