73916-05-9 Usage
Uses
Used in Research and Development:
(E)-5-Methyl-2-styrylbenzoxazole is used as a fluorescent probe for detecting and quantifying metal ions in biological and environmental samples. Its application is crucial for understanding the role and concentration of metal ions in various scientific studies.
Used in Organic Synthesis:
(E)-5-Methyl-2-styrylbenzoxazole is used as a key intermediate in the synthesis of various organic compounds and materials. Its unique structure allows for the creation of new molecules with potential applications in different industries.
Used in Organic Electronic Devices:
(E)-5-Methyl-2-styrylbenzoxazole is used in the development of organic electronic devices due to its electronic properties. It can be integrated into the design of these devices to enhance their performance and functionality.
Used in Fluorescent Dyes for Biological Tracing:
(E)-5-Methyl-2-styrylbenzoxazole is used as a fluorescent dye for tracing biological molecules. Its ability to emit light upon interaction with specific molecules makes it a valuable tool in the field of biochemistry and molecular biology.
Used in Environmental Analysis:
(E)-5-Methyl-2-styrylbenzoxazole is used in environmental analysis to detect and quantify metal ions in samples. This application is essential for monitoring and managing the presence of potentially harmful metal ions in the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 73916-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,1 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73916-05:
(7*7)+(6*3)+(5*9)+(4*1)+(3*6)+(2*0)+(1*5)=139
139 % 10 = 9
So 73916-05-9 is a valid CAS Registry Number.
73916-05-9Relevant academic research and scientific papers
2-STYRYLBENZOXAZOLE DERIVATIVES
Arient, Josef
, p. 3160 - 3165 (2007/10/02)
A series of 35 derivatives of 2-styrylbenzoxazole I-XXXV with methyl, chloro, hydroxy, methoxy, dimethylamino, nitro, cyano and methoxycarbonyl substituents have been prepared by reaction of substituted 2-acetamidophenol with respective benzaldehyde derivatives.
