31778-07-1 Usage
General Description
2,3-dimethylquinolizinium is a chemical compound with the molecular formula C13H15N. It belongs to the quinolizinium class of compounds and is derived from quinoline. The compound is a heterocyclic organic compound with a bicyclic structure consisting of a benzene ring fused to a pyrrolidine ring. 2,3-dimethylquinolizinium has been studied for its potential therapeutic applications, including as an anti-cancer and anti-inflammatory agent. It has also been investigated for its potential use in organic synthesis and as a versatile building block for the preparation of other novel compounds. The exact properties and potential uses of 2,3-dimethylquinolizinium continue to be explored in scientific research.
Check Digit Verification of cas no
The CAS Registry Mumber 31778-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,7 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31778-07:
(7*3)+(6*1)+(5*7)+(4*7)+(3*8)+(2*0)+(1*7)=121
121 % 10 = 1
So 31778-07-1 is a valid CAS Registry Number.
31778-07-1Relevant articles and documents
Fluorescent quinolizinium ionic liquids (salts) with unexpectedly high quantum yields up to >99%
Chen, Zhengjian,Zhang, Shiguo,Qi, Xiujuan,Liu, Shimin,Zhang, Qinghua,Deng, Youquan
, p. 8979 - 8982 (2011)
Quinolizinium ionic liquids (salts) featuring an unbranched cation core have been prepared, characterized and found to show extremely high fluorescence quantum yields in solution (Φf > 99%, λem near 334 nm) and bright cyan fluorescence in molten state (λem near 465 nm).
2-Methylpyridinium Salts as 1,4-Dinucleophiles. Quinolizinium Salts from the Westphal Condensation
Alvarez-Builla, J.,Trigo, G. Gonzales,Ezquerra, J.,Fombella, M.E.
, p. 681 - 685 (2007/10/02)
Condensation of 2-methylpyridinium salts with 1,2-dicarbonyls in the presence of base, yielded 2,3-disubstituted quinolizinium compounds.Results obtained with different pyridinium substrates are discussed.