4329-72-0 Usage
Description
1-(4-nitrobenzyl)pyridinium is a chemical compound that features a pyridine ring with a 4-nitrobenzyl group attached to it. 1-(4-nitrobenzyl)pyridinium is recognized for its role as a building block in organic synthesis, allowing for the creation of various derivatives with distinct properties and functions. Additionally, it has garnered interest due to its potential as a neurotransmitter in the brain and its possible effects on the central nervous system. It is crucial to handle this compound with caution, as it may possess hazardous properties and should be utilized by trained professionals in a controlled setting.
Uses
Used in Organic Synthesis:
1-(4-nitrobenzyl)pyridinium is used as a building block for [creating a variety of derivatives with different properties and functions] because of its versatile chemical structure that allows for further modification and synthesis of new compounds.
Used in Pharmaceutical Research:
1-(4-nitrobenzyl)pyridinium is used as a potential neurotransmitter for [exploring its effects on the central nervous system] due to its structural similarity to certain neurotransmitters and its potential interactions with neurological receptors.
Used in Chemical Compound Development:
1-(4-nitrobenzyl)pyridinium is used as a starting material for [developing new chemical compounds] in various industries, such as pharmaceuticals, agrochemicals, and materials science, thanks to its reactivity and the possibility of creating diverse derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 4329-72-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4329-72:
(6*4)+(5*3)+(4*2)+(3*9)+(2*7)+(1*2)=90
90 % 10 = 0
So 4329-72-0 is a valid CAS Registry Number.
4329-72-0Relevant articles and documents
Internal energy deposition for low energy, femtosecond laser vaporization and nanospray post-ionization mass spectrometry using thermometer ions
Flanigan, Paul M.,Shi, Fengjian,Archer, Jieutonne J.,Levis, Robert J.
, p. 716 - 724 (2015/05/05)
The internal energy of p-substituted benzylpyridinium ions after laser vaporization using low energy, femtosecond duration laser pulses of wavelengths 800 and 1042 nm was determined using the survival yield method. Laser vaporization of dried benzylpyridi
Surface acoustic wave nebulization produces ions with lower internal energy than electrospray ionization
Huang, Yue,Turecek, Frantisek,Yoon, Sung Hwan,Heron, Scott R.,Masselon, Christophe D.,Edgar, J. Scott,Goodlett, David R.
, p. 1062 - 1070,9 (2020/08/24)
Surface acoustic wave nebulization (SAWN) has recently been reported as a novel method to transfer non-volatile analytes directly from solution to the gas phase for mass spectrometric analysis. Here we present a comparison of the survival yield of SAWN ve
Conformational investigation of N-aralkylpyridinium ions by Cotton-Mouton effect method
Bulgarevich, S. B.,Bren, D. V.,Movshovic, D. Y.,Finocchiaro, P.,Failla, S.
, p. 147 - 156 (2007/10/02)
Molar Cotton-Mouton constants and refractions are reported at 298 K for the following N-aralkylpyridinium cations as solutes in water or acetonitrile: (C6H5)CH2(+NC5H5), (4-ClC6H4)CH2(+NC5H5), (3-ClC6H4)CH2(+NC5H5), (3-ClC
