63010-70-8 Usage
Uses
Used in Organic Synthesis:
8-Fluoro-4-Hydroxyquinoline-3-Carboxylic Acid is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups enable it to participate in a range of chemical reactions, facilitating the synthesis of novel compounds with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 8-Fluoro-4-Hydroxyquinoline-3-Carboxylic Acid is used as a potential pharmaceutical candidate. Its structural features and chemical properties make it a promising molecule for the development of new drugs, particularly in areas such as antimicrobial, antiviral, and anticancer therapies.
Used in Analytical Chemistry:
8-Fluoro-4-Hydroxyquinoline-3-Carboxylic Acid is used as a fluorescent probe in analytical chemistry. Its property of emitting fluorescence under UV light allows for the detection and quantification of specific analytes in complex samples, making it a valuable tool in areas such as environmental monitoring, forensic science, and biomedical research.
Used in Biochemistry:
8-Fluoro-4-Hydroxyquinoline-3-Carboxylic Acid is used as a functional group in biochemistry. Its carboxylic acid group can be utilized to form esters, amides, and other derivatives, which can then be incorporated into biomolecules or used as intermediates in the synthesis of bioactive compounds.
Used in Fluorescent Labeling:
In the field of molecular biology, 8-Fluoro-4-Hydroxyquinoline-3-Carboxylic Acid is used for fluorescent labeling of biomolecules such as proteins, nucleic acids, and lipids. Its fluorescence property enables the tracking and visualization of these biomolecules within cells or tissues, providing valuable insights into their function and interactions.
Used in Material Science:
8-Fluoro-4-Hydroxyquinoline-3-Carboxylic Acid can be used in the development of advanced materials with specific optical, electronic, or sensing properties. Its incorporation into polymers, nanoparticles, or other materials can result in novel materials with applications in areas such as optoelectronics, sensors, and imaging technologies.
Used in Environmental Science:
In environmental science, 8-Fluoro-4-Hydroxyquinoline-3-Carboxylic Acid can be employed for the detection and monitoring of pollutants or contaminants in water, soil, or air samples. Its fluorescence property allows for the sensitive and selective detection of target analytes, contributing to environmental protection and remediation efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 63010-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,1 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63010-70:
(7*6)+(6*3)+(5*0)+(4*1)+(3*0)+(2*7)+(1*0)=78
78 % 10 = 8
So 63010-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H6FNO3/c11-7-3-1-2-5-8(7)12-4-6(9(5)13)10(14)15/h1-4H,(H,12,13)(H,14,15)
63010-70-8Relevant academic research and scientific papers
4-HYDROXYQUINOLINE-3-CARBOXAMIDES AND HYDRAZIDES AS ANTIVIRAL AGENTS
-
Page/Page column 52, (2010/02/13)
The present invention provides 4-hydroxyquinoline-3-carboxamide and hydrazide compounds of formula I These compounds are useful to treat or prevent the herpesviral infections, particularly, human cytomegaloviral infection.
4-hydroxyquinoline-3-carboxamides and hydrazides as antiviral agents
-
, (2008/06/13)
The present invention provides 4-hydroxyquinoline-3-carboxamide and hydrazide compounds of formula I These compounds are useful to treat or prevent the herpesviral infections, particularly, human cytomegaloviral infection.
Synthesis of fluoro-4-hydroxyquinoline-3-carboxylic acids by the Gould-Jacobs reaction
Leyva, Elisa,Monreal, Elena,Hernandez, Alma
, p. 7 - 10 (2007/10/03)
The synthesis of several fluoro-4-hydroxyquinoline-3-carboxylic acids by the Gould-Jacobs reaction is presented. These quinolines are important intermediates for the preparation of antibacterial fluoroquinolones.
