1992-15-0 Usage
Uses
Used in Pharmaceutical Industry:
1,4-BIS(2-HYDROXYHEXAFLUOROISOPROPYL)BENZENE is used as a building block for the synthesis of high-performance polymers and specialty materials, contributing to the development of innovative pharmaceutical products.
Used in Electronics Industry:
In the electronics sector, 1,4-BIS(2-HYDROXYHEXAFLUOROISOPROPYL)BENZENE is utilized as a component in the production of surfactants and materials with specific properties required for electronic applications, such as heat resistance and chemical stability.
Used in Aerospace Industry:
1,4-BIS(2-HYDROXYHEXAFLUOROISOPROPYL)BENZENE is employed as a key intermediate in the creation of materials with exceptional performance characteristics, such as lightweight and high-strength polymers, suitable for aerospace applications.
Due to its fluorinated nature, it is crucial to handle and dispose of 1,4-BIS(2-HYDROXYHEXAFLUOROISOPROPYL)BENZENE with care to mitigate potential environmental and health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 1992-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1992-15:
(6*1)+(5*9)+(4*9)+(3*2)+(2*1)+(1*5)=100
100 % 10 = 0
So 1992-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H6F12O2/c13-7(9(15,16)17,11(21,22)25)5-1-2-6(4-3-5)8(14,10(18,19)20)12(23,24)26/h1-4,25-26H
1992-15-0Relevant academic research and scientific papers
Convenient syntheses of 1,1,1,3,3,3-hexafluoro-2-organyl-propan-2-ols and the corresponding trimethylsilyl ethers
Babadzhanova,Kirij,Yagupolskii,Tyrra,Naumann
, p. 1813 - 1819 (2007/10/03)
A new convenient synthetic procedure to obtain various 1,1,1,3,3,3- hexafluoro-2-organyl-propan-2-ols and the corresponding trimethylsilyl ethers has been worked out starting from anhydrides or activated esters of carboxylic acids and trimethyl(trifluoromethyl)silane in the presence of tetramethylammonium fluoride. Conditions for the selective formation of 1,1,1,3,3,3-hexafluoro-2-organyl-propan-2-ols as well as the trimethylsilyl derivatives have been found.
PERFLUOROALKYLATION OF BENZENE DERIVATIVES. AN IMPROVED SYNTHESIS OF 1,3-BIS(2-HYDROXYHEXAFLUORO-2-PROPYL)-5-(PERFLUORO-n-ALKYL)BENZENES
Sepiol, Janiusz,Soulen, Robert L.
, p. 61 - 74 (2007/10/02)
A three-step high yield synthesis of various 1,3-bis(2-hydroxyhexafluoro-2-propyl)-5-perfluoro-n-alkyl) benzenes is described.Significant improvements in the iodination and perfluoro-alkylation of a perfluoroalkylbenzene diol have been achieved.Copper coupling of straight-chain perfluoroalkyl iodides with the iodobenzene derivative in DMSO gave the desired compounds as DMSO complexes in 78-91 percent yield.
