15847-18-4

Usage

Uses

Used in Analytical Chemistry:
7-AMINOFLAVONE 97 is used as a fluorescent probe for the detection of metal ions. Its fluorescent properties allow for sensitive and selective detection of various metal ions, making it a valuable tool in analytical chemistry.
Used in Pharmaceutical and Agrochemical Industries:
7-AMINOFLAVONE 97 serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique chemical structure contributes to the development of new drugs and agrochemical products.
Used in Cancer Research:
In the field of cancer research, 7-AMINOFLAVONE 97 is used for its potential anti-cancer properties. It is being investigated for its ability to target and inhibit the growth of cancer cells, offering a promising avenue for the development of new cancer therapies.
Used in Organic Light-Emitting Diodes (OLEDs):
7-AMINOFLAVONE 97 is also used as a component in organic light-emitting diodes (OLEDs). Its bright yellow color and solid-state properties make it suitable for use in the development of advanced display and lighting technologies.
Used in Research and Development:
7-AMINOFLAVONE 97 is utilized in research and development for its potential applications in various industries. Its unique properties and versatility make it an attractive candidate for further exploration and innovation.

InChI:InChI=1/C15H11NO2/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-9H,16H2

Upstream product

• 35820-45-2 7-nitro-2-phenyl-chromen-4-one 
• 36773-17-8 acetic acid-[3-hydroxy-4-(3-oxo-3-phenyl-propionyl)-anilide] 
• 856814-67-0 1-(2-hydroxy-4-nitro-phenyl)-3-phenyl-propane-1,3-dione 
• 14221-71-7 7-acetamidoflavone 

Downstream Products

• 1192308-02-3 2-methoxy-2-oxo-(S)-1-phenylethyl 2-[(4-oxo-2-phenyl-4H-chromen-7-yl)amino]-(R)-phenylacetate 
• 1394154-21-2 7-[2-(2-oxo-1-(piperazin-1-yl)propylidene)hydrazinyl]-2-phenyl-4H-chromen-4-one 
• 1394154-22-3 7-{2-[1-(4-methylpiperazin-1-yl)-2-oxopropylidene]hydrazinyl}-2-phenyl-4H-chromen-4-one 
• 1394154-23-4 7-{2-[1-(4-ethylpiperazin-1-yl)-2-oxopropylidene]hydrazinyl}-2-phenyl-4H-chromen-4-one 
• 1394154-25-6 7-{2-[1-(4-benzylpiperazin-1-yl)-2-oxopropylidene]hydrazinyl}-2-phenyl-4H-chromen-4-one 
• 1394154-27-8 ethyl 4-[2-oxo-1-(2-(4-oxo-2-phenyl-4H-chromen-7-yl)hydrazono)propyl]piperazine-1-carboxylate 
• 1394154-19-8 2-oxo-N-(4-oxo-2-phenyl-4H-chromen-7-yl)propanehydrazonoyl chloride 
• 1476774-69-2 [(η⁶-p-cymene)Ru(7-amino-2-phenyl-4H-benzopyran-4-one-κ¹-N)Cl₂] 

Relevant academic research and scientific papers

Buchwald-Hartwig reactions of monohaloflavones

The article describes the amination of different monobromo- or monochloroflavones with primary and secondary alkylamines and aniline derivatives by Buchwald-Hartwig reaction. The influence of the phosphine ligands used is described. The use of amino acid derivatives as a nitrogen source is also demonstrated. This latter reaction allows the synthesis of unique flavone-amino-acid conjugates.