93041-45-3 Usage
Uses
Used in Pharmaceutical Industry:
3-(4-METHOXYPHENYL)-5-METHYL-4-ISOXAZOLECARBOXYLIC ACID is used as a building block for the synthesis of pharmaceuticals due to its versatile chemical structure and potential medicinal properties.
Used in Organic Chemistry:
3-(4-METHOXYPHENYL)-5-METHYL-4-ISOXAZOLECARBOXYLIC ACID is used as a key intermediate in the synthesis of various organic compounds, leveraging its reactivity and structural features.
Used in Anti-Inflammatory Applications:
3-(4-METHOXYPHENYL)-5-METHYL-4-ISOXAZOLECARBOXYLIC ACID is used as an anti-inflammatory agent, potentially aiding in the treatment of conditions characterized by inflammation.
Used in Anti-Bacterial Applications:
3-(4-METHOXYPHENYL)-5-METHYL-4-ISOXAZOLECARBOXYLIC ACID is used as an anti-bacterial agent, showing promise in combating bacterial infections.
Used in Medicinal Research:
3-(4-METHOXYPHENYL)-5-METHYL-4-ISOXAZOLECARBOXYLIC ACID is used in ongoing research for its potential medicinal applications, including the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 93041-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,4 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93041-45:
(7*9)+(6*3)+(5*0)+(4*4)+(3*1)+(2*4)+(1*5)=113
113 % 10 = 3
So 93041-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO4/c1-7-10(12(14)15)11(13-17-7)8-3-5-9(16-2)6-4-8/h3-6H,1-2H3,(H,14,15)
93041-45-3Relevant academic research and scientific papers
Isoxazolopyridone derivatives as allosteric metabotropic glutamate receptor 7 antagonists
Nakamura, Masayuki,Kurihara, Hideki,Suzuki, Gentaroh,Mitsuya, Morihiro,Ohkubo, Mitsuru,Ohta, Hisashi
scheme or table, p. 726 - 729 (2010/05/18)
This Letter describes the synthesis and evaluation of mGluR7 antagonists in the isoxazolopyridone series. In the course of modification in this class, novel solid support synthesis of the isoxazolopyridone scaffold was developed. Subsequent chemical modification led to the identification of several potent derivatives with improved physicochemical properties compared to a hit compound 1. Among these, 2 showed good oral bioavailability and brain penetrability, suggesting that 2 may be useful for in vivo study to elucidate the role of mGluR7.
