1008138-73-5 Usage
Description
5-aMino-6-Methyl-3-Pyridinecarboxylic acid ethyl ester is an organic compound characterized by the presence of a pyridine ring, which is a nitrogen-containing six-membered ring. It is also an ethyl ester and an amino acid derivative, making it a compound of interest for its potential in chemical synthesis. This molecule features an amino group (-NH2), a methyl group (-CH3), and an ethyl ester group (-COOEt) attached to different positions on the pyridine ring, hence its specific nomenclature. The exact physical and chemical properties of this compound, such as its melting point, boiling point, or toxicity, are not specified and would require experimental determination. A deeper understanding of its chemical behavior and potential applications in various fields, particularly in pharmaceuticals, would necessitate further research and contextual knowledge.
Uses
Used in Chemical Synthesis:
5-aMino-6-Methyl-3-Pyridinecarboxylic acid ethyl ester is used as a building block in chemical synthesis for its unique structural features, including the presence of an amino group, a methyl group, and an ethyl ester group. These functional groups can participate in various chemical reactions, making the compound a versatile intermediate for the synthesis of more complex organic molecules.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 5-aMino-6-Methyl-3-Pyridinecarboxylic acid ethyl ester is used as a precursor in the development of new drugs. Its structural components, including the pyridine ring and the attached functional groups, can be exploited to create molecules with specific biological activities. 5-aMino-6-Methyl-3-Pyridinecarboxylic acid ethyl ester's potential role in medicinal chemistry would be determined by its ability to interact with biological targets, such as enzymes or receptors, and its subsequent effects on physiological processes.
Used in Research and Development:
5-aMino-6-Methyl-3-Pyridinecarboxylic acid ethyl ester serves as a valuable compound in academic and industrial research settings. It can be used to explore the fundamental chemical properties of pyridine-based compounds and their reactivity in various reaction conditions. Additionally, it can be employed to study the effects of structural modifications on the compound's properties and potential applications, contributing to the advancement of organic chemistry and related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1008138-73-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,1,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1008138-73:
(9*1)+(8*0)+(7*0)+(6*8)+(5*1)+(4*3)+(3*8)+(2*7)+(1*3)=115
115 % 10 = 5
So 1008138-73-5 is a valid CAS Registry Number.
