28202-32-6 Usage
Uses
Used in Organic Synthesis:
4-(1,1,2,2-TETRAFLUOROETHOXY)NITROBENZENE is used as an intermediate in the production of dyes, pigments, and pharmaceuticals due to its strong electron-withdrawing properties, which facilitate the synthesis of other fluorinated compounds.
Used in Materials Science:
In the field of materials science, 4-(1,1,2,2-TETRAFLUOROETHOXY)NITROBENZENE is used as a building block for the development of advanced polymers and coatings. Its fluorinated nature contributes to the unique properties of these materials, enhancing their performance in various applications.
Used in the Production of Advanced Polymers:
4-(1,1,2,2-TETRAFLUOROETHOXY)NITROBENZENE is used as a monomer in the synthesis of polymers with specific characteristics, such as enhanced chemical resistance and thermal stability, which are desirable in various industrial applications.
Used in the Development of Coatings:
4-(1,1,2,2-TETRAFLUOROETHOXY)NITROBENZENE is used as a component in the formulation of coatings that exhibit improved durability, resistance to environmental factors, and other performance-enhancing properties.
It is crucial to handle 4-(1,1,2,2-TETRAFLUOROETHOXY)NITROBENZENE with care, as it may pose hazards if not properly managed and controlled, ensuring safety in its applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 28202-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,0 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28202-32:
(7*2)+(6*8)+(5*2)+(4*0)+(3*2)+(2*3)+(1*2)=86
86 % 10 = 6
So 28202-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F4NO3/c9-7(10)8(11,12)16-6-3-1-5(2-4-6)13(14)15/h1-4,7H
28202-32-6Relevant academic research and scientific papers
Facile and efficient synthesis of fluoroalkyl aryl ethers
Kamal, Ahmed,Pratap,Ramana, K.Venkata,Ramana,Babu, A.Hari
, p. 7353 - 7355 (2007/10/03)
A convenient and practical method for the preparation of fluoroalkyl aryl ethers via substitution of iodoalkyl fluorides is described. This method involves KF complexation of the phenol, which increases the nucleophilicity of oxygen for the formation of the ether linkage.
CONDENSATION OF 1,2-DIBROMOTETRAFLUOROETHANE WITH VARIOUS POTASSIUM THIOPHENOXIDES AND PHENOXIDES
Rico, I.,Wakselman, C.
, p. 759 - 764 (2007/10/02)
BrCF2CF2Br reacts easily with various potassium thiophenoxides and phenoxides to give respectively 2-bromo tetrafluoroethyl thioethers and ethers.The lipophilicity of C6H5SCF2CF2Br and C6H5OCF2CF2Br is measured and compared with that of the well known C6H5SCF2CF2H and C6H5OCF2CF2H.
Urea derivatives and their use as herbicides
-
, (2008/06/13)
Compounds, useful as herbicides, of the formula SPC1 Wherein R1 is haloalkyl, halocycloalkyl, haloalkenyl, or halocycloalkenyl; n1 is 1 or 2; R4 is halogen, trifluoromethyl, alkyl, or alkoxy; n2 is 0, 1, 2, or 3; R2 is hydrogen or alkyl; and R3 is alkyl or alkoxy. Methods for making these compounds.
