54802-12-9 Usage
Description
2-(2-cyanophenoxy)acetamide is a chemical compound with the molecular formula C10H8N2O3. It is a derivative of acetamide with a cyanophenoxy group attached to the second carbon atom. 2-(2-cyanophenoxy)acetamide is commonly used as an intermediate for the synthesis of various pharmaceuticals and agrochemicals. Its potential pharmacological and biological activities make it of interest for research and development in the pharmaceutical industry. Furthermore, its chemical structure makes it suitable for use as a building block in the synthesis of other complex organic molecules.
Uses
Used in Pharmaceutical Industry:
2-(2-cyanophenoxy)acetamide is used as an intermediate for the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a key component in the development of new drugs and other therapeutic agents.
Used in Research and Development:
2-(2-cyanophenoxy)acetamide is used as a subject of research and development in the pharmaceutical industry due to its potential pharmacological and biological activities. Scientists are interested in exploring its properties and applications to create new and innovative treatments.
Used in Organic Synthesis:
2-(2-cyanophenoxy)acetamide is used as a building block in the synthesis of other complex organic molecules. Its versatile chemical structure makes it a valuable component in the creation of a wide range of organic compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 54802-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,0 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54802-12:
(7*5)+(6*4)+(5*8)+(4*0)+(3*2)+(2*1)+(1*2)=109
109 % 10 = 9
So 54802-12-9 is a valid CAS Registry Number.
54802-12-9Relevant articles and documents
The design, synthesis, and biological evaluation of PIM kinase inhibitors
Tsuhako, Amy Lew,Brown, David S.,Koltun, Elena S.,Aay, Naing,Arcalas, Arlyn,Chan, Vicky,Du, Hongwang,Engst, Stefan,Franzini, Maurizio,Galan, Adam,Huang, Ping,Johnston, Stuart,Kane, Brian,Kim, Moon H.,Douglas Laird,Lin, Rui,Mock, Lillian,Ngan, Iris,Pack, Michael,Stott, Gordon,Stout, Thomas J.,Yu, Peiwen,Zaharia, Cristiana,Zhang, Wentao,Zhou, Peiwen,Nuss, John M.,Kearney, Patrick C.,Xu, Wei
scheme or table, p. 3732 - 3738 (2012/07/17)
A series of substituted benzofuropyrimidinones with pan-PIM activities and excellent selectivity against a panel of diverse kinases is described. Initial exploration identified aryl benzofuropyrimidinones that were potent, but had cell permeability limitation. Using X-ray crystal structures of the bound PIM-1 complexes with 3, 5m, and 6d, we were able to guide the SAR and identify the alkyl benzofuropyrimidinone (6l) with good PIM potencies, permeability, and oral exposure.
HCV PROTEASE INHIBITORS
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Page/Page column 62; 64, (2011/08/04)
This invention relates to compounds of Formula (I), (II), or (III) shown in the specification. These compounds can be used to treat hepatitis C virus infection.