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Usage

Uses

Used in Pharmaceutical Industry:
7-Bromo-3-methylbenzo[d]isoxazole is used as a building block for synthesizing various bioactive compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 7-Bromo-3-methylbenzo[d]isoxazole serves as a key component in the synthesis of bioactive molecules, potentially leading to the creation of novel pesticides or other agrochemical products.
Used in Neuroprotective and Anti-Inflammatory Research:
7-Bromo-3-methylbenzo[d]isoxazole is used as a subject of study for its potential neuroprotective and anti-inflammatory properties, which could lead to advancements in the treatment of neurological disorders and inflammatory conditions.
Used as a Tool Compound in Biological Research:
This chemical is also utilized as a tool compound for targeting specific biological pathways, aiding researchers in understanding complex biological mechanisms and developing targeted therapies.

Upstream product

• 95-56-7 2-hydroxybromobenzene 
• 42524-23-2 2-Hydroxy-3-bromacetophenonoxim 
• 1836-05-1 3’-bromo-2’-hydroxylacetophenone 

Relevant academic research and scientific papers

Discovery of novel 3-{[(5,5-dimethyl-4,5-dihydroisoxazol-3-yl)sulfonyl]methyl}benzo[d]isoxazole analogs as promising very long chain fatty acids inhibitors

Very long chain fatty acids (VLCFAs) are one of the most principal and promising targets for herbicides discovery. In order to explore and find novel VLCFAs inhibitors with higher herbicidal activity and improved crop safety, a variety of new 3-{[(5,5-dimethyl-4,5-dihydroisoxazol-3-yl)sulfonyl]methyl}benzo[d]isoxazole derivatives were reasonably designed and synthesized. The results of greenhouse experiments indicated that several compounds exhibited good herbicidal activity against Digitaria sanguinalis, Echinochloa crus-galli, and Setaria faberii at rates of 150 g ai/ha. Compounds g4 and h1 displayed promising herbicidal activity against D sanguinalis and E crus-galli at rates of 75 g ai/ha, which is better than commercial pyroxasulfone and S-metolachlor. Moreover, compound h1 displayed higher activity against E crus-galli, D sanguinalis, and S faberii than pyroxasulfone and S-metolachlor even at a rate of 37.5 and 18.75 g ai/ha. Furthermore, both of the compounds g4 and h1 were much safer to these tested crops, especially to rice, wheat and rape, at the rate of 150 g ai/ha than pyroxasulfone. Therefore, h1 may act as a new lead structure for novel herbicides discovery.