501904-27-4 Usage
Uses
Used in Pharmaceutical Industry:
1,2-Benzisoxazole-6-carboxylic acid, 3-amino-, methyl ester (9CI) is used as a pharmaceutical intermediate for the development of anti-inflammatory and analgesic agents. Its unique structure and properties make it a promising candidate for the creation of new drugs that can effectively manage inflammation and pain.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1,2-Benzisoxazole-6-carboxylic acid, 3-amino-, methyl ester (9CI) is utilized as a key compound in the design and synthesis of novel therapeutic agents targeting neurodegenerative diseases. Its potential to modulate specific biological pathways and interact with cellular targets makes it a valuable tool in the search for effective treatments for such conditions.
Used in Chemical Synthesis:
1,2-Benzisoxazole-6-carboxylic acid, 3-amino-, methyl ester (9CI) serves as a versatile building block in organic synthesis. Its methyl ester group allows for further functionalization and modification, enabling the development of new chemical entities with diverse applications in various industries, including materials science, agrochemicals, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 501904-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,9,0 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 501904-27:
(8*5)+(7*0)+(6*1)+(5*9)+(4*0)+(3*4)+(2*2)+(1*7)=114
114 % 10 = 4
So 501904-27-4 is a valid CAS Registry Number.
501904-27-4Relevant academic research and scientific papers
Preparation of 2-hydroxybenzamidines from 3-aminobenzisoxazoles
Lepore, Salvatore D,Schacht, Aaron L,Wiley, Michael R
, p. 8777 - 8779 (2007/10/03)
2-Hydroxybenzamidines have been prepared from 3-aminobenzisoxazoles by reductive cleavage of the nitrogen-oxygen bond using catalytic hydrogenation, Zn/AcOH or NiCl2/NaBH4. This ring-opening reaction can be accomplished chemoselectively in the presence of a variety of hydrogenation-sensitive functional groups including an aryl bromide, benzyl carbamate, and olefin.
