106006-86-4 Usage
Description
CIS-1-BENZYL-2,6-DICYANOPIPERIDINE is a chemical compound belonging to the class of organic compounds known as dicyanopyridines. It features a piperidine ring with two cyanide groups and a benzyl group in the cis position relative to the cyano groups. This white to off-white solid is sparingly soluble in water but more soluble in organic solvents. Due to its moderate to high acute toxicity, appropriate handling and safety precautions are necessary when working with this compound.
Uses
Used in Pharmaceutical Synthesis:
CIS-1-BENZYL-2,6-DICYANOPIPERIDINE is used as an intermediate in the synthesis of pharmaceutical drugs. Its unique structure and properties make it a valuable component in the development of new medications.
Used in Agrochemical Production:
CIS-1-BENZYL-2,6-DICYANOPIPERIDINE is also utilized in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Materials Science:
CIS-1-BENZYL-2,6-DICYANOPIPERIDINE has potential applications in materials science, where its properties can be harnessed to create novel materials with specific characteristics for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 106006-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,0 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106006-86:
(8*1)+(7*0)+(6*6)+(5*0)+(4*0)+(3*6)+(2*8)+(1*6)=84
84 % 10 = 4
So 106006-86-4 is a valid CAS Registry Number.
106006-86-4Relevant articles and documents
Total synthesis of (-)-Lycoperine a
Rychnovsky, Scott D.,Nakamura, Yoshitaka,Burke, Anthony M.,Kotani, Shunsuke,Ziller, Joseph W.
supporting information; experimental part, p. 72 - 75 (2010/03/03)
Chemical Equation Presented Lycoperine A was synthesized through a highly convergent route in which a double alkylation of 2,6-dicyano-N-benzylpiperidine with the octahydroquinoline moiety gave the lycoperine skeleton. The octahydroquinoline was prepared by a desymmetrization reaction of 5-methylcyclohexane-1,3-dione. Hydrolysis, reductive amination, and cyclization gave lycoperine A in 13 steps and 3% overall yield. The absolute configuration of lycoperine A was assigned as 6R,6′R,8′,R,13S,17R.
Stereoselctive Synthesis of 1-Substituted 2,6-Dicyanopiperidines and Transformation of 2,6-Dialkylated Products of 1-Phenyl-2,6-dicyanopiperidine to δ-Diketones and Cyclohexenones
Takahashi, Kazumasa,Mikajiri, Tsutomu,Kurita, Hideki,Ogura, Katsuyuki,Iida, Hirotada
, p. 4372 - 4375 (2007/10/02)
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