239137-39-4

Usage

Uses

Used in Pharmaceutical Industry:
3-Amino-4-bromopyridine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structures of potential drug candidates. Its presence in these compounds can contribute to their therapeutic properties, making it an essential component in drug discovery and development.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Amino-4-bromopyridine is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its unique structure allows for the creation of compounds that can effectively control, repel, or kill unwanted organisms in agricultural settings.
Used in Research and Development:
3-Amino-4-bromopyridine is employed as a valuable intermediate in the research and development of new drug candidates. Its potential use in the treatment of various diseases, including cancer and inflammation, makes it a promising compound for further exploration and innovation in medicinal chemistry.
Used in Organic Synthesis:
As a building block in organic synthesis, 3-Amino-4-bromopyridine is used to produce a wide range of chemical compounds. Its reactivity and structural features make it suitable for various chemical reactions, facilitating the creation of new molecules with diverse applications across different industries.

InChI:InChI=1/C3H6F2O/c1-3(4,5)2-6/h6H,2H2,1H3

Upstream product

• 39910-67-3 4-azidopyridine 

Downstream Products

• 239137-45-2 4-Bromo-3-(2-bromoanilino)pyridine 
• 928008-25-7 tert-butyl {(7R,8R)-8-(2,4,5-trifluorophenyl)-6,7,8,9-tetrahydropyrido[3',4':4,5]imidazo[1,2-a]pyridin-7-yl}carbamate 
• 105752-11-2 4-iodopyridin-3-amine 
• 2922-07-8 2-phenyl-1H-pyrrolo[2,3-c]pyridine 
• 1395415-53-8 N-(4-bromo-pyridin-3-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamide 
• 1395414-17-1 N-[4-(2,4-dimethyl-thiazol-5-yl)-pyridin-3-yl]-N-methyl-3,5-bis-trifluoromethyl-benzamide 
• 1395412-59-5 N-[4-(5-fluoro-2-methoxy-phenyl)-pyridin-3-yl]-N-methyl-3,5-bis-trifluoromethyl-benzamide 
• 1395412-55-1 N-[4-(3,6-dimethoxy-pyridazin-4-yl)-pyridin-3-yl]-N-methyl-3,5-bis-trifluoromethyl-benzamide 
• 1395412-24-4 N-[4-(2-fluoro-phenyl)-pyridin-3-yl]-N-methyl-3,5-bis-trifluoromethyl-benzamide 
• 239137-49-6 4-Bromo-3-[2-bromo-N-(methylsulfonyl)anilino]pyridine 
• 244-63-3 betacarboline 
• 239137-41-8 4-bromo-N-phenylpyridin-3-amine 
• 7266-32-2 9H-pyrrolo[2,3-b:5,4-c']dipyridine 

Relevant academic research and scientific papers

PHOTOLYSIS OF PYRIDYL, QUINOLYL, AND ISOQUINOLYL AZIDES IN HYDROHALOGENOIC ACIDS

Photolysis of 4-azido-pyridine and -quinoline in hydrohalogenoic acids gave the 3-amino-4-halogeno compounds (2) via azirine or azacycloheptatetraene intermediates, whereas their N-oxides (4), under similar conditions, gave the 4-amino-3-halogeno compounds (5) presumably via nitrenium ion intermediates.In the 3-azidoquinoline and 4-azidoisoquinoline series, both free bases (6a, 8a) and N-oxides (6b, 8b) gave similar results to 4-azidopyridine and -quinoline N-oxides (4).