19319-30-3

Basic information

• Product Name: N-hydroxy-4-[(E)-3-hydroxy-3-keto-2-phenyl-prop-1-enyl]benzeneamine oxide
• Synonyms: (2E)-3-(4-nitrophenyl)-2-phenylacrylic acid;(E)-3-(4-nitrophenyl)-2-phenyl-acrylic acid;(E)-3-(4-nitrophenyl)-2-phenyl-prop-2-enoic acid;(E)-3-(4-nitrophenyl)-2-phenylprop-2-enoic acid;N-hydroxy-4-[(E)-3-hydroxy-3-keto-2-phenyl-prop-1-enyl]benzeneamine oxide;N-hydroxy-4-[(E)-3-hydroxy-3-oxo-2-phenyl-prop-1-enyl]benzeneamine oxide;N-hydroxy-4-[(E)-3-hydroxy-3-oxo-2-phenylprop-1-enyl]benzeneamine oxide;3-(4-Nitro-phenyl)-2-phenyl-acrylic acid
• CAS NO: 19319-30-3
• Molecular Formula: C₁₅H₁₁NO₄
• Molecular Weight: 269.26
• Mol File: 19319-30-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-hydroxy-4-[(E)-3-hydroxy-3-keto-2-phenyl-prop-1-enyl]benzeneamine oxide(CAS DataBase Reference)
• NIST Chemistry Reference: N-hydroxy-4-[(E)-3-hydroxy-3-keto-2-phenyl-prop-1-enyl]benzeneamine oxide(19319-30-3)
• EPA Substance Registry System: N-hydroxy-4-[(E)-3-hydroxy-3-keto-2-phenyl-prop-1-enyl]benzeneamine oxide(19319-30-3)

Safety Data

• Hazardous Substances Data: 19319-30-3(Hazardous Substances Data)

Upstream product

• 103-82-2 phenylacetic acid 
• 555-16-8 4-nitrobenzaldehdye 
• 114-70-5 sodium phenylacetate 
• 2929-91-1 4-nitrobenzylidene diacetate 

Downstream Products

• 6624-53-9 (Z)-1-nitro-4-(2-phenylethenyl)-benzene 
• 6318-46-3 2-phenyl-3-(4-aminophenyl)propionic acid 
• 42443-21-0 methyl (E)-3-(4-nitrophenyl)-2-phenylacrylate 
• 52873-63-9 (2E)-3-(4-aminophenyl)-2-phenylprop-2-enoic acid 
• 83743-97-9 3t-(4-nitro-phenyl)-2-phenyl-acryloyl chloride 
• 52873-64-0 (2Z)-3-(4-aminophenyl)-2-phenylprop-2-enoic acid 

Relevant articles and documents

The first target specific, highly diastereoselective synthesis, design and characterization of pyranoquinolinyl acrylic acid diastereomers as potential α-glucosidase inhibitors

In the present investigation we report the first target specific, highly diastereoselective synthesis of new class of pyranoquinolinyl/furoquinolinyl-acrylic acid diastereomers and evaluation of their invitro α-glucosidase inhibitory activity. All the pro

Structural Effects of the Acidity of E-α-Phenyl-β-arylacrilic Acids

The dissociation equilibrium constants of some E-α-phenyl-β-arylacrilic acids (Ar=2-pyridyl, 3-pyridyl, 4-pyridyl, 1-naphthyl, 2-naphthyl, anthracen-9-yl) have been measured in 80percent aqeous 2-methoxyethanol at 25 deg C., The pKa values of these acids, together with those of p-substituted phenyl, 2-furyl, 2-thienyl and selenophen-2-yl derivitives, have been rationalized by an equation involving separate contributions of polar, conjugative and steric effects of heterocycles.The pKa values of some E-α-phenyl-β-alkylacrilic acids (alk=methyl; ethyl; n-propyl; i-propyl; n-butyl; i-butyl) are also reported.