1622923-53-8 Usage
Description
Potassium 2-isonicotinoyltrifluoroborate, a member of the potassium acyltrifluoroborates (KATs) class, is a stable trifluoroborate salt that does not undergo trimerization. It is characterized by its unique chemical structure and properties, making it a versatile compound for various applications.
Uses
Used in Pharmaceutical Industry:
Potassium 2-isonicotinoyltrifluoroborate is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique structure allows for the creation of novel molecules with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, potassium 2-isonicotinoyltrifluoroborate serves as a valuable reagent for studying the properties and reactions of trifluoroborate salts. This contributes to the advancement of knowledge in organic and inorganic chemistry.
Used in Material Science:
Potassium 2-isonicotinoyltrifluoroborate is utilized as a component in the development of new materials with specific properties, such as improved stability or reactivity. Its unique characteristics make it a promising candidate for various material science applications.
Used in Catalyst Design:
As a member of the KATs class, potassium 2-isonicotinoyltrifluoroborate is employed in the design and development of new catalysts for various chemical reactions. Its stability and reactivity make it a valuable asset in the field of catalysis.
Check Digit Verification of cas no
The CAS Registry Mumber 1622923-53-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,2,9,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1622923-53:
(9*1)+(8*6)+(7*2)+(6*2)+(5*9)+(4*2)+(3*3)+(2*5)+(1*3)=158
158 % 10 = 8
So 1622923-53-8 is a valid CAS Registry Number.
1622923-53-8Relevant articles and documents
Mechanism-Based Design of Quinoline Potassium Acyltrifluoroborates for Rapid Amide-Forming Ligations at Physiological pH
Bode, Jeffrey W.,Da Ros, Sara,Dzeng, Yi-Chung,Lam, Erwin,Tanriver, Matthias
supporting information, p. 17557 - 17565 (2021/11/04)
Potassium acyltrifluoroborates (KATs) undergo chemoselective amide-forming ligations with hydroxylamines. Under aqueous, acidic conditions these ligations can proceed rapidly, with rate constants of ～20 M-1 s-1. The requirement for lower pH to obtain the
