329-97-5 Usage
Uses
Used in Organic Synthesis:
Benzyltrimethylammonium fluoride is used as a reagent in organic synthesis for its ability to facilitate the introduction of fluorine atoms into organic molecules, which can significantly alter the properties and reactivity of these molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, benzyltrimethylammonium fluoride is used as a catalyst for the synthesis of various fluorine-containing compounds. The presence of fluorine in drug molecules can enhance their pharmacokinetic and pharmacodynamic properties, leading to improved therapeutic effects.
Used in Agrochemical Industry:
Benzyltrimethylammonium fluoride is also utilized in the agrochemical industry for the synthesis of fluorinated pesticides and other agrochemicals. The incorporation of fluorine can enhance the stability, selectivity, and efficacy of these compounds, making them more effective in agricultural applications.
Used in Research Laboratories:
As a source of fluoride ions, benzyltrimethylammonium fluoride is commonly used in research laboratories for various experimental purposes. Its ability to provide a controlled source of fluoride ions makes it a valuable tool in the study of fluorine chemistry and its applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 329-97-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 329-97:
(5*3)+(4*2)+(3*9)+(2*9)+(1*7)=75
75 % 10 = 5
So 329-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N.FH/c1-11(2,3)9-10-7-5-4-6-8-10;/h4-8H,9H2,1-3H3;1H/q+1;/p-1
329-97-5Relevant academic research and scientific papers
Fluoride-Mediated Reactions of Enol Silyl Ethers. Regiospecific Monoalkylation of Ketones
Kuwajima, Isao,Nakamura, Eiichi,Shimizu, Makoto
, p. 1025 - 1030 (2007/10/02)
Treatment of enol silyl ethers with alkyl halides in the presence of benzyltrimethylammonium fluoride and molecular sieves at room temperature gives the corresponding monoalkylated products with high regiospecificity.In most cases no polyalkylated products formed in the reaction.The alkylation reaction is highly chemospecific: esters, epoxides, and even ketones survive the reaction conditions.The reactions of various cyclohexanone derivatives proceed with the preferential axial attack of the electrophile.
