2894-87-3 Usage
Uses
Used in Pharmaceutical Industry:
2,3,5,6-TETRAFLUORO-4-(PENTAFLUOROPHENYL)PHENOL is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3,5,6-TETRAFLUORO-4-(PENTAFLUOROPHENYL)PHENOL is utilized as a key intermediate in the production of agrochemicals, enhancing crop protection and yield.
Used in Materials Science:
2,3,5,6-TETRAFLUORO-4-(PENTAFLUOROPHENYL)PHENOL is employed as a precursor in the manufacturing of specialty fluorine-containing polymers, which are known for their unique properties such as high thermal stability, chemical resistance, and non-stick characteristics.
Used in Chemical Synthesis:
As a versatile chemical intermediate, 2,3,5,6-TETRAFLUORO-4-(PENTAFLUOROPHENYL)PHENOL is used in the synthesis of various compounds for research and industrial applications, expanding the scope of chemical innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 2894-87-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2894-87:
(6*2)+(5*8)+(4*9)+(3*4)+(2*8)+(1*7)=123
123 % 10 = 3
So 2894-87-3 is a valid CAS Registry Number.
InChI:InChI=1/C12HF9O/c13-3-1(4(14)8(18)9(19)7(3)17)2-5(15)10(20)12(22)11(21)6(2)16/h22H
2894-87-3Relevant academic research and scientific papers
Batsanov, Andrei S.,Brooke, Gerald M.,Holling, Darren,Kenwright, Alan M.
, p. 1731 - 1734 (2000)
The pyrolysis reaction of nonafluorobiphenyl-4-yl prop-2-enyl ether were studied. The reaction was proposed as a remarkable rearrangement reaction of an intramolecular Diels-Alder product. The flash vapor pyrolysis of the compound performed at 350 °C gave a complex mixture containing the products obtained from Diels-Alder reactions. The molecular structure of the compounds obtained was characterized by x ray crystallography.
Batsanov, Andrei S.,Brooke, Gerald M.,Holling, Darren,Kenwright, Alan M.
, p. 1549 - 1550 (1999)
The formation of the unexpected bicyclic compound 16 via the pyrolytic isomerisation of 4-nonafluorobiphenyl prop-2-enyl ether 8 can be rationalised by invoking the intermediacy of a rare retro-cyclisation reaction of the internal Diels-Alder adduct 12 (f
