57554-57-1 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(1,1-Difluoroethyl)-2-nitrobenzene is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows for the creation of new medicinal compounds with potential therapeutic benefits.
Used in Agrochemical Production:
In the agrochemical industry, 1-(1,1-Difluoroethyl)-2-nitrobenzene is utilized as a starting material for the development of novel agrochemicals. Its properties contribute to the formulation of effective products for agricultural applications.
Used in Organic Electronics:
1-(1,1-Difluoroethyl)-2-nitrobenzene also holds potential in the field of organic electronics. It can be employed as a component in the design and synthesis of organic electronic materials, such as in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).
Used in Materials Science:
1-(1,1-Difluoroethyl)-2-nitrobenzene's properties make it a valuable asset in materials science, where it can be used to develop new materials with specific characteristics for various applications, including coatings, adhesives, and polymers.
It is crucial to handle 1-(1,1-Difluoroethyl)-2-nitrobenzene with care due to its potential health and environmental risks. Proper safety measures and precautions should be taken during its production, use, and disposal to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 57554-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,5 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57554-57:
(7*5)+(6*7)+(5*5)+(4*5)+(3*4)+(2*5)+(1*7)=151
151 % 10 = 1
So 57554-57-1 is a valid CAS Registry Number.
57554-57-1Relevant academic research and scientific papers
Scalable Approach to Fluorinated Heterocycles with Sulfur Tetrafluoride (SF4)
Ahunovych, Volodymyr,Boretskyi, Andrii,Bugera, Maksym,Klipkov, Anton A.,Mykhailiuk, Pavel K.,Razhyk, Bohdan,Semenov, Sergey,Tarasenko, Karen,Trofymchuk, Serhii
, p. 12181 - 12198 (2021/09/13)
A general approach to fluorinated (hetero)aromatic derivatives is elaborated. The key reaction is a deoxofluorination of substituted acetophenones with sulfur tetrafluoride (SF4). In contrast to previous deoxofluorination methods, this transformation is fast, scalable (up to 70 g), and high-yielding. More than 100 novel or previously hardly accessible fluorinated heterocycles, interesting for medicinal chemistry and agrochemistry, were synthesized.
