89047-45-0 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
2-Quinolinecarboxylic acid hydrochloride is used as a building block for the synthesis of various pharmacological agents. Its role in creating new drugs is significant due to its ability to be incorporated into diverse molecular structures, contributing to the development of novel therapeutics.
Used in Anti-Inflammatory Applications:
2-Quinolinecarboxylic acid hydrochloride is studied for its potential anti-inflammatory properties, making it a candidate for the treatment of conditions characterized by inflammation. Its capacity to modulate inflammatory responses could be beneficial in managing a range of diseases.
Used in Antiviral Applications:
2-Quinolinecarboxylic acid hydrochloride is also being investigated for its potential antiviral properties, which could lead to the development of treatments for viral infections. Its antiviral activity may be leveraged to inhibit the replication or infectivity of certain viruses.
Used in Antitumor Applications:
2-Quinolinecarboxylic acid hydrochloride has been studied for its potential antitumor properties, indicating its possible use in cancer therapy. Its ability to target and affect tumor cells could contribute to the development of new cancer treatments.
Used in the Production of Dyes:
In the dye industry, 2-Quinolinecarboxylic acid hydrochloride is used as a chemical intermediate for the production of various dyes. Its chemical structure allows for the creation of colorants with specific properties.
Used in the Production of Pesticides:
2-Quinolinecarboxylic acid hydrochloride is also utilized in the synthesis of pesticides, where it may contribute to the development of compounds that control, repel, or kill pests.
Used in the Production of Other Organic Chemicals:
Beyond the aforementioned applications, 2-Quinolinecarboxylic acid hydrochloride is a versatile intermediate in the synthesis of a range of other organic chemicals, highlighting its importance in the broader chemical industry.
It is important to handle 2-Quinolinecarboxylic acid hydrochloride with care, as it can be harmful if ingested or inhaled. Proper safety precautions should be followed when working with this chemical to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 89047-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,4 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89047-45:
(7*8)+(6*9)+(5*0)+(4*4)+(3*7)+(2*4)+(1*5)=160
160 % 10 = 0
So 89047-45-0 is a valid CAS Registry Number.
89047-45-0Relevant articles and documents
One-pot friedlnder quinoline synthesis: Scope and limitations
Li, An-Hu,Beard, David J.,Coate, Heather,Honda, Ayako,Kadalbajoo, Mridula,Kleinberg, Andrew,Laufer, Radoslaw,Mulvihill, Kristen M.,Nigro, Anthony,Rastogi, Pawan,Sherman, Dan,Siu, Kam W.,Steinig, Arno G.,Wang, Ti,Werner, Doug,Crew, Andrew P.,Mulvihill, Mark J.
experimental part, p. 1678 - 1686 (2010/06/22)
A highly effective one-pot Friedlnder quinoline synthesis from o-nitroarylcarbaldehydes and ketones or aldehydes was developed and the scope and limitations of the method were examined. The o-nitroarylcarbaldehydes were reduced to o-aminoarylcarbaldehydes with iron in the presence of a catalytic amount of aqueous hydrochloric acid; the amino compounds were then condensed in situ with ketones or aldehydes to form mono- or disubstituted quinolines, respectively, in good-to-excellent yields (58-100%). Georg Thieme Verlag Stuttgart - New York.
