927804-72-6 Usage
Uses
Ethyl 3-aminofuro[2,3-c]pyridine-2-carboxylate is used as a chemical intermediate for [application reason] in [application type] due to its unique structure and potential reactivity in chemical reactions.
Used in Chemical Research:
Ethyl 3-aminofuro[2,3-c]pyridine-2-carboxylate is used as a research compound for exploring its chemical properties and potential interactions with other molecules, which could lead to new discoveries in synthetic chemistry.
Used in Pharmaceutical Development:
Ethyl 3-aminofuro[2,3-c]pyridine-2-carboxylate is used as a starting material or intermediate in the synthesis of pharmaceutical compounds, potentially contributing to the development of new drugs.
Used in Material Science:
Ethyl 3-aminofuro[2,3-c]pyridine-2-carboxylate is used as a component in the development of new materials, such as polymers or composites, where its unique structure may impart specific properties to the final product.
Note: The specific applications and reasons for use are hypothetical and would need to be confirmed through experimental studies and research.
Check Digit Verification of cas no
The CAS Registry Mumber 927804-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,7,8,0 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 927804-72:
(8*9)+(7*2)+(6*7)+(5*8)+(4*0)+(3*4)+(2*7)+(1*2)=196
196 % 10 = 6
So 927804-72-6 is a valid CAS Registry Number.
927804-72-6Relevant academic research and scientific papers
Raf inhibitor compounds and methods of use thereof
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Page/Page column 60, (2010/11/26)
Compounds of Formula I are useful for inhibiting Raf kinase and for treating disorders mediated thereby. Methods of using compounds of Formula I, and stereoisomers, geometric isomers, tautomers, solvates and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed.
Straightforward access to ethyl 3-aminofuropyridine-2-carboxylates from 1-chloro-2-cyano- or 1-hydroxy-2-cyano-substituted pyridines
Cailly, Thomas,Lemaitre, Stephane,Fabis, Frederic,Rault, Sylvain
, p. 3247 - 3251 (2008/04/03)
The conditions of the synthesis of the four regioisomers of ethyl 3-aminofuropyridine-2-carboxylate are described and discussed in detail. The starting materials are either 1-chloro-2-cyanopyridines or 1-cyano-2- hydroxypyridines. Georg Thieme Verlag Stuttgart.
