90670-03-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
1,4'-Bipiperidine, 1'-benzoylis derived from piperidine, which is a heterocyclic amine compound consisting of a six-membered ring.
Explanation
The benzoyl group (C6H5CO-) is attached to the piperidine ring, giving the compound its unique chemical properties.
Explanation
The compound is commonly used in research related to the development of new drugs and medication due to its unique chemical properties.
Explanation
1,4'-Bipiperidine, 1'-benzoylis known for its potential as a building block in the synthesis of complex organic molecules, which can be used in various applications.
Explanation
While the compound may have potential medicinal uses, further research and studies are needed to fully understand its properties and potential benefits.
Explanation
More research is needed to fully comprehend the compound's properties, potential applications, and benefits in the field of chemistry and pharmaceuticals.
Derivative of Piperidine
Heterocyclic amine compound with a six-membered ring
Chemical Structure
Contains a benzoyl group attached to the piperidine ring
Applications
Chemical and pharmaceutical research
Building Block
Synthesis of complex organic molecules
Potential Medicinal Uses
Unknown at this time
Further Research
Required to understand properties and benefits
Check Digit Verification of cas no
The CAS Registry Mumber 90670-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,7 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90670-03:
(7*9)+(6*0)+(5*6)+(4*7)+(3*0)+(2*0)+(1*3)=124
124 % 10 = 4
So 90670-03-4 is a valid CAS Registry Number.
90670-03-4Relevant academic research and scientific papers
Olofson, R. A.,Abbott, Duain E.
, p. 2795 - 2799 (1984)
Primary alkyl chlorides (R-Cl) are easily isolated in excellent yield after treatment of the appropriate N-alkylpiperidines (R-NC5H10) with α-chloroethyl chloroformate.The method is exemplified by the conversion of a variety of alkylpiperidines, including systems with other sensitive functionalities, to the respective chlorides in yields varying from 90 to 97percent.The potential significance of this process in drug congener preparation and in total synthesis is outlined.Similar fragmentations of N-sec-alkylpiperidines are described.
