508182-19-2 Usage
Uses
Used in Pharmaceutical Research and Development:
3-(2-methoxyphenyl)-4,5-dihydroisoxazole-5-carboxylic acid (SALTDATA: FREE) is utilized as a key intermediate in the synthesis of drug candidates due to its potential therapeutic properties. Its presence in various compounds may contribute to anti-inflammatory, analgesic, or neuroprotective effects, making it a valuable asset in the development of new medications for a multitude of medical conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(2-methoxyphenyl)-4,5-dihydroisoxazole-5-carboxylic acid (SALTDATA: FREE) is employed as a structural component in the design and synthesis of novel compounds with potential therapeutic applications. Its unique chemical properties allow for the creation of molecules that can target specific biological pathways, offering new avenues for treatment of various diseases.
Used in Drug Discovery:
3-(2-methoxyphenyl)-4,5-dihydroisoxazole-5-carboxylic acid (SALTDATA: FREE) is leveraged in drug discovery processes to identify and optimize lead compounds with desired pharmacological properties. Its incorporation into diverse chemical structures facilitates the exploration of new chemical space, potentially leading to the discovery of innovative therapeutic agents.
Used in Biochemical Research:
In biochemical research, 3-(2-methoxyphenyl)-4,5-dihydroisoxazole-5-carboxylic acid (SALTDATA: FREE) serves as a valuable tool for studying the mechanisms of action and biological activities of various compounds. Its presence in experimental setups can provide insights into the interactions between molecules and their targets, aiding in the understanding of complex biological processes and the development of targeted therapies.
Overall, 3-(2-methoxyphenyl)-4,5-dihydroisoxazole-5-carboxylic acid (SALTDATA: FREE) is a versatile chemical entity with significant implications in the pharmaceutical and biomedical fields, driving advancements in drug development and therapeutic interventions.
Check Digit Verification of cas no
The CAS Registry Mumber 508182-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,8,1,8 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 508182-19:
(8*5)+(7*0)+(6*8)+(5*1)+(4*8)+(3*2)+(2*1)+(1*9)=142
142 % 10 = 2
So 508182-19-2 is a valid CAS Registry Number.
508182-19-2Relevant academic research and scientific papers
New fragmentation of 2-isoxazoline-5-carboxylic acid chlorides
Golebiewski,Gucma
, p. 509 - 513 (2007/10/03)
A novel base promoted degradation of 3-aryl-2-isoxazoline-5-carboxylic acid chlorides to aryl nitriles has been discovered.
