63539-54-8 Usage
Derivative of pyrrole
1H-Pyrrole-2,5-dione, 1-(2,3,5,6-tetrafluorophenyl)is derived from the pyrrole structure, which is a five-membered aromatic ring containing one nitrogen atom.
Class of organic compounds
Pyrrole-2,5-diones 1H-Pyrrole-2,5-dione, 1-(2,3,5,6-tetrafluorophenyl)- belongs to the class of pyrrole-2,5-diones, which are characterized by the presence of a pyrrole ring with two oxygen atoms double-bonded to adjacent carbon atoms.
Tetrafluorophenyl group
A phenyl ring with four fluorine atoms attached The presence of this group imparts unique chemical and physical properties to the compound.
Unique chemical and physical properties
The tetrafluorophenyl group provides the compound with distinct properties, making it suitable for various applications.
Applications
Synthesis of pharmaceuticals, agrochemicals, and electronic materials The compound can be used in the production of various products in different industries.
Building block for complex organic molecules
The compound can be employed as a building block in the construction of more complex organic molecules, which is useful in chemical research and development.
Versatile chemical compound
1H-Pyrrole-2,5-dione, 1-(2,3,5,6-tetrafluorophenyl)has potential uses in different industries due to its unique properties and versatility.
Check Digit Verification of cas no
The CAS Registry Mumber 63539-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,3 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63539-54:
(7*6)+(6*3)+(5*5)+(4*3)+(3*9)+(2*5)+(1*4)=138
138 % 10 = 8
So 63539-54-8 is a valid CAS Registry Number.
63539-54-8Relevant academic research and scientific papers
1H, 13C, and 19F NMR studies of phencyclone adducts of N-(polyhalophenyl)maleimides: Evidence for dynamic NMR in maleamic acids - Ab initio calculations for optimized structures
Marshall, Kimberly,Rosmarion, Kerstin,Sklyut, Olga,Azar, Nikolay,Callahan, Ronald,Rothchild, Robert
, p. 1893 - 1907 (2007/10/03)
NMR methods, including one- and two-dimensional techniques (at 7.05 T) for 1H, 13C and 19F, have been applied to studies of hindered rotations and magnetic anisotropy in some crowded Diels-Alder adducts of phencyclone (1).
