36238-83-2

Usage

Uses

As the provided materials do not specify the exact applications of 7-Methylbenzo[d]isoxazol-3-ol, it is not possible to list its uses in different industries or as an application type for a specific reason. Further research and investigation would be necessary to determine its potential uses and benefits in various fields.

InChI:InChI=1/C8H7NO2/c1-5-3-2-4-6-7(5)11-9-8(6)10/h2-4H,1H3,(H,9,10)

Upstream product

• 83-40-9 3-methylsalicylic acid 
• 23287-26-5 3-methylsalicylic acid methyl ester 
• 26071-07-8 2,N-dihydroxy-3-methylbenzamide 

Downstream Products

• 128520-86-5 3-chloro-7-methyl-1,2-benzisoxazole 
• 1299489-96-5 7-(2',4',5'-trifluoro-biphenyl-4-yl-oxymethyl)-benzo[d]isoxazol-3-ol 
• 1299490-07-5 7-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-benzo[d]isoxazol-3-ol 
• 1299490-13-3 7-(2'-chloro-4',5'-difluoro-biphenyl-4-yloxymethyl)-benzo[d]isoxazol-3-ol 
• 1299489-99-8 7-methyl-3-trityloxy-benzo[d]isoxazole 
• 1299490-20-2 7-(4',5'-difluoro-2'-methyl-biphenyl-4-yloxymethyl)-3-trityloxy-benzo[d]isoxazole 
• 1299490-15-5 7-(2'-chloro-4',5'-difluoro-biphenyl-4-yloxymethyl)-3-trityloxy-benzo[d]isoxazole 
• 1299490-10-0 7-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-3-trityloxy-benzo[d]isoxazole 
• 1299490-04-2 7-(2',4',5'-trifluoro-biphenyl-4-yl-oxymethyl)-3-trityloxy-benzo[d]isoxazole 
• 1299490-02-0 7-bromomethyl-3-trityloxy-benzo[d]isoxazole 
• 1299490-18-8 7-(4',5'-difluoro-2'-methyl-biphenyl-4-yloxymethyl)-benzo[d]isoxazol-3-ol 

Relevant academic research and scientific papers

Chromatography-free, Mitsunobu-triggered heterocyclizations of salicylhydroxamic acids to 3-hydroxybenzisoxazoles

The Mitsunobu reaction has become one of the most powerful tools to alkylate acidic pronucleophiles. A significant caveat of Mitsunobu chemistry, however, is that the reaction mixture is often plagued with purification problems owing to the phosphine oxide and hydrazine dicarboxylate by-products. In addition to the development of more readily separable Mitsunobu reagents, the product's physicochemical properties may be exploited to facilitate purification. In this regard, we present a swift and efficient preparation of 3-hydroxybenzisoxazoles by the Mitsunobu-triggered heterocyclizations of salicylhydroxamic acids, which can be isolated by an acid–base work-up. As expected, a range of functional groups was compatible with the chemistry.