1268340-94-8 Usage
Uses
Used in Pharmaceutical Industry:
(MorpholiniuM-4-ylMethyl)trifluoroborate internal salt, 95% is used as a synthetic intermediate for the development of new pharmaceuticals. Its reactivity and versatility in chemical reactions allow for the creation of a wide range of drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
(MorpholiniuM-4-ylMethyl)trifluoroborate internal salt, 95% is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique chemical properties enable the development of novel compounds with improved efficacy and selectivity in controlling pests and weeds.
Used in Materials Science:
(MorpholiniuM-4-ylMethyl)trifluoroborate internal salt, 95% is used as a key component in the development of advanced materials with specific properties, such as improved conductivity, strength, or stability. Its incorporation into various materials can lead to enhanced performance and new applications in fields like electronics, energy storage, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 1268340-94-8 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 1268340-94:
(9*1)+(8*2)+(7*6)+(6*8)+(5*3)+(4*4)+(3*0)+(2*9)+(1*4)=168
168 % 10 = 8
So 1268340-94-8 is a valid CAS Registry Number.
1268340-94-8Relevant academic research and scientific papers
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.
