1268340-93-7 Usage
Description
(Piperidinium-1-ylmethyl)trifluoroborate is an organotrifluoroborate compound, which is a type of organoboron compound. It is characterized by its stability and versatility as a boronic acid surrogate, making it a valuable reagent in various chemical reactions and applications.
Uses
Used in Pharmaceutical Industry:
(Piperidinium-1-ylmethyl)trifluoroborate is used as a reagent in the Suzuki-Miyaura cross-coupling reaction, which is a widely employed method for the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including those found in pharmaceutical compounds.
Used in Chemical Synthesis:
(Piperidinium-1-ylmethyl)trifluoroborate is used as a versatile and stable boronic acid surrogate in cross-coupling reactions with mesylated phenol derivatives. This application is particularly useful in the synthesis of various organic compounds, such as those found in the chemical and materials science industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1268340-93-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,3,4 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1268340-93:
(9*1)+(8*2)+(7*6)+(6*8)+(5*3)+(4*4)+(3*0)+(2*9)+(1*3)=167
167 % 10 = 7
So 1268340-93-7 is a valid CAS Registry Number.
1268340-93-7Relevant articles and documents
Reinvestigation of aminomethyltrifluoroborates and their application in suzuki-miyaura cross-coupling reactions
Raushel, Jessica,Sandrock, Deidre L.,Josyula, Kanth V.,Pakyz, Deborah,Molander, Gary A.
experimental part, p. 2762 - 2769 (2011/06/17)
A reinvestigation into the chemical composition of potassium aminomethyltrifluoroborates is reported. These trifluoroborato salts have been reassigned as zwitterionic ammoniomethyltrifluoroborates. Minor adjustments to the previously disclosed reaction conditions are reported that permit a similar level of activity as nucleophiles in Suzuki-Miyaura cross-coupling reactions.
