57258-58-9 Usage
Uses
Used in Organic Chemistry:
2,4-dinitro-5-fluorophenylazide is used as a photolabile protecting group for amines and alcohols. The reason for its use is that upon exposure to light, the phenylazide group undergoes a photochemical reaction, leading to the release of the protected functional group. This makes it a valuable tool for the controlled release of biologically active compounds and for the study of complex molecular systems.
Used in Controlled Release Systems:
2,4-dinitro-5-fluorophenylazide is used as a component in the development of controlled release systems for biologically active compounds. The photolabile nature of the compound allows for the timed release of these compounds when exposed to light, which can be particularly useful in drug delivery and other applications requiring precise control over the release of active ingredients.
Used in Molecular Systems Research:
2,4-dinitro-5-fluorophenylazide is used as a research tool for studying complex molecular systems. Its photolabile properties enable scientists to manipulate and investigate the behavior of molecules under controlled conditions, which can provide insights into their structure, function, and interactions.
Safety Note:
It is crucial to handle 2,4-dinitro-5-fluorophenylazide with care due to its potential explosive nature. It should be used in a controlled laboratory environment with appropriate safety measures to ensure the safety of researchers and the integrity of the experiments.
Check Digit Verification of cas no
The CAS Registry Mumber 57258-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,5 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57258-58:
(7*5)+(6*7)+(5*2)+(4*5)+(3*8)+(2*5)+(1*8)=149
149 % 10 = 9
So 57258-58-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H2FN5O4/c7-3-1-4(9-10-8)6(12(15)16)2-5(3)11(13)14/h1-2H
57258-58-9Relevant academic research and scientific papers
Synthesis and fluorescence properties of 4,5-, 4,6- and 5,6-disubstituted benzofurazan (2,1,3-benzoxadiazole) compounds
Okiyama, Natsuko,Uchiyama, Seiichi,Onoda, Maki,Imai, Kazuhiro,Santa, Tomofumi
, p. 165 - 173 (2007/10/03)
New 4,5-, 4,6- and 5,6-disubstituted benzofurazan (2,1,3-benzoxadiazole) compounds having various substituent groups were synthesized. Their fluorescence properties were obtained and the discussions were made to develop new sensitive and selective fluores
