848347-44-4 Usage
Uses
Used in Organic Synthesis:
Pentafluorophenyl nicotinate is utilized as a reagent in esterification reactions, contributing to the formation of esters which are essential in the synthesis of various organic compounds.
Used in Pharmaceutical Production:
It serves as a building block in the production of pharmaceuticals, playing a pivotal role in the creation of new drugs and medicinal compounds due to its unique structure and reactivity.
Used in Agrochemical Production:
Pentafluorophenyl nicotinate is also employed in the synthesis of agrochemicals, which are vital for the development of pesticides and other agricultural products to enhance crop protection and yield.
Used in Drug Delivery Systems:
Pentafluorophenyl nicotinate has been studied for its potential as a drug delivery system, leveraging its unique chemical properties to improve the efficacy and targeted delivery of pharmaceutical agents.
Used in Chemical Research:
Due to its high reactivity and fluorination, Pentafluorophenyl nicotinate is valuable in chemical research for exploring new reaction pathways and developing innovative synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 848347-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,3,4 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 848347-44:
(8*8)+(7*4)+(6*8)+(5*3)+(4*4)+(3*7)+(2*4)+(1*4)=204
204 % 10 = 4
So 848347-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H4F5NO2/c13-6-7(14)9(16)11(10(17)8(6)15)20-12(19)5-2-1-3-18-4-5/h1-4H
848347-44-4Relevant academic research and scientific papers
Babadzhanova,Kirij,Yagupolskii,Tyrra,Naumann
, p. 1813 - 1819 (2005)
A new convenient synthetic procedure to obtain various 1,1,1,3,3,3- hexafluoro-2-organyl-propan-2-ols and the corresponding trimethylsilyl ethers has been worked out starting from anhydrides or activated esters of carboxylic acids and trimethyl(trifluoromethyl)silane in the presence of tetramethylammonium fluoride. Conditions for the selective formation of 1,1,1,3,3,3-hexafluoro-2-organyl-propan-2-ols as well as the trimethylsilyl derivatives have been found.
