855292-39-6 Usage
Uses
Used in Medicinal Chemistry:
2-(ISOQUINOLIN-1-YL)ACETIC ACID is used as a ligand for metal complexes, which is crucial for the development of new antitumor agents. Its unique structure allows it to form stable complexes with metals, enhancing the therapeutic potential of these agents.
Used in Organic Synthesis:
2-(ISOQUINOLIN-1-YL)ACETIC ACID is used as a building block in the synthesis of other organic compounds. Its versatile structure enables the creation of a wide range of molecules with diverse properties and applications.
Used in Heterocyclic Chemistry:
2-(ISOQUINOLIN-1-YL)ACETIC ACID is used as a key component in the creation of heterocyclic molecules. Its ability to form heterocyclic rings with various functional groups makes it a valuable asset in the development of novel compounds with potential applications in pharmaceuticals, materials science, and other areas.
Used in Research and Development:
2-(ISOQUINOLIN-1-YL)ACETIC ACID is used as a subject of study in research and development efforts aimed at understanding its properties, reactivity, and potential applications. Its unique structure and potential as a ligand for metal complexes make it an attractive candidate for further investigation and exploration of its capabilities in various scientific and technological domains.
Check Digit Verification of cas no
The CAS Registry Mumber 855292-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,2,9 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 855292-39:
(8*8)+(7*5)+(6*5)+(5*2)+(4*9)+(3*2)+(2*3)+(1*9)=196
196 % 10 = 6
So 855292-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c13-11(14)7-10-9-4-2-1-3-8(9)5-6-12-10/h1-6H,7H2,(H,13,14)
855292-39-6Relevant academic research and scientific papers
Synthesis, anticonvulsant activity, and neuropathic pain-attenuating activity of N-benzyl 2-amino-2-(hetero)aromatic acetamides
Baruah, Pranjal K.,Dinsmore, Jason,King, Amber M.,Salomé, Christophe,De Ryck, Marc,Kaminski, Rafal,Provins, Laurent,Kohn, Harold
supporting information; experimental part, p. 3551 - 3564 (2012/07/28)
N-Benzyl 2-acetamido-2-substituted acetamides, where the 2-substituent is a (hetero)aromatic moiety, are potent anticonvulsants. We report the synthesis and whole animal pharmacological evaluation of 16 analogues where the terminal 2-acetyl group was removed to give the corresponding primary amino acid derivatives (PAADs). Conversion to the PAAD structure led to a substantial drop in seizure protection in animal tests, demonstrating the importance of the N-acetyl moiety for anticonvulsant activity. However, several of the PAADs displayed notable pain-attenuating activities in a mouse model.
