503169-76-4 Usage
Description
2-(Bromomethyl)hexafluoropropan-2-ol, with the molecular formula C6H2BrF6O, is a halogenated alcohol and a member of the fluoroalkyl compounds class. This chemical compound is characterized by the presence of bromine and fluorine atoms in its structure, which impart it with unique chemical and physical properties. These properties make it a valuable compound for a variety of industrial and research applications.
Uses
Used in Pharmaceutical Industry:
2-(Bromomethyl)hexafluoropropan-2-ol is used as a building block for the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential applications in various therapeutic areas.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(Bromomethyl)hexafluoropropan-2-ol is utilized as a precursor in the production of agrochemicals. Its properties can contribute to the creation of novel pesticides or other agricultural chemicals that can improve crop protection and yield.
Used in Materials Science:
2-(Bromomethyl)hexafluoropropan-2-ol is also used in materials science for the synthesis of new materials with specific properties. Its fluorinated nature can lead to the development of materials with enhanced chemical resistance, thermal stability, or other desirable characteristics for various applications.
As with any chemical compound, it is essential to follow proper handling and safety precautions when working with 2-(bromomethyl)hexafluoropropan-2-ol to ensure the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 503169-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,1,6 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 503169-76:
(8*5)+(7*0)+(6*3)+(5*1)+(4*6)+(3*9)+(2*7)+(1*6)=134
134 % 10 = 4
So 503169-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H3BrF6O/c5-1-2(12,3(6,7)8)4(9,10)11/h12H,1H2
503169-76-4Relevant articles and documents
Facile preparation and synthetic applications of LiCH2C(CF3)2Oli
Grushin, Vladimir V.,Marshall, William J.,Halliday, Gary A.,Davidson, Fredric,Petrov, Viacheslav A.
, p. 121 - 129 (2007/10/03)
Bromohydrin BrCH2C(CF3)2OH readily reacts with two equivalents of n-BuLi at - 78 °C to produce the corresponding dilithium derivative LiCH2C(CF3)2OLi in high yield. This dilithiated derivative reacts selectively, acting as a C-nucleophile, with a variety of electrophiles such as R2PCl, carbonyl compounds, and epoxides, to give electron-deficient phosphines R2PCH2C(CF3)2OH, 1,3- and 1,4-diols, correspondingly.
