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(4-Methoxy-phenyl)-acetic acid-(2-hydroxy-ethylamide) is a complex organic compound with the molecular formula C11H15NO4. It is characterized by a 4-methoxy-phenyl group attached to an acetic acid moiety, which is further connected to a 2-hydroxy-ethylamide group. This chemical structure suggests potential applications in pharmaceuticals or as a chemical intermediate. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the methoxy group, which may affect its interaction with other molecules. Its specific uses and effects would depend on the context in which it is applied, and further research would be needed to explore its full potential.

56369-49-4

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56369-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56369-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,6 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56369-49:
(7*5)+(6*6)+(5*3)+(4*6)+(3*9)+(2*4)+(1*9)=154
154 % 10 = 4
So 56369-49-4 is a valid CAS Registry Number.

56369-49-4Relevant academic research and scientific papers

Investigation into the structure-activity relationship of novel concentration dependent, dual action T-type calcium channel agonists/antagonists

McCalmont, William F.,Patterson, Jaclyn R.,Lindenmuth, Michael A.,Heady, Tiffany N.,Haverstick, Doris M.,Gray, Lloyd S.,Macdonald, Timothy L.

, p. 3821 - 3839 (2007/10/03)

This paper describes the synthesis and biological evaluation of a series of straight chain analogs of a compound (1) that was previously synthesized in our research program. These compounds, which are T-type calcium channel antagonists, exhibits potent anti-proliferative activity against a variety of cancer cells. A structure-activity relationship of these analogs against a variety of cancer cells has provided insight into a logical pharmacophore for this series of compounds. Furthermore, this series of compounds has presented itself as a set of novel, concentration dependent, dual action agonists/antagonists for the T-type calcium channel.

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