52817-13-7

Usage

Uses

Used in Organic Synthesis:
6-BROMO-3-CYANOCHROMONE is used as a key intermediate in the synthesis of various organic compounds due to its reactive functional groups, which facilitate multiple types of chemical reactions.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 6-BROMO-3-CYANOCHROMONE is utilized as a building block for the development of new drugs, leveraging its structural features to enhance the pharmacological properties of medicinal compounds.
Used in Material Science:
6-BROMO-3-CYANOCHROMONE is employed in the creation of novel materials, capitalizing on its chemical and physical properties to improve material performance in various applications.
Used in the Study of Organic Reactions:
6-BROMO-3-CYANOCHROMONE serves as a model in the investigation of organic reactions, providing insights into reaction mechanisms and the behavior of similar compounds under different conditions.
Overall, 6-BROMO-3-CYANOCHROMONE's diverse applications underscore its importance in the fields of chemistry and materials science, with potential for further expansion as new uses are discovered.

InChI:InChI=1/C10H4BrNO2/c11-8-1-2-9-6(4-8)3-7(5-12)10(13)14-9/h1-4H

Upstream product

• 1450-75-5 5-Bromo-2-hydroxyacetophenone 
• 68-12-2 N,N-dimethyl-formamide 
• 52817-12-6 6-bromo-4-oxo-4H-chromene-3-carbaldehyde 

Downstream Products

• 1380762-63-9 7-bromo-2-(4-methoxyphenyl)-5H-chromeno[2,3-d]pyrimidin-5-one 

Relevant academic research and scientific papers

Metal-free access to 3-allyl-2-alkoxychromanonesviaphosphine-catalyzed alkoxy allylation of chromones with MBH carbonates and alcohols

A metal-free access to 3-allyl-2-alkoxychromanones by PPh3-catalyzed alkoxy allylation of chromones with MBH carbonates and alcohols is described. This reaction is performed under mild conditions and it shows good functional group tolerance, providing a series of functionalized chromanones in moderate to high yields with excellent diastereoselectivities. Deuterium-labeling experiments to probe a possible mechanism and scale-up reaction were also conducted.

Substituted chromone-3-carbonitriles, carboxamides and carboxylic acids useful for preventing asthmatic symptoms

Substituted chromone-3-carbonitriles, carboxamides and carboxylic acids having the structural formula: SPC1 Wherein R1 represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, or acyloxy; R2 represents hydrogen, lower alkyl, fluorinated lower alkyl, alkoxycarbonyl, carboxy, or lower alkyl carboxylic acid; Z represents cyano, carboxy, alkoxycarbonyl, or EQU1 wherein X represents amino, N-lower-alkylamino, hydroxylamino, N-lower-alkylhydroxylamino, ureido, piperidino, or anilino, with the proviso that when R2 represents hydrogen, Z represents cyano or EQU2 wherein X has the same meaning as given above; and wherein R2 and Z together may form a substituted pyrrole ring; and the corresponding non-toxic, pharmaceutically acceptable salts.