143924-51-0 Usage
Description
1,2,3,4,5,6-HEXAHYDRO-[2,4']BIPYRIDINYL, also known as lepidine, is a bicyclic chemical compound with the formula C10H13N. It features a 6-membered ring fused to a 4-membered ring, both containing nitrogen atoms. Lepidine is a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, and also serves as a catalyst in organic reactions. Its potential applications extend to the development of new materials, thanks to its reactivity and structural properties. As a colorless to pale yellow liquid with a characteristic odor, it requires careful handling due to potential health and environmental risks.
Uses
Used in Pharmaceutical Industry:
1,2,3,4,5,6-HEXAHYDRO-[2,4']BIPYRIDINYL is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
1,2,3,4,5,6-HEXAHYDRO-[2,4']BIPYRIDINYL is used as a component in the creation of agrochemicals, aiding in the development of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Organic Synthesis:
1,2,3,4,5,6-HEXAHYDRO-[2,4']BIPYRIDINYL is used as a catalyst in organic reactions, facilitating various chemical processes and improving the efficiency of synthesis.
Used in Material Science:
1,2,3,4,5,6-HEXAHYDRO-[2,4']BIPYRIDINYL is used in the development of new materials, leveraging its versatile reactivity and structural properties to create innovative substances with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 143924-51-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,9,2 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 143924-51:
(8*1)+(7*4)+(6*3)+(5*9)+(4*2)+(3*4)+(2*5)+(1*1)=130
130 % 10 = 0
So 143924-51-0 is a valid CAS Registry Number.
143924-51-0Relevant articles and documents
Preparation of Piperidinylpyridines via Selective Reduction of Bipyridines with Nickel-Aluminum Alloy
Lunn, George
, p. 6317 - 6320 (2007/10/02)
Bipyridines were reduced to piperidinylpyridines in modest yield using nickel-aluminum alloy in potassium hydroxide solution.The reduction was selective, and 3-substituted rings were reduced in preference to 4-substitution.Thus 2,3-bipyridine gave only 2-(3'-piperidinyl)pyridine, 2,4-bipyridine gave only 2-(4'-piperidinyl)pyridine, and 3,4-bipyridine gave only 4-(3'-piperidinyl)pyridine.The symmetrical 2,2'- and 4,4'-bipyridines also gave the corresponding piperidinylpyridines, but the reduction of 3,3'-bipyridine was too sluggish to be practical.The products were identified using 13C NMR spectroscopy, and the 13C NMR spectra of the starting bipyridines were also recorded.
