45705-36-0 Usage
Chemical Family
Pyridinium
1-Allylpyridinium belongs to the pyridinium family of compounds, which are characterized by a nitrogen-containing ring structure.
Structure
Allyl group attached to pyridine ring
The compound features an allyl group (a propene derivative) attached to a pyridine ring, which is a five-membered aromatic ring containing nitrogen.
Uses
Precursor or intermediate in synthesis
1-Allylpyridinium is commonly used as a precursor or intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties.
4. Antimicrobial properties
The compound is known to exhibit antimicrobial properties, making it a potential candidate for applications in the field of medicine.
5. Potential medical applications
Researchers are studying 1-Allylpyridinium for its potential use in medicine, particularly for its antimicrobial properties.
6. Organic synthesis building block
1-Allylpyridinium can serve as a versatile building block for the construction of more complex molecules, making it valuable in organic synthesis.
7. Hazardous chemical
It is important to handle 1-Allylpyridinium with care, as it is a hazardous chemical and can be harmful if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 45705-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,7,0 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 45705-36:
(7*4)+(6*5)+(5*7)+(4*0)+(3*5)+(2*3)+(1*6)=120
120 % 10 = 0
So 45705-36-0 is a valid CAS Registry Number.
45705-36-0Relevant articles and documents
Gas-phase ion-molecule reactions: a model for the determination of biologically reactive electrophilic contaminants in the environment.
Freeman,Johnson,Yost,Kuehl
, p. 1902 - 1910 (2007/10/02)
A promising instrumental technique has been investigated to rapidly screen complex environmental samples for chemical contaminants having the propensity to covalently bond to biomacromolecules such as DNA. Radical molecular ions of pyridine, a model compound for nucleophilic bases of DNA, were mass-selected and allowed to react with electrophilic environmental contaminants in the collision cell of a triple quadrupole mass spectrometer. Analytes were introduced into the collision cell via a gas chromatographic column. Reactive chemicals are then characterized by scanning Q3 to identify associative reaction products. A good qualitative correlation was observed for the gas-phase reactivity of a series of electrophilic reagents with both their alkylating reactivity in solution (4-(4-nitrobenzyl)pyridine) and AMES test mutagenicity which had been previously published. Femtomole limits of detection for specific associative reaction products were demonstrated. Gas-phase reactions of ions of environmental contaminants (introduced into the source) with neutral pyridine (in the collision cell) were also investigated. Reactions of the radical molecular ion of the allyl reagents with neutral pyridine were similar to results from the mass-selected reaction of the pyridine radical molecular ion with neutral allylic reagents.
