36238-83-2 Usage
General Description
7-Methylbenzo[d]isoxazol-3-ol is a chemical compound that falls under the category of organic compounds known as benzisoxazoles. These are aromatic compounds containing a benzene ring fused to an isoxazole ring. Not much information is readily available regarding its specific uses, properties, or toxicity. It is not a widely researched or commonly used chemical. Like many other chemicals, it is likely to require careful handling and specific storage conditions to maintain its stability and prevent its degradation. Its unique structure could potentially make it useful in the production of various synthetic materials or pharmaceuticals, although further research would be needed to confirm this.
Check Digit Verification of cas no
The CAS Registry Mumber 36238-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,3 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36238-83:
(7*3)+(6*6)+(5*2)+(4*3)+(3*8)+(2*8)+(1*3)=122
122 % 10 = 2
So 36238-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO2/c1-5-3-2-4-6-7(5)11-9-8(6)10/h2-4H,1H3,(H,9,10)
36238-83-2Relevant articles and documents
Chromatography-free, Mitsunobu-triggered heterocyclizations of salicylhydroxamic acids to 3-hydroxybenzisoxazoles
Van Eker, Daniel,Chauhan, Jay,Murphy, William A.,Conlon, Ivie L.,Fletcher, Steven
, p. 5301 - 5303 (2016/11/16)
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.
