66193-87-1 Usage
Description
2-aMino-1,2-dihydroisoquinolin-1(2H)-one, also known as ADQC, is a heterocyclic chemical compound with the molecular formula C9H10N2O. It features an isoquinoline ring system and an amino group, and has been studied for its potential pharmacological properties, such as anti-cancer, anti-inflammatory, and monoamine oxidase inhibitory activities. This makes ADQC a promising candidate for the development of drugs to treat various conditions, including neurodegenerative diseases like Parkinson's and Alzheimer's.
Uses
Used in Pharmaceutical Industry:
2-aMino-1,2-dihydroisoquinolin-1(2H)-one is used as a potential drug candidate for its anti-cancer properties, targeting various types of cancer by inhibiting key pathways and processes that contribute to tumor growth and progression.
2-aMino-1,2-dihydroisoquinolin-1(2H)-one is also used as an anti-inflammatory agent, helping to reduce inflammation and associated symptoms in various conditions.
Furthermore, 2-aMino-1,2-dihydroisoquinolin-1(2H)-one is used as a monoamine oxidase inhibitor, which may make it useful in the treatment of neurodegenerative diseases such as Parkinson's and Alzheimer's by potentially slowing down the progression of these diseases and improving the quality of life for patients.
Research into the synthesis and medicinal applications of ADQC is ongoing, with the aim of developing it into an effective and safe drug for various therapeutic purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 66193-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,9 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66193-87:
(7*6)+(6*6)+(5*1)+(4*9)+(3*3)+(2*8)+(1*7)=151
151 % 10 = 1
So 66193-87-1 is a valid CAS Registry Number.
66193-87-1Relevant articles and documents
Selective Dimerizations of Substituted N-Aminopyridinium Salts and Their Benzologues
Batori, S.,Hajos, G.,Sandor P.,Messmer, A.
, p. 3062 - 3068 (2007/10/02)
N-Aminopyridinium salts bearing ester, aroyl, and cyano functions in position 2 as well as their differently annelated benzologues were reacted with hydroxide ion and alkoxides.In the case of ester compounds 1, 3, and 5, transesterification and dimerization reactions were found.Keto salts 7, 13, and 15 showed dimerization reactions coupled with methanolysis.Monocyclic cyano salt 17 gave amino-as-triazinium double salt 20 while the benzologues (21 and 27) showed three different reactions depending on the conditions used: (a) removal of the cyano group (formation of 22 and 28), (b) formation of new fused 1,2,4-triazole derivatives (26 and 29), and (c) formation of tetrazine-fused dimers (24 and 30).All N-amino-3-substituted-isoquinolinium salts (32) resulted in dimerizations retaining the 3-substituent.Comparison of these results showed that reactivity of the N-amino compound is mainly influenced by the nature of the substituents and by the relative position of the fused benzene ring with respect to the N-amino function.
