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5,7-Difluoro-6-bromoquinoline is an organic compound that is commonly used in the chemical industry.
It is a white or slightly yellowish solid that is soluble in water and organic solvents.
The compound is commonly used as an intermediate in the synthesis of various chemical products, both upstream and downstream.
Upstream products refer to the compounds that are used as raw materials to produce 5,7-Difluoro-6-bromoquinoline.
One of the most common upstream products is 6-bromoquinoline-2-carboxylic acid, which is converted to 5,7-Difluoro-6-bromoquinoline through a series of chemical reactions.
Other upstream products include bromodomains, which are structural motifs found in many proteins that recognize and bind to bromodomain-containing proteins.
Downstream products, on the other hand, refer to the chemical products that are produced using 5,7-Difluoro-6-bromoquinoline as a starting material.
One of the most common downstream products is the antibiotic rifamycin, which is used to treat a variety of bacterial infections.
Another downstream product is the anti-inflammatory drug siraspidine, which is used to treat inflammatory conditions such as rheumatoid arthritis.
Other downstream products include a variety of research chemicals, which are used by scientists to study the behavior of various proteins, enzymes, and other biological molecules.
These research chemicals are often used as tools for protein biochemistry, cell biology, and molecular biology.
The production of 5,7-Difluoro-6-bromoquinoline involves several steps, including its synthesis from 6-bromoquinoline-2-carboxylic acid and its conversion to rifamycin or siraspidine.
The synthesis of 5,7-Difluoro-6-bromoquinoline typically involves the use of organic solvents such as dichloromethane or chloroform, as well as various chemical reagents such as sodium hydroxide, hydrogen chloride, and sodium carbonate.
The synthesis of 5,7-Difluoro-6-bromoquinoline is usually performed in a multi-step process that involves several intermediate steps.
The first step involves the synthesis of 6-bromoquinoline-2-carboxylic acid from 6-bromoquinoline-2- nitrobenzene, which is followed by its conversion to 5,7-Difluoro-6-bromoquinoline through a series of chemical reactions.
The conversion of 5,7-Difluoro-6-bromoquinoline to rifamycin or siraspidine typically involves a series of chemical reactions, including substitution reactions, condensation reactions, and oxidation reactions.
These reactions are typically carried out in the presence of various chemical catalysts, such as palladium catalysts, and are often performed in a solvent such as ethyl acetate or acetonitrile.
Overall, the production of 5,7-Difluoro-6-bromoquinoline and its conversion to downstream products such as rifamycin and siraspidine is an important process in the chemical industry.
These products have a wide range of applications in medicine, agriculture, and other fields, making them valuable tools for researchers and drug developers.
As the field of organic synthesis continues to evolve, new and more efficient methods for the production of 5,7-Difluoro-6-bromoquinoline and its downstream products are likely to be developed, further expanding the reach and impact of this important class of compounds.