1430722-07-8 Usage
Uses
Used in Organic Synthesis:
Potassium 3,3,3-trifluoropropane-1-trifluoroborate is used as a reagent for various organic transformations due to its stability and reactivity, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Potassium 3,3,3-trifluoropropane-1-trifluoroborate is utilized as a reagent for the synthesis of new compounds with potential biological activity, contributing to the development of novel drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, Potassium 3,3,3-trifluoropropane-1-trifluoroborate is employed for the synthesis of new compounds with potential applications in agriculture, such as pesticides and herbicides, to improve crop protection and yield.
Used in Fluorine Chemistry:
Potassium 3,3,3-trifluoropropane-1-trifluoroborate also has applications in fluorine chemistry, where it serves as a valuable tool for the synthesis of fluorinated molecules. Fluorinated compounds are important in various fields due to their unique properties, such as increased metabolic stability and lipophilicity.
Overall, Potassium 3,3,3-trifluoropropane-1-trifluoroborate is a multifaceted chemical with applications spanning across different industries, highlighting its importance in modern chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 1430722-07-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,7,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1430722-07:
(9*1)+(8*4)+(7*3)+(6*0)+(5*7)+(4*2)+(3*2)+(2*0)+(1*7)=118
118 % 10 = 8
So 1430722-07-8 is a valid CAS Registry Number.
1430722-07-8Relevant academic research and scientific papers
Ramachandran, P. Veeraraghavan,Mitsuhashi, Wataru
, p. 1252 - 1255 (2015)
A Pd-catalyzed hydrogenation of potassium (3,3,3-trifluoroprop-1-yn-1-yl)trifluoroborate providing either the (Z)- or (E)-isomer of the vinylborate in >98% purity is described. The initially formed (Z)-isomer of the alkene is transformed to the (E)-isomer with time, irrespective of the catalyst used; coupling with bromo- and iodoarenes provides a variety of (Z)- or (E)-β-trifluoromethylstyrenes. Also, a safe synthesis of the alkynyltrifluoroborate from HFC-245fa and BF3·OEt2 has been described.
