3189-40-0

Basic information

• Product Name: N-ethyl‐5‐hydroxyl‐2‐phenyl-1H-indole‐3‐ylcarboxylic acid
• Synonyms: N-ethyl‐5‐hydroxyl‐2‐phenyl-1H-indole‐3‐ylcarboxylic acid
• CAS NO: 3189-40-0
• Molecular Weight: 281.311
• Mol File: 3189-40-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-ethyl‐5‐hydroxyl‐2‐phenyl-1H-indole‐3‐ylcarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N-ethyl‐5‐hydroxyl‐2‐phenyl-1H-indole‐3‐ylcarboxylic acid(3189-40-0)
• EPA Substance Registry System: N-ethyl‐5‐hydroxyl‐2‐phenyl-1H-indole‐3‐ylcarboxylic acid(3189-40-0)

Safety Data

• Hazardous Substances Data: 3189-40-0(Hazardous Substances Data)

Upstream product

• 53256-19-2 ethyl (Z)-3-amino-3-phenylacrylate 
• 106-51-4 p-benzoquinone 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 33831-72-0 ethyl 3-amino-3-phenylprop-2-enoate 
• 124413-63-4 ethyl 3-amino-3-phenyl-2-propenoate 

Relevant articles and documents

Visible Light Promoted Synthesis of Indoles by Single Photosensitizer under Aerobic Conditions

The construction of substituted indole skeletons is always an important concern of synthetic chemists because of its prevalent structure found in natural products and biological molecules. Here, we succeeded in preparing indoles and their derivatives from

Tandem Blaise-Nenitzescu reaction: One-pot synthesis of 5-hydroxy-α-(aminomethylene)benzofuran-2(3H)-ones from nitriles

In contrast to the reaction of benzoquinones with β-enaminoesters providing indoles (Nenitzescu reaction), the tandem one-pot reaction of the Blaise reaction intermediate, zinc bromide complex of β-enaminoesters, with benzoquinone affords 5-hydroxy-α-(ami

Indolequinone antitumor agents: Correlation between quinone structure, rate of metabolism by recombinant human NAD(P)H:quinone oxidoreductase, and in vitro cytotoxicity

A series of indolequinones bearing various functional groups has been synthesized, and the effects of substituents on the metabolism of the quinones by recombinant human NAD(P)H: quinone oxidoreductase (NQO1) were studied. Thus 5-methoxyindolequinones wer