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About This Item
Linear Formula:
H2NCOCH=CHCO2H
CAS Number:
Molecular Weight:
115.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
form
solid
Quality Level
mp
158-161 °C (lit.)
functional group
amide
carboxylic acid
SMILES string
[H]\C(=C(/[H])C(O)=O)C(N)=O
InChI
1S/C4H5NO3/c5-3(6)1-2-4(7)8/h1-2H,(H2,5,6)(H,7,8)/b2-1-
InChI key
FSQQTNAZHBEJLS-UPHRSURJSA-N
Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
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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Maleamic and citraconamic acids, methyl esters, and imides.
MEHTA NB, et al.
The Journal of Organic Chemistry, 25(6), 1012-1015 (1960)
Juan Rodrigues et al.
Pharmaceutical research, 28(4), 907-919 (2010-12-25)
The objective of this study was to investigate the effect of new 4-maleamic acid and 4-maleamide peptidyl chalcone derivatives against human prostate cancer in vitro and in vivo. From a series of 21 chalcones, the effects of the three best
Meifang Huang et al.
International journal of biological macromolecules, 36(1-2), 98-102 (2005-06-14)
N-maleamic acid-chitosan was synthesized and characterized by Fourier transform infrared spectra analysis (FT-IR) and 1H NMR. The graft copolymerization of N-maleamic acid-chitosan and butyl acrylate (BA) in acetic acid aqueous solution was investigated, using the gamma-ray of 60Co gamma-irradiation method.
Shengzu Zhang et al.
Journal of separation science, 31(21), 3782-3787 (2008-10-18)
The polymerizable gelator N-octadecyl maleamic acid (ODMA) can self-assemble in selected polymerizable organic solvents, such as 2-hydroxyethyl methacrylate (HEMA) and methylacrylic acid (MAA) to form thermally stable polymerizable organogels. A mixture consisting of HEMA and MAA as the monomer and
José I Jiménez et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(32), 11329-11334 (2008-08-06)
The aerobic catabolism of nicotinic acid (NA) is considered a model system for degradation of N-heterocyclic aromatic compounds, some of which are major environmental pollutants; however, the complete set of genes as well as the structural-functional relationships of most of
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