18735-73-4 Usage
Uses
Used in Pharmaceutical Industry:
1-(2,5-diphenyl-1,3-oxazol-4-yl)ethanone is used as a building block for the synthesis of various pharmaceuticals and organic compounds due to its functional group reactivity. Its ability to form meta-depside bonds and its potential as a pharmacological agent with promising biological activities, including anti-inflammatory and anticancer properties, make it an interesting target for further research and development.
Used in Anticancer Applications:
In the field of oncology, 1-(2,5-diphenyl-1,3-oxazol-4-yl)ethanone is used as a pharmacological agent with potential anti-inflammatory and anticancer properties. Its reactivity and ability to modulate various oncological signaling pathways make it a promising candidate for the development of novel cancer treatments.
Used in Drug Delivery Systems:
To enhance the applications and efficacy of 1-(2,5-diphenyl-1,3-oxazol-4-yl)ethanone, especially in the context of cancer treatment, novel drug delivery systems have been developed. These systems employ various organic and metallic nanoparticles as carriers for the compound, aiming to improve its delivery, bioavailability, and therapeutic outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 18735-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,3 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18735-73:
(7*1)+(6*8)+(5*7)+(4*3)+(3*5)+(2*7)+(1*3)=134
134 % 10 = 4
So 18735-73-4 is a valid CAS Registry Number.
18735-73-4Relevant academic research and scientific papers
Photochemistry of 4-Acylisoxazoles
Sauers, R. R.,Hadel, L. M.,Scimone, A. A.,Stevenson, T. A.
, p. 4011 - 4019 (2007/10/02)
The photochemistry of 4-acylisoxazoles 4, 5, 13, 14, and 17 was investigated in an effort to clarify literature contradictions and anomalies and to provide a more detailed picture of the nature and number of intermediates involved in photoreactions of these systems.In contrast to a previous report on the photorearrangement of 14, both oxazoles expected from a 2H-azirine intermediate have been observed.Wavelength studies of 5 and the derived 2H-azirine 10 revealed evidence for the involvement of at least two distinct product-forming intermediates.The results of quantum yield and laser photolysis measurements for ketones 4, 14, and 17 have been interpreted in terms of rapid openings of triplet states to form diradical-like intermediates coupled with efficient reclosures (70-99percent).
