107658-27-5 Usage
Description
3-Pyridyl Trifluoromethanesulfonate, with the CAS number 107658-27-5, is a light yellow oil compound that is primarily utilized in the field of organic synthesis. It is known for its unique chemical properties that make it a valuable component in various chemical reactions and processes.
Uses
Used in Organic Synthesis:
3-Pyridyl Trifluoromethanesulfonate is used as a reagent in organic synthesis for its ability to facilitate a range of chemical reactions. Its light yellow oil form allows for easy handling and integration into various processes, making it a versatile compound for use in the creation of new molecules and compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Pyridyl Trifluoromethanesulfonate is used as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique chemical properties enable the development of new drugs with improved efficacy and reduced side effects, contributing to the advancement of medical treatments.
Used in Chemical Research:
3-Pyridyl Trifluoromethanesulfonate is also employed in chemical research as a tool to study and understand the behavior of different chemical reactions. Its use in research helps scientists gain insights into the mechanisms of various chemical processes, leading to the development of new methodologies and techniques in the field of chemistry.
Used in Material Science:
In the field of material science, 3-Pyridyl Trifluoromethanesulfonate is used as a component in the development of new materials with specific properties. Its unique chemical characteristics allow for the creation of materials with enhanced performance, such as improved stability, reactivity, or selectivity, which can be applied in various industries, including electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 107658-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,5 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107658-27:
(8*1)+(7*0)+(6*7)+(5*6)+(4*5)+(3*8)+(2*2)+(1*7)=135
135 % 10 = 5
So 107658-27-5 is a valid CAS Registry Number.
107658-27-5Relevant articles and documents
A soluble polymer-supported triflating reagent: a high-throughput synthetic approach to aryl and enol triflates.
Wentworth,Wentworth Jr.,Mansoor,Janda
, p. 477 - 480 (2000)
[reaction: see text] The high-yielding synthesis and application of the first example of a polymer-supported reagent for the preparation of trifluoromethanesulfonates (triflates) is described. This new reagent efficiently triflates aryl alcohols and lithi
Palladium Catalysed Alkoxycarbonylation of Phenols to Benzoate Esters
Dolle, Roland E.,Schmidt, Stanley J.,Kruse, Lawrence I.
, p. 904 - 905 (1987)
The methoxycarbonylation of aryl trifluoromethanesulphonates with CO and aliphatic alcohols is catalysed by Pd(OAc)2-1,3-bis(diphenylphosphino)propane in high yield at 70 deg C and ambient CO pressure.
Solvent-free ruthenium-catalysed triflate coupling as a convenient method for selective azole-o-C-H monoarylation
Abidi, Oumaima,Boubaker, Taoufik,Hierso, Jean-Cyrille,Roger, Julien
supporting information, p. 5916 - 5919 (2019/06/24)
Metal-catalysed ortho-directed C-H functionalization usually faces selectivity issues in the competition between mono- and disubstitution processes. We report herein the ruthenium-catalysed N-directed C-H monoarylation of arylpyrazoles with a selectivity
Pd-Catalyzed Conjunctive Cross-Coupling between Grignard-Derived Boron “Ate” Complexes and C(sp2) Halides or Triflates: NaOTf as a Grignard Activator and Halide Scavenger
Lovinger, Gabriel J.,Aparece, Mark D.,Morken, James P.
supporting information, p. 3153 - 3160 (2017/03/11)
Catalytic enantioselective conjunctive cross-couplings that employ Grignard reagents are shown to furnish an array of nonracemic chiral organoboronic esters in an efficient and highly selective fashion. The utility of sodium triflate in facilitating this reaction is two-fold: it enables “ate” complex formation and overcomes catalytic inhibition by halide ions.