200956-55-4

Usage

Uses

Used in Pharmaceutical Development:
Benzamide, 3-bromo-4-methoxy-, is used as a building block in the development of pharmaceuticals for its potential applications in creating new drug molecules. Its structural versatility and reactivity allow for the synthesis of various compounds with potential therapeutic effects.
Used in Agrochemical Development:
Benzamide, 3-bromo-4-methoxy-, is also used as a building block in the development of agrochemicals. Its unique structure and reactivity contribute to the creation of new compounds with potential applications in agriculture, such as pesticides or herbicides.
Used in Organic Synthesis:
In the field of organic synthesis, benzamide, 3-bromo-4-methoxy-, serves as a valuable intermediate for the synthesis of various organic compounds. Its presence of a bromine atom and a methoxy group on the benzene ring allows for further functionalization and the formation of a wide range of derivatives with diverse properties and applications.

InChI:InChI=1/C8H8BrNO2/c1-12-7-3-2-5(8(10)11)4-6(7)9/h2-4H,1H3,(H2,10,11)

Upstream product

• 463-72-9 carbamic chloride 
• 578-57-4 2-bromoanisole 
• 637-69-4 4-Methoxystyrene 

Downstream Products

• 1448868-16-3 3-[5-(5-chloro-1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-6-(4-chloro-phenyl)-1-isopropyl-4-oxo-1,4,5,6-tetrahydro-pyrrolo[3,4-d]imidazol-2-yl]-4-methoxy-benzamide 
• 1448868-15-2 3-[5-(5-chloro-2-methyl-phenyl)-6-(4-chloro-phenyl)-1-isopropyl-4-oxo-1,4,5,6-tetrahydro-pyrrolo[3,4-d]imidazol-2-yl]-4-methoxy-benzamide 
• 1448868-14-1 3-[5-(3-chloro-2-fluoro-phenyl)-6-(4-chloro-phenyl)-1-isopropyl-4-oxo-1,4,5,6-tetrahydro-pyrrolo[3,4-d]imidazol-2-yl]-4-methoxy-benzamide 

Relevant academic research and scientific papers

1,3-Dibromo-5,5-dimethylhydantoin mediated oxidative amidation of terminal alkenes in water

A variety of terminal alkenes were converted to the corresponding amides in yields of 25 to 86% in water via treatment with 1,3-dibromo-5,5-dimethylhydantoin, followed by reaction with molecular iodine and aq. NH3 (or amine) in one pot. This metal- and organic solvent-free protocol is not only suitable for styrene derivatives, but also, for the first time, works well on terminal aliphatic alkenes.