188825-10-7 Usage
Description
2H,6H-Oxazolo[5,4,3-ij]quinolin-2-one, 6-(2-aminophenyl)-7-hydroxy-8,9-bis(1-methylethoxy)is a complex organic compound characterized by a fused oxazole and quinolinone ring system. It features an aminophenyl group at the 6th position, a hydroxy group at the 7th position, and two 1-methylethoxy groups at the 8th and 9th positions of the quinolinone ring. 2H,6H-Oxazolo[5,4,3-ij]quinolin-2-one, 6-(2-aminophenyl)-7-hydroxy-8,9-bis(1-methylethoxy)has potential biological and pharmacological activities and may be utilized as a pharmaceutical intermediate or in research applications. Further investigation and testing are required to determine its specific properties and uses.
Uses
Used in Pharmaceutical Industry:
2H,6H-Oxazolo[5,4,3-ij]quinolin-2-one, 6-(2-aminophenyl)-7-hydroxy-8,9-bis(1-methylethoxy)is used as a pharmaceutical intermediate for the development of new drugs due to its potential biological and pharmacological activities.
Used in Research Applications:
2H,6H-Oxazolo[5,4,3-ij]quinolin-2-one, 6-(2-aminophenyl)-7-hydroxy-8,9-bis(1-methylethoxy)is utilized in research settings to explore its potential applications in the field of medicine and pharmacology, as well as to understand its chemical properties and interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 188825-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,8,2 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 188825-10:
(8*1)+(7*8)+(6*8)+(5*8)+(4*2)+(3*5)+(2*1)+(1*0)=177
177 % 10 = 7
So 188825-10-7 is a valid CAS Registry Number.
188825-10-7Relevant articles and documents
Versatile Synthesis of Dihydroquinolines and Quinoline Quinones Using Cyclobutenediones. Construction of the Pyridoacridine Ring System
Zhang, Dawei,Llorente, Isidro,Liebeskind, Lanny S.
, p. 4330 - 4338 (2007/10/03)
1-BOC-2-lithio-1, 4-dihydropyridines were condensed with 3,4-disubstituted cyclobutenediones to produce 1,2-adducts. Neat thermolysis under oxygen-free conditions produced substituted 1,4-dihydroquinoline hydroquinones in which the tert-butoxy residue of the BOC group was displaced by a phenolic residue, generating an oxazolone ring that functioned to protect both rings of the dihydroquinoline hydroquinone from untimely oxidation. Oxidative aromatization with concomitant loss of the oxazolone ring was achieved using 2 equiv of o-chloranil in acetic acid and provided substituted quinoline quinones in good yields. By use of this strategy, a concise synthesis of the pyridoacridine ring system was achieved.
