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5-(piperidin-1-yl)quinoline is a chemical compound with the molecular formula C14H16N2. It is a derivative of quinoline, a heterocyclic aromatic compound, and features a piperidin-1-yl group attached to the 5-position of the quinoline ring. 5-(piperidin-1-yl)quinoline is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various pharmaceuticals and agrochemicals. The piperidin-1-yl group contributes to the compound's structure, potentially enhancing its biological activity and selectivity. 5-(piperidin-1-yl)quinoline is a white crystalline solid that is soluble in organic solvents and has been studied for its properties, including its reactivity and potential therapeutic uses.

1605-49-8

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1605-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1605-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1605-49:
(6*1)+(5*6)+(4*0)+(3*5)+(2*4)+(1*9)=68
68 % 10 = 8
So 1605-49-8 is a valid CAS Registry Number.

1605-49-8Downstream Products

1605-49-8Relevant academic research and scientific papers

Palladium-catalyzed microwave-assisted amination of 1-bromonaphthalenes and 5-and 8-bromoquinolines

Wang, Tammy,Magnin, David R.,Hamann, Lawrence G.

, p. 897 - 900 (2003)

1-Aminonaphthalenes and 5-and 8-aminoquinolines were rapidly prepared from the respective aryl bromides in good yields by Pd-catalyzed aryl amination under microwave conditions. Consistent improvements in yields over those obtained under standard conditions were seen with quinoline substrates. In the cases where 5-bromo-8-cyanoquinoline was used as a substrate, no desired products were obtained under standard conditions with a number of different primary and secondary amines. However, microwave conditions provided the desired products in good to excellent yields.

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