30125-77-0 Usage
Molecular structure
A unique structure consisting of a pyrroloquinoline ring system.
Type of compound
A heterocyclic compound.
Pharmacological properties
Has potential anti-inflammatory and anticancer activities.
Therapeutic potential
Has been studied as a therapeutic agent.
Biological effects
Being investigated for its effects on various biological processes.
Aromatic ring system
The compound has an aromatic ring system which contributes to its versatility.
Heteroatoms
The presence of heteroatoms makes the compound a versatile molecule for further exploration and development.
Applications in fields of medicinal chemistry and drug discovery
The compound has potential for further exploration and development in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 30125-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,2 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30125-77:
(7*3)+(6*0)+(5*1)+(4*2)+(3*5)+(2*7)+(1*7)=70
70 % 10 = 0
So 30125-77-0 is a valid CAS Registry Number.
30125-77-0Relevant academic research and scientific papers
A facile synthesis of novel pyrrolo[3,4-b]quinolin-1-one derivatives
Li, Kai,Fu, Xinbo,Zhao, Yanan,Gao, Wentao,Li, Yang
, p. 4273 - 4287 (2016/07/06)
A simple and concise construction of a series of new quinoline-based isoindolin-l-ones, namely N-substituted-2,3-dihydro-1H-pyrrolo[3,4-b]quinolin-1-ones, wherein the benzene moiety of isoindolin-l-one is replaced by a quinoline ring has been achieved via
Total synthesis of structures proposed for quinocitrinines A and B and their analogs. Microwave energy as efficient tool for generating heterocycles
Machtey, Victoria,Gottlieb, Hugo E.,Byk, Gerardo
experimental part, p. 308 - 324 (2011/08/22)
A first total synthesis of the structures proposed for quinocitrinines A and B has been accomplished by a three steps strategy which also applies for the synthesis of non-natural analogs. In the first step a microwave assisted Friedlander condensation bet
