23464-97-3 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(5-Phenyl-2-oxazolyl)benzoic acid is used as a key building block for the synthesis of various pharmaceuticals due to its unique chemical structure and reactivity, facilitating the creation of new drugs with potential therapeutic benefits.
Used in Treatment of Inflammatory Conditions:
In the medical field, 2-(5-Phenyl-2-oxazolyl)benzoic acid is used as an anti-inflammatory and analgesic agent for managing conditions such as rheumatoid arthritis and inflammatory pain, leveraging its capacity to modulate inflammatory responses and alleviate discomfort.
Used in Materials Science for Optical and Electronic Devices:
2-(5-Phenyl-2-oxazolyl)benzoic acid is utilized as a photoluminescent material in the development of advanced optical and electronic devices, capitalizing on its light-emitting properties to enhance device performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 23464-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,6 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23464-97:
(7*2)+(6*3)+(5*4)+(4*6)+(3*4)+(2*9)+(1*7)=113
113 % 10 = 3
So 23464-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H11NO3/c18-16(19)13-9-5-4-8-12(13)15-17-10-14(20-15)11-6-2-1-3-7-11/h1-10H,(H,18,19)/p-1
23464-97-3Relevant academic research and scientific papers
SYNTHESIS AND STRUCTURE OF STERICALLY CROWDED POLYNUCLEAR ARYL DERIVATIVES OF FIVE-MEMBERED N-HETEROCYCLES, ORTHO ANALOGS OF POPOP
Doroshenko, A. O.,Patsenker, L. D.,Baumer, B. N.,Chepeleva, L. V.,Vankevich, A. V.,et al.
, p. 588 - 593 (2007/10/02)
Three sterically crowded polynuclear aryl derivatives of five-membered N-heterocycles, viz. ortho analogs of 1,4-bis(5-phenyloxazol-2-yl)benzene (POPOP), were synthesized and their structure studied by x-ray structure analysis and IR and Raman spectroscop
Aromatic Carbonylation Regio-Controlled by Oxazole and Isoxazole Rings, Novel Route to Heterocycle-Substituted o-Benzoates
Sakakibara, Tsutomu,Kume, Takashi,Ohyabu, Takahiro,Hase, Tsunao
, p. 1694 - 1697 (2007/10/02)
3,5-Diphenylisoxazole and 2,5-diphenyloxazole were regioselectively carbonylated under an atmosphere of carbon monoxide after the formation of arylpalladium(II) intermediates, to give bioactive o-benzoates substituted by isoxazole and oxazole rings in goo
