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6-oxo-3-phenyl-piperidine-3-carboxylic acid ethyl ester is a complex organic compound with the molecular formula C15H17NO3. It is a derivative of piperidine, a heterocyclic amine, and features a phenyl group attached to the 3-position, an ester group at the 3-carboxylic acid position, and an ethyl ester group. 6-oxo-3-phenyl-piperidine-3-carboxylic acid ethyl ester is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure. It is typically synthesized through various chemical reactions and can be used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its reactivity and stability, make it a valuable building block in organic chemistry and drug development.

5632-70-2

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5632-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5632-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5632-70:
(6*5)+(5*6)+(4*3)+(3*2)+(2*7)+(1*0)=92
92 % 10 = 2
So 5632-70-2 is a valid CAS Registry Number.

5632-70-2Relevant academic research and scientific papers

Development of a novel tricyclic class of potent and selective FIXa inhibitors

Meng, Dongfang,Andre, Patrick,Bateman, Thomas J.,Berger, Richard,Chen, Yi-Heng,Desai, Kunal,Dewnani, Sunita,Ellsworth, Kenneth,Feng, Daming,Geissler, Wayne M.,Guo, Liangqin,Hruza, Alan,Jian, Tianying,Li, Hong,Metzger, Joe,Parker, Dann L.,Reichert, Paul,Sherer, Edward C.,Smith, Cameron J.,Sonatore, Lisa M.,Tschirret-Guth, Richard,Wu, Jane,Xu, Jiayi,Zhang, Ting,Campeau, Louis-Charles,Orr, Robert,Poirier, Marc,McCabe-Dunn, Jamie,Araki, Kazuto,Nishimura, Teruyuki,Sakurada, Isao,Hirabayashi, Tomokazu,Wood, Harold B.

, p. 5437 - 5443 (2015/11/09)

Using structure based drug design, a novel class of potent coagulation factor IXa (FIXa) inhibitors was designed and synthesized. High selectivity over FXa inhibition was achieved. Selected compounds were evaluated in rat IV/PO pharmacokinetic (PK) studies and demonstrated desirable oral PK profiles. Finally, the pharmacodynamics (PD) of this class of molecules were evaluated in thrombin generation assay (TGA) in Corn Trypsin Inhibitor (CTI) citrated human plasma and demonstrated characteristics of a FIXa inhibitor.

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