1408168-77-3 Usage
Uses
Used in Organic Synthesis:
Potassium (2-acetoxyethyl)trifluoroborate is used as a reagent in organic synthesis for the preparation of a wide range of organic compounds. Its unique structure allows it to participate in various chemical reactions, making it a valuable tool for chemists.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Potassium (2-acetoxyethyl)trifluoroborate is utilized in the synthesis of various drugs. Its ability to facilitate the formation of complex organic molecules contributes to the development of new medications and therapies.
Used in Agrochemicals:
Potassium (2-acetoxyethyl)trifluoroborate also finds application in the agrochemical sector, where it is employed in the production of pesticides, herbicides, and other agricultural chemicals. Its role in creating effective and targeted compounds supports crop protection and yield enhancement.
Used in Materials Science:
In the realm of materials science, Potassium (2-acetoxyethyl)trifluoroborate is used in the development of new materials with specific properties. Its involvement in the synthesis of advanced materials can lead to innovations in various industries, including electronics, textiles, and construction.
Check Digit Verification of cas no
The CAS Registry Mumber 1408168-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,1,6 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1408168-77:
(9*1)+(8*4)+(7*0)+(6*8)+(5*1)+(4*6)+(3*8)+(2*7)+(1*7)=163
163 % 10 = 3
So 1408168-77-3 is a valid CAS Registry Number.
1408168-77-3Relevant academic research and scientific papers
Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: Access to aryl/heteroarylethyloxy motifs
Fleury-Bregeot, Nicolas,Presset, Marc,Beaumard, Floriane,Colombel, Virginie,Oehlrich, Daniel,Rombouts, Frederik,Molander, Gary A.
, p. 10399 - 10408 (2013/01/15)
The introduction of an alkoxyethyl moiety onto aromatic substructures has remained a long-standing challenge for synthetic organic chemists. The main reasons are the inherent instability of alkoxyethylmetallic species and the lack of general procedures to access them. A new method utilizing a cross-coupling strategy based on the exceptional properties of organotrifluoroborates has been developed, and the method allows an easy and efficient installation of this unit on a broad range of aryl and heteroaryl bromides.
