59899-89-7 Usage
General Description
Methyl 2-(1,2-benzisoxazol-3-yl)acetate is a chemical compound that belongs to the class of benzisoxazoles, which are heterocyclic compounds containing a benzene ring fused to an isoxazole ring. METHYL 2-(1,2-BENZISOXAZOL-3-YL)ACETATE is an ester, with a methyl group attached to the acetyl group, and a benzisoxazolyl group attached to the carbon atom of the ester. It is commonly used as a building block in organic synthesis and pharmaceutical research, and has potential applications in the development of pharmaceuticals, agrochemicals, and materials science. Methyl 2-(1,2-benzisoxazol-3-yl)acetate may also have biological activities and pharmacological properties, making it a subject of interest for further research and development in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 59899-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,9 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59899-89:
(7*5)+(6*9)+(5*8)+(4*9)+(3*9)+(2*8)+(1*9)=217
217 % 10 = 7
So 59899-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c1-13-10(12)6-8-7-4-2-3-5-9(7)14-11-8/h2-5H,6H2,1H3
59899-89-7Relevant articles and documents
Novel Base-induced Reactions of Substituted (1,2-Benzisoxazol-3-yl)acetates
Ueda, Shozo,Naruto, Shunsuke,Yoshida, Toyokichi,Sawayama, Tadahiro,Uno, Hitoshi
, p. 1013 - 1022 (2007/10/02)
The reactions of substituted (1,2-benzisoxazol-3-yl)acetates with strong bases are described.The esters (1) and (2) having electron-donating and dialkylamino substituents undergo novel ring transformations on treatment with NaH, ButOK, or MeONa
