All Photos(1)
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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Yuxiang Yao et al.
Scientific reports, 3, 3235-3235 (2013-11-19)
5-Hydroxy-2-pyridone (2,5-DHP) is a central metabolic intermediate in catabolism of many pyridine derivatives, and has been suggested as a potential carcinogen. 2,5-DHP is frequently transformed to N-formylmaleamic acid (NFM) by a 2,5-DHP dioxygenase. Three hypotheses were formerly discussed for conversion
Hongzhi Tang et al.
Scientific reports, 2, 377-377 (2012-04-25)
Nicotine is an important chemical compound in nature that has been regarded as an environmental toxicant causing various preventable diseases. Several bacterial species are adapted to decompose this heterocyclic compound, including Pseudomonas and Arthrobacter. Pseudomonas putida S16 is a bacterium
The bacterial oxidation of nicotinic acid.
E J BEHRMAN et al.
The Journal of biological chemistry, 228(2), 923-945 (1957-10-01)
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
Maleamic and citraconamic acids, methyl esters, and imides.
MEHTA NB, et al.
The Journal of Organic Chemistry, 25(6), 1012-1015 (1960)
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