14677-93-1 Usage
General Description
(5-methyl-3-phenyl-1,2-oxazol-4-yl)(phenyl)methanone, also known as oxazole, is a chemical compound with a molecular formula C15H11NO2. It is a heterocyclic compound containing both nitrogen and oxygen atoms in its ring structure. Oxazole is commonly used in the pharmaceutical industry as a building block in the synthesis of various drugs and bioactive molecules. It possesses interesting biological properties and has been reported to exhibit anticancer, antimicrobial, and antifungal activities. Oxazole derivatives have also been investigated for their potential use as fluorescent dyes and laser dyes due to their unique photophysical properties. Additionally, oxazole and its derivatives are of interest in the field of materials science for their potential use in organic electronic devices and sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 14677-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,7 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14677-93:
(7*1)+(6*4)+(5*6)+(4*7)+(3*7)+(2*9)+(1*3)=131
131 % 10 = 1
So 14677-93-1 is a valid CAS Registry Number.
14677-93-1Relevant 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).
