CAS 29753-26-2: N-(4-Aminophenyl)maleimide
Formula:C10H8N2O2
InChI:InChI=1S/C10H8N2O2/c11-7-1-3-8(4-2-7)12-9(13)5-6-10(12)14/h1-6H,11H2
InChI key:InChIKey=XOPCHXSYQHXLHJ-UHFFFAOYSA-N
SMILES:O=C1N(C(=O)C=C1)C2=CC=C(N)C=C2
Synonyms:- (p-Aminophenyl)maleimide
- 1-(4-Aminophenyl)-1H-pyrrole-2,5-dione
- 1-(4-Aminophenyl)-2,5-dihydro-1H-pyrrole-2,5-dione
- 1-(4-Aminophenyl)pyrrole-2,5-dione
- 1H-Pyrrole-2,5-dione, 1-(4-aminophenyl)-
- N-(p-Aminophenyl)maleimide
- N-(4-Aminophenyl)maleimide
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Found 5 products.
N-(4-Aminophenyl)malemide
CAS:N-(4-Aminophenyl)malemideFormula:C10H8N2O2Purity:By hplc: 97.3% by area (210nm) (Typical Value in Batch COA)Color and Shape: orange/tan powderMolecular weight:188.18g/molN-(4-Aminophenyl)maleimide
CAS:Formula:C10H8N2O2Purity:>93.0%(T)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:188.19N-(4-Aminophenyl)maleimide
CAS:N-(4-Aminophenyl)maleimide is a bifunctional chemical that reacts with the sulfhydryl groups in proteins. It is used as a model system to study the mechanism of action of alkylating agents and their effect on biological systems. N-(4-Aminophenyl)maleimide reacts with disulphides and paraformaldehyde, which are commonly found in tissues, to form fluorescent endpoints. This reaction can be detected by staining sections of tissue with diaminobenzidine and examining under ultraviolet light or by using an electron microscope. The organomercurials methyl mercury chloride and dimethyl mercury chloride can be reduced catalytically by N-(4-aminophenyl)maleimide to form the corresponding mercaptides. Chemical analyses have shown that this reaction is reversible, forming N-(4-aminophenyl)maleimide as a product.Formula:C10H8N2O2Purity:Min. 95%Molecular weight:188.19 g/mol1H-Pyrrole-2,5-dione, 1-(4-aminophenyl)-
CAS:Formula:C10H8N2O2Purity:93%Color and Shape:SolidMolecular weight:188.18271-(4-Aminophenyl)-1H-pyrrole-2,5-dione
CAS:Purity:93%Color and Shape:SolidMolecular weight:188.18600463867188
