6192-95-6 Usage
Uses
Used in Organic Synthesis:
(1-benzyl-2-methyl-6-phenylpyridin-4(1H)-ylidene)propanedinitrile is used as a reactive intermediate for the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable building block in the creation of new molecules with specific properties.
Used in Medicinal Chemistry:
In the pharmaceutical industry, (1-benzyl-2-methyl-6-phenylpyridin-4(1H)-ylidene)propanedinitrile is used as a potential lead compound for the development of new drugs. The presence of the benzyl and methyl groups suggests that it may interact with biological targets in ways that could be harnessed for therapeutic purposes.
Used in Research and Development:
Due to its complex structure and potential reactivity, (1-benzyl-2-methyl-6-phenylpyridin-4(1H)-ylidene)propanedinitrile is used in research settings to explore its chemical properties and potential applications. It serves as a subject of study for understanding the behavior of similar compounds and their interactions with biological systems.
Caution:
Given the complexity and potential reactivity of (1-benzyl-2-methyl-6-phenylpyridin-4(1H)-ylidene)propanedinitrile, it is essential to exercise caution when handling and using (1-benzyl-2-methyl-6-phenylpyridin-4(1H)-ylidene)propanedinitrile in a laboratory setting. Proper safety measures should be taken to ensure the well-being of researchers and the integrity of experiments.
Check Digit Verification of cas no
The CAS Registry Mumber 6192-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6192-95:
(6*6)+(5*1)+(4*9)+(3*2)+(2*9)+(1*5)=106
106 % 10 = 6
So 6192-95-6 is a valid CAS Registry Number.
6192-95-6Relevant academic research and scientific papers
PROCESS FOR PREPARING BENZYLATED AMINES
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Page/Page column 8, (2008/06/13)
This present invention relates to a process for preparing benzylated amines by the reaction of an amine selected from methamphetamine and propylhexedrine with benzyl halide. Numerous improvements are obtained by employing the amine in molar excess with respect to benzyl halide, preferably in a molar ratio of 2 to 1. The excess amine is employed to selectively neutralize by-product acid as the amine salt. The amine salt is then separated from the reaction mixture and basified to reclaim starting amine for recycle to the process.
