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5-(p-tolylamino)pentan-2-one is an organic compound with the molecular formula C12H19NO. It is a derivative of pentan-2-one, featuring a p-tolylamine group attached to the fifth carbon atom. 5-(p-tolylamino)pentan-2-one is characterized by its amine functional group, which is derived from p-tolylamine, and a ketone group at the second carbon position. It is a colorless liquid with a distinct amine-like odor and is soluble in organic solvents. The compound has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is important to handle 5-(p-tolylamino)pentan-2-one with care, as it may have potential health risks and should be used in accordance with proper safety protocols.

6724-70-5

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6724-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6724-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,2 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6724-70:
(6*6)+(5*7)+(4*2)+(3*4)+(2*7)+(1*0)=105
105 % 10 = 5
So 6724-70-5 is a valid CAS Registry Number.

6724-70-5Downstream Products

6724-70-5Relevant academic research and scientific papers

SnCl4 mediated synthesis of γ-amino ketones derivatives via the ring-opening reaction of 4,5-dihydropyrroles

Zhang, Zhiguo,Wang, Dan,Wang, Bing,Liu, Qingfeng,Liu, Tongxin,Zhang, Wei,Yuan, Beibei,Zhao, Zhijia,Han, Dandan,Zhang, Guisheng

, p. 9063 - 9067 (2013/09/24)

This paper presents an alternative route to γ-amino ketones via a SnCl4·5H2O mediated ring-opening reaction of the 4,5-dihydropyrroles with the advantages of readily available reactants, good to excellent yields and applicability to a wide range of substrates.

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