14688-28-9 Usage
Uses
Used in Organic Synthesis:
(3,5-diphenyl-1,2-oxazol-4-yl)(phenyl)methanone is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for multiple points of reactivity, making it suitable for the synthesis of a broad range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3,5-diphenyl-1,2-oxazol-4-yl)(phenyl)methanone is utilized as a starting material for the development of new medications. Its potential biological activity and chemical versatility make it an attractive candidate for the design and synthesis of novel drug molecules targeting various therapeutic areas.
Used in Medicinal Chemistry:
(3,5-diphenyl-1,2-oxazol-4-yl)(phenyl)methanone serves as a valuable building block in medicinal chemistry, where it can be used to construct and optimize the structure of drug candidates. Its presence in a molecule can influence pharmacokinetic and pharmacodynamic properties, contributing to the overall effectiveness and safety of potential drugs.
Used in Chemical Research:
(3,5-diphenyl-1,2-oxazol-4-yl)(phenyl)methanone is also employed in chemical research to study the reactivity and properties of oxazole-containing molecules. Understanding its behavior in various chemical reactions can provide insights into the development of new synthetic methods and the discovery of new chemical entities with useful applications.
Check Digit Verification of cas no
The CAS Registry Mumber 14688-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,8 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14688-28:
(7*1)+(6*4)+(5*6)+(4*8)+(3*8)+(2*2)+(1*8)=129
129 % 10 = 9
So 14688-28-9 is a valid CAS Registry Number.
14688-28-9Relevant academic research and scientific papers
Enolate-mediated 1,3-dipolar cycloaddition reaction of β-functionalized ketones with nitrile oxides: Direct access to 3,4,5-trisubstituted isoxazoles
Zhou, Xiao,Xu, Xianhong,Shi, Zhenyan,Liu, Kun,Gao, Hua,Li, Wenjun
supporting information, p. 5246 - 5250 (2016/07/06)
TMG-catalyzed [3 + 2] organocatalytic 1,3-dipolar cycloaddition reactions of β-functionalized ketones with nitrile oxides have been developed. This strategy could generate 3,4,5-trisubstituted isoxazoles in high yields and regioselectivities.
Iron(III) chloride/diorganyl diselenides: A tool for intramolecular cyclization of alkynone O-methyloximes
Speran?a, Adriane,Godoi, Benhur,Zeni, Gilson
, p. 1630 - 1637 (2013/03/28)
This report describes the synthesis of 4-organoselenylisoxazoles via FeCl3/RSeSeR-mediated intramolecular cyclization of alkynone O-methyloximes. The optimized conditions allowed the cyclization to proceed at room temperature under ambient atmo
Formation of 4-Benzamidoisoxazole Derivatives
Zen, Shonosuke,Harada, Kazuho,Nakamura, Hikaru,Iitaka, Yoichi
, p. 2881 - 2884 (2007/10/02)
The titled compounds (3) were synthesized by the reaction of nitrile oxides with 1-azirines and also the reaction of aliphatic nitro compounds with dibenzoylmethane derivatives in the presence of acetyl chloride and sodium methoxide.The structure of 3 was
