836-79-3 Usage
Uses
Used in Chemical Synthesis:
1,1,1,3,3,3-HEXAFLUORO-2-(4-HYDROXYPHENYL)PROPAN-2-OL is used as a reactant in chemical synthesis for its ability to participate in various chemical reactions due to its fluorine and hydroxyphenyl groups.
Used in Polymer Production:
In the Polymer Industry, 1,1,1,3,3,3-HEXAFLUORO-2-(4-HYDROXYPHENYL)PROPAN-2-OL is used as a monomer or a building block for creating polymers with specific properties, leveraging its reactive fluorine and hydroxyphenyl components.
Used in Pharmaceutical Drug Development:
In the Pharmaceutical Industry, 1,1,1,3,3,3-HEXAFLUORO-2-(4-HYDROXYPHENYL)PROPAN-2-OL is used as an intermediate in the synthesis of pharmaceutical drugs, taking advantage of its complex structure to create new drug candidates with potential therapeutic applications.
Used in Material Science:
In the Material Science field, 1,1,1,3,3,3-HEXAFLUORO-2-(4-HYDROXYPHENYL)PROPAN-2-OL is used as a component in the development of advanced materials, such as coatings or adhesives, that benefit from the compound's unique chemical properties.
Note: The specific applications and industries mentioned above are hypothetical and provided as examples based on the general properties of the compound. The actual uses may vary depending on the specific context and research in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 836-79-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 836-79:
(5*8)+(4*3)+(3*6)+(2*7)+(1*9)=93
93 % 10 = 3
So 836-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F6O2/c10-8(11,12)7(17,9(13,14)15)5-1-3-6(16)4-2-5/h1-4,16-17H
836-79-3Relevant academic research and scientific papers
Fluorine-containing compound of fluorine-containing polymerizable monomer and its manufacturing method
-
Paragraph 0114, (2016/12/12)
PROBLEM TO BE SOLVED: To provide a method for producing a fluorine-containing polymerizable monomer, with which a fluorine-containing compound with a hydroxy fluoroalkyl group bonded to the para position thereof is obtained with high selectivity by making phenols and a fluorine-containing ketone react with each other. SOLUTION: A fluorine-containing compound of general formula (3) is obtained by making a compound of general formula (1) and a fluorine-containing ketone of general formula (2) react with each other in the presence of a fluorine-containing acid catalyst (in formulas, R1-R3respectively and independently represent a hydrogen atom, a straight chain, branched or cyclic alkyl group, an alkenyl group, and so on, and optionally have a fluorine or oxygen atom, R2and R3are optionally bonded to each other and either of them has a fluorine atom, X is an integer of 0-2, and Y is an integer of 0-8). COPYRIGHT: (C)2013,JPOandINPIT
Mechanisms for the Uncatalyzed and Hydrogen Ion Catalyzed Reactions of a Simple Quinone Methide with Solvent and Halide Ions
Richard, John P.
, p. 4588 - 4595 (2007/10/02)
The quinone methide 4-[bis(trifluoromethyl)methylene]cyclohexa-2,5-dienone (1) has been prepared in situ from the solvolysis of 4-MeOArC(CF3)2OTs in 50:50 (v/v) trifluoroethanol/water, and its reactions with solvent and halide ions h
