2436-92-2 Usage
Uses
Used in Pharmaceutical Industry:
3,4-Dimethylquinoline is used as a building block for the synthesis of various pharmaceuticals due to its ability to be incorporated into complex organic molecules, contributing to the development of new drugs with potential therapeutic applications.
Used in Dye Industry:
In the dye industry, 3,4-dimethylquinoline is utilized as a precursor in the production of dyes, where its chemical properties allow for the creation of a wide range of colorants used in various applications, including textiles and printing.
Used in Chemical Industry:
3,4-Dimethylquinoline serves as an intermediate in the manufacture of rubber chemicals, playing a crucial role in the production of additives that enhance the performance and longevity of rubber products.
Used as a Corrosion Inhibitor:
3,4-Dimethylquinoline is employed as a corrosion inhibitor, leveraging its chemical properties to protect metal surfaces from degradation in various industrial applications, thereby extending the service life of equipment and infrastructure.
Check Digit Verification of cas no
The CAS Registry Mumber 2436-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2436-92:
(6*2)+(5*4)+(4*3)+(3*6)+(2*9)+(1*2)=82
82 % 10 = 2
So 2436-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N/c1-8-7-12-11-6-4-3-5-10(11)9(8)2/h3-7H,1-2H3
2436-92-2Relevant academic research and scientific papers
Addition of propargyltrimethylsilane to N-methyleneamine equivalents: Generation and electrophilic cyclization of vinylic carbocations
Ha, Hyun-Joon,Lee, Young-Scong,Ahn, Young-Gil
, p. 2357 - 2364 (2007/10/03)
Lewis acid induced N-methyleneamine equivalents from N-(methoxymethyl)anilines or 1,3,5-triphenylhexahydro-1,3,5-triazines reacted with propargyltrimethylsilanes to give N-buta-2,3-dienylanilines, 4-methylene-1,2,3,4-tetrahydroquinolines and its oxidized product of 4-methylquinolines. These products came from branching reactions of the elimination and electrophilic aromatic substitution from the same vinylic carbocation intermediate.
