24097-19-6 Usage
Description
3-(4-Chlorophenyl)-5-(4-methoxyphenyl)isoxazole is a chemical compound with the molecular formula C16H12ClNO2. It is an isoxazole derivative that features both a chlorophenyl and a methoxyphenyl group. 3-(4-Chlorophenyl)-5-(4-methoxyphenyl)isoxazole is known for its potential pharmacological and biological activities, with the chlorophenyl group possibly enhancing its interactions with biological targets and the methoxyphenyl group influencing its solubility and bioavailability. Further research is essential to explore the full spectrum of its applications and effects.
Uses
Used in Pharmaceutical Research and Development:
3-(4-Chlorophenyl)-5-(4-methoxyphenyl)isoxazole is utilized as a compound in pharmaceutical research and development due to its potential pharmacological and biological activities. The presence of the chlorophenyl and methoxyphenyl groups may contribute to its efficacy in targeting specific biological pathways or receptors, making it a promising candidate for the development of new drugs.
Used in Chemical Synthesis:
In the chemical synthesis industry, 3-(4-Chlorophenyl)-5-(4-methoxyphenyl)isoxazole can be used as a building block or intermediate in the synthesis of more complex molecules with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Used in Biological Research:
3-(4-Chlorophenyl)-5-(4-methoxyphenyl)isoxazole is employed as a research tool in biological studies to investigate its interactions with biological targets and understand its potential effects on cellular processes. This can provide valuable insights into the compound's mechanism of action and its suitability for therapeutic applications.
Note: The specific applications and industries for 3-(4-Chlorophenyl)-5-(4-methoxyphenyl)isoxazole are not explicitly mentioned in the provided materials. The uses listed above are inferred based on the compound's properties and potential activities. Further research and development are necessary to fully explore and validate its applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 24097-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,9 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24097-19:
(7*2)+(6*4)+(5*0)+(4*9)+(3*7)+(2*1)+(1*9)=106
106 % 10 = 6
So 24097-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H12ClNO2/c1-19-14-8-4-12(5-9-14)16-10-15(18-20-16)11-2-6-13(17)7-3-11/h2-10H,1H3
24097-19-6Relevant articles and documents
Aerobic oxidative synthesis of 3,5-disubstituted isoxazoles directly from α,β-unsaturated ketones
Li, Zheng,Wen, Gong,Fu, Rugang,Yang, Jingya
, p. 643 - 644 (2016/10/22)
Using an efficient aerobic oxidative method, the synthesis of ten 3,5-disubstituted isoxazoles by treatment of α,β-unsaturated ketones with hydroxylamine and NaOH at room temperature has been achieved.
Convenient synthesis of 3,5-disubstituted isoxazoles
Kurangi, Reshma F.,Kawthankar, Rima,Sawal, Sulfala,Desai, Vidya G.,Tilve, Santosh G.
, p. 587 - 589 (2007/10/03)
α,β-Unsaturated oximes obtained from the corresponding α,β-unsaturated ketones on treatment with 2 equivalents of manganese dioxide in refluxing chloroform gives 3,5-disubstituted isoxazoles in good yields. Copyright Taylor & Francis Group, LLC.
