77253-67-9

Usage

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.

InChI:InChI=1/C2H3F3O/c3-2(4,5)1-6/h6H,1H2/i1D2,6D

Upstream product

• 407-25-0 trifluoroacetic anhydride 
• 75-89-8 2,2,2-trifluoroethanol 

Downstream Products

• 7448-86-4 1-(4-methoxyphenyl)prop-2-en-1-one 
• 18293-99-7 Prenyltrimethylsilane 
• 18294-00-3 trimethyl-(3-methyl-but-3-enyl)-silane 
• 74-85-1 ethene 
• 6755-54-0 ethylene-1,1-d2 
• 815574-19-7 (C₆H₃(CH₃)2NC(CH₃))2Pt(C₆H₃(CH₃)2)(CF₃C⁽²⁾H₂O⁽²⁾H)⁽¹⁺⁾*CF₃C⁽²⁾H₂OB(C₆F₅)3^(1-)=(C₁₀H₁₂N)2PtC₈H₉(CF₃C⁽²⁾H₂O)2⁽²⁾HB(C₆F₅)3 
• 815574-17-5 (C₆H₃(CH₃)2NC(CH₃))2Pt(CH₂C₆H₃(CH₃)2)(CF₃C⁽²⁾H₂O⁽²⁾H)⁽¹⁺⁾*CF₃C⁽²⁾H₂OB(C₆F₅)3^(1-)=C₂₉H₃₅N₂Pt(CF₃C⁽²⁾H₂O)2⁽²⁾HB(C₆F₅)3 
• 815574-25-5 [Pt(CH₂D)(N(3,5-Me₂C₆H₃)CMe)2(trifluoroethanol-d3)][CF₃C⁽²⁾H₂OB(C₆F₅)3] 
• 862606-12-0 [((3,5-t-Bu₂C₆H₃)N=C(Me)C(Me)=N(3,5-t-Bu₂C₆H₃))Pt)(1,4-diethylbenzene(-1H))]⁽¹⁺⁾ 
• 923603-30-9 [((C(CH₃)N(C₆H₂(CH₃)3))2)Pt(Me)(1-methylindole-d1)]⁽¹⁺⁾ 

Relevant academic research and scientific papers

Simple and efficient catalytic reaction for the selective deuteration of alcohols

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.

METHOD FOR PRODUCING DEUTERATED PERFLUOROALYKYL METHANOL

PROBLEM TO BE SOLVED: To provide a method for safely and efficiently producing a deuterated perfluoroalykyl methanol. SOLUTION: This method for producing the deuterated perfluoroalykyl methanol expressed by general formula (I): RfCD2O-A (Rf is a perfluoroalkyl; and A is D or H) comprises reducing an perfluorcarboxylic acid anhydride expressed by general formula (II): (RfCO)2O by using deuterium in the presence of a transition metal catalyst.