575-08-6 Usage
Uses
Used in Pharmaceutical Industry:
6-Fluoronaphthalene-1-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to enhance the properties of drug molecules, such as increasing lipophilicity and metabolic stability, which can improve drug efficacy and bioavailability.
Used in Agrochemical Industry:
In the agrochemical sector, 6-Fluoronaphthalene-1-carboxylic acid is utilized as a precursor in the development of novel agrochemicals, contributing to the creation of more effective and targeted pesticides and herbicides.
Used in Specialty Chemicals:
6-Fluoronaphthalene-1-carboxylic acid is employed as a building block in the synthesis of specialty chemicals, where its unique structure and functional groups can be leveraged to create compounds with specific applications in various industries, such as materials science and fragrances.
Used in Medicinal Chemistry Research:
6-Fluoronaphthalene-1-carboxylic acid is used as a research tool in medicinal chemistry to explore its potential as a scaffold for new drug candidates, particularly in the development of compounds with improved binding affinity and selectivity for biological targets.
Used in Drug Discovery:
As a compound with potential biological activities, 6-Fluoronaphthalene-1-carboxylic acid is utilized in drug discovery processes to identify and optimize lead compounds that can be further developed into effective therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 575-08-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 575-08:
(5*5)+(4*7)+(3*5)+(2*0)+(1*8)=76
76 % 10 = 6
So 575-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H7FO2/c12-8-4-5-9-7(6-8)2-1-3-10(9)11(13)14/h1-6H,(H,13,14)
575-08-6Relevant academic research and scientific papers
A simple route to 6- and 7-fluoro-substituted naphthalene-1-carboxylic acids
Krülle, Thomas M.,Barba, Oscar,Davis, Susan H.,Dawson, Graham,Procter, Martin J.,Staroske, Thomas,Thomas, Gerard H.
, p. 1537 - 1540 (2008/02/02)
A simple one-pot method for the synthesis of 6-fluoro- and 6,7-difluoro-1-naphthoic acid is described. 6-Fluoro-1-naphthoic acid can be converted into 7-fluoro-1-naphthoic acid in three straightforward steps.
DIHYDROIMIDAZOTHIAZOLE DERIVATIVES
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Page/Page column 64, (2008/06/13)
Compounds of formula (I): or pharmaceutically acceptable salts thereof, exhibit 5-HT1A agonism in addition to noradrenaline reuptake inhibition and optionally also 5-HT reuptake inhibition are useful for the treatment of obesity.
Arylpiperazinyl-alkylene-phenyl-heterocyclic compounds
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, (2008/06/13)
Arylpiperazinyl-alkylenephenyl-p-heterocyclic compounds, and the pharmaceutically acceptable acid addition salts thereof are neuroleptic agents. They are useful in the treatment of psychotic disorders.
Arylpiperazinyl-alkylene-phenyl-heterocyclic compounds
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, (2008/06/13)
An arylpiperazinyl-alkylenephenyl-p-heterocyclic compound, useful in the treatment of psychotic disorders, of the formula- or a pharmaceutically-acceptable acid-addition salt thereof,wherein:-, Ar is phenyl, 3-trifluoromethylphenyl, 3-cyanopyridyl, naphth
