187679-62-5 Usage
Description
6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline is a chemical compound with the molecular formula C12H13NO2. It is an aromatic organic compound and belongs to the class of quinolone alkaloids. 6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline is synthesized through the methylation and oxidation of 6-methoxy-1-methyl-1,2,3,4-tetrahydroquinoline. It is recognized for its potential pharmacological activities and is often utilized as a building block in organic synthesis, particularly for the production of pharmaceuticals and agrochemicals. Additionally, it has been reported to possess antioxidant and anti-inflammatory properties, which position it as a potential candidate for treating oxidative stress-related conditions.
Uses
Used in Pharmaceutical Industry:
6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs targeting a range of diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline serves as a fundamental building block for the creation of novel agrochemicals. Its incorporation into these products can enhance their effectiveness in agricultural applications.
Used in Antioxidant Applications:
6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline is utilized as an antioxidant, helping to combat oxidative stress and related conditions. Its antioxidant properties make it a promising candidate for the development of treatments aimed at reducing oxidative damage in various diseases.
Used in Anti-Inflammatory Applications:
6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline is also used for its anti-inflammatory properties, which can be beneficial in the management of inflammation-related disorders. Its potential to reduce inflammation makes it a candidate for inclusion in therapeutic agents for such conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 187679-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,6,7 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 187679-62:
(8*1)+(7*8)+(6*7)+(5*6)+(4*7)+(3*9)+(2*6)+(1*2)=205
205 % 10 = 5
So 187679-62-5 is a valid CAS Registry Number.
187679-62-5Relevant articles and documents
Rhodium(III)-catalyzed N-nitroso-directed C-H olefination of arenes. High-yield, versatile coupling under mild conditions
Liu, Baoqing,Fan, Yang,Gao, Yang,Sun, Chao,Xu, Cheng,Zhu, Jin
, p. 468 - 473 (2013/02/23)
N-Nitroso compounds are a versatile class of organic structures that allow expedient access to a diversity of synthetically useful architectures through demonstrated reactivities. We report herein the development of a Rh(III)-catalyzed N-nitroso-directed
Substituted benzolactam compounds as substance P antagonists
-
, (2008/06/13)
Compounds of the formula are effective for the treatment of conditions in mammals which require inhibition of the action of substance P.
