98195-14-3 Usage
Chemical structure
A complex chemical compound with multiple functional groups, including a benzyl group, a methyl group, a piperidine ring, two carbonitrile groups, and an undecyl group.
Benzyl group
A phenylmethyl group (C6H5-CH2-) attached to the piperidine ring.
Methyl group
A single carbon atom (-CH3) attached to the piperidine ring.
Piperidine ring
A six-membered nitrogen-containing ring that serves as the central structure of the compound.
Carbonitrile groups
Two CN groups attached to the 2 and 6 positions of the piperidine ring, contributing to the compound's reactivity.
Undecyl group
An alkyl chain consisting of eleven carbon atoms (-C11H23) attached to the piperidine ring.
Synthesis
Commonly used as a precursor in the synthesis of other complex organic compounds.
Biological activity
Exhibits biological activity, making it a potential candidate for drug development and medicinal chemistry research.
Handling
Requires careful handling due to its complex structure and multiple functional groups.
Synthesis techniques
Demands precise synthesis techniques to ensure the correct formation of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 98195-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,9 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98195-14:
(7*9)+(6*8)+(5*1)+(4*9)+(3*5)+(2*1)+(1*4)=173
173 % 10 = 3
So 98195-14-3 is a valid CAS Registry Number.
98195-14-3Relevant academic research and scientific papers
Efficient and Convenient Method for Synthesis of Solenopsin A and Its Analogues Using 1-Benzyl-2,6-dicyanopiperidine
Takahashi, Kazumasa,Kurita, Hideki,Ogura, Katsuyuki,Iida, Hirotada
, p. 4368 - 4371 (2007/10/02)
An efficient synthetic sequence proposed here provides a new method for preparation of not only solenopsin A, i.e., trans-2-methyl-6-undecylpiperidine, but also coniine, i.e., 2-propylpiperidine, and other 2,6-dialkylpiperidine alkaloids: A reaction of 1-benzyl-2,6-dicyanopiperidine (1) with alkyl halides selectively gives 2-alkyl- and 2,6-dialkyl-1-benzyl-2,6-dicyanopiperidines (2 and 3), decyanation of which affords respectively 2-alkyl- and 2,6-dialkyl-1-benzylpiperidines (4 and 5) in high yields.
