58416-46-9 Usage
Uses
Used in Pharmaceutical Industry:
6-Nitroquinolin-5-ol is used as an active pharmaceutical ingredient for its antimicrobial, anti-inflammatory, and antitumor properties, contributing to the development of new drugs that can treat various diseases and conditions.
Used in Agrochemical Industry:
6-Nitroquinolin-5-ol is used as an active ingredient in agrochemicals, leveraging its antimicrobial properties to protect crops from harmful pathogens and enhance agricultural productivity.
Used in Chemical Manufacturing:
6-Nitroquinolin-5-ol is used as an intermediate in the production of dyes, pigments, and other organic compounds, contributing to the development of new and improved products in the chemical industry.
Used in Research and Development:
6-Nitroquinolin-5-ol is used as a research compound in laboratories, where its unique properties are studied and explored for potential applications in various fields, including medicine, agriculture, and chemical manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 58416-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58416-46:
(7*5)+(6*8)+(5*4)+(4*1)+(3*6)+(2*4)+(1*6)=139
139 % 10 = 9
So 58416-46-9 is a valid CAS Registry Number.
58416-46-9Relevant academic research and scientific papers
Hydroxylation of Nitroarenes with Alkyl Hydroperoxide Anions via Vicarious Nucleophilic Substitution of Hydrogen
Makosza, Mieczyslaw,Sienkiewicz, Krzysztof
, p. 4199 - 4208 (2007/10/03)
Rhone-Poulenc Polska Ltd., ul. Grzybowska 80/82, 00-844 Warszawa, Poland Garbo- and heterocyclic nitroarenes react with anions of tert-butyl and cumyl hydroperoxides in the presence of strong bases to form substituted o- and p-nitrophenols. The reaction usually proceeds in high yields and is of practical value as a method of synthesis and manufacturing of nitrophenols. Orientation of the hydroxylation can be controlled to a substantial extent by selection of the proper conditions. Basic mechanistic features of this process were clarified.
Process for the hydroxylation of electrophilic aromatic compounds
-
, (2008/06/13)
The invention relates to a generally applicable process for the hydroxylation of electrophilic aromatic compounds, according to which the electrophilic aromatic compounds are reacted with organic hydroperoxides in the presence of bases.
