114643-78-6 Usage
Uses
Used in Organic Synthesis:
Pyridinium, 4-(phenylmethyl)-1-(trimethylsilyl)-, iodide is used as a catalyst or reagent in organic synthesis for its ability to facilitate various chemical reactions. Its unique structure allows it to participate in a wide range of reactions, making it a versatile tool in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Pyridinium, 4-(phenylmethyl)-1-(trimethylsilyl)-, iodide is utilized in the development of new drugs and pharmaceuticals. Its unique properties and reactivity make it a promising candidate for the synthesis of novel therapeutic agents, potentially leading to the discovery of new treatments for various diseases and conditions.
Used in Pharmaceutical Industry:
Pyridinium, 4-(phenylmethyl)-1-(trimethylsilyl)-, iodide is used as a catalyst or reagent in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its ability to facilitate various chemical reactions allows for the efficient production of APIs, contributing to the development of new and improved medications.
Overall, Pyridinium, 4-(phenylmethyl)-1-(trimethylsilyl)-, iodide has a wide range of applications in the field of chemistry and related industries, particularly in organic synthesis and medicinal chemistry. Its unique structure and reactivity make it a valuable tool for the development of new drugs and pharmaceuticals, as well as the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 114643-78-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,4 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114643-78:
(8*1)+(7*1)+(6*4)+(5*6)+(4*4)+(3*3)+(2*7)+(1*8)=116
116 % 10 = 6
So 114643-78-6 is a valid CAS Registry Number.
114643-78-6Relevant academic research and scientific papers
Syntheses with N-Trimethylsilylheteroarylium Salts: Reactions with Aldehydes, Ketones and Carboxylic Acids. Comparison of Reactivity with Analogous N-Acylheteroarylium Salts
Anders, Ernst,Stankowiak, Achim,Riemer, Roland
, p. 931 - 934 (2007/10/02)
N-Trimethylsilylheteroarylium salts 2 can be characterized as efficient silylating reagents for carbonyl compounds (5 or 8) and carbonic acids 11, their reactivity is comparable to that of N-acylheteroarylium salts 1.In some cases (depending on the nature of the substrates), their silylating power can be stronger than the acylating power of comparable salts 1.This will be demonstrated in the case of enolizable examples of 5 and 8.
