114643-78-6 Usage
General Description
Pyridinium, 4-(phenylmethyl)-1-(trimethylsilyl)-, iodide is a chemical compound that belongs to the class of pyridinium salts. It is made up of a pyridinium cation with a phenylmethyl and trimethylsilyl group attached, along with an iodide anion. Pyridinium, 4-(phenylmethyl)-1-(trimethylsilyl)-, iodide is often used in organic synthesis as a catalyst or reagent due to its ability to facilitate various chemical reactions. It can also be utilized in medicinal chemistry, specifically in the development of new drugs and pharmaceuticals. Overall, Pyridinium, 4-(phenylmethyl)-1-(trimethylsilyl)-, iodide has versatile applications in the field of chemistry and related industries.
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 articles and documents
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.
