77253-67-9 Usage
Description
2,2,2-TRIFLUOROETHANOL-D3 is a deuterated form of 2,2,2-trifluoroethanol, a compound characterized by the presence of three fluorine atoms attached to an ethyl group. It is a versatile and valuable reagent in various chemical and biochemical applications due to its unique properties, such as its ability to mimic the hydrophobic effect and its use as a hydrogen bond donor and acceptor.
Uses
Used in Gas-phase Studies:
2,2,2-TRIFLUOROETHANOL-D3 is used as a reagent in gas-phase studies for investigating the properties and behavior of molecules in the absence of solvents. Its deuterated form provides a means to study the effects of isotopic substitution on molecular interactions and reactions.
Used in Investigating Substituent Effects in Photosolvolysis:
In the field of photochemistry, 2,2,2-TRIFLUOROETHANOL-D3 serves as a reagent to explore the impact of substituent effects on the photosolvolysis process. This application aids in understanding the role of substituents in modulating the photochemical reactions and can provide insights into the design of new photoactive compounds and materials.
While the provided materials do not explicitly mention other industries, the potential applications of 2,2,2-TRIFLUOROETHANOL-D3 could extend to various fields where its unique properties can be harnessed, such as in the development of new pharmaceuticals, materials science, or as a tool in analytical chemistry for studying molecular interactions and dynamics.
Check Digit Verification of cas no
The CAS Registry Mumber 77253-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,5 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77253-67:
(7*7)+(6*7)+(5*2)+(4*5)+(3*3)+(2*6)+(1*7)=149
149 % 10 = 9
So 77253-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C2H3F3O/c3-2(4,5)1-6/h6H,1H2/i1D2,6D
77253-67-9Relevant articles and documents
Simple and efficient catalytic reaction for the selective deuteration of alcohols
Khaskin, Eugene,Milstein, David
, p. 448 - 452 (2013/08/25)
A highly efficient system for the catalytic deuteration of α and β CH bonds of primary and secondary alcohols has been developed. The deuterium source is D2O. Together with the low catalyst loadings and the simple experimental setup, the reaction has direct application to the synthesis of bioactive isotopologues and the direct synthesis of fully deuterated substrates, such as ethanol-d6. The current system represents a significant advance in practicality for homogeneous metal catalyzed systems that carry out H/D exchange in organic substrates with water.