4707-24-8 Usage
Uses
Used in Pharmaceutical Industry:
4-BROMO-2,3,5,6-TETRAFLUOROBENZOIC ACID is used as a pharmaceutical intermediate for the synthesis of various drugs. Its chemical properties allow it to be a key component in the development of new medications, contributing to the advancement of pharmaceutical research and drug discovery.
As a Building Block for Drug Synthesis:
4-BROMO-2,3,5,6-TETRAFLUOROBENZOIC ACID is used as a building block in the creation of complex pharmaceutical compounds. Its bromine and fluorine atoms can be further functionalized or modified to produce a wide range of drug candidates with potential therapeutic applications.
In Medicinal Chemistry Research:
4-BROMO-2,3,5,6-TETRAFLUOROBENZOIC ACID is utilized in medicinal chemistry research to explore its potential as a precursor to novel drug molecules. Its unique structure offers opportunities for the development of new therapeutic agents, particularly in the areas of anti-inflammatory, analgesic, and anti-cancer drugs.
In Drug Design and Optimization:
4-BROMO-2,3,5,6-TETRAFLUOROBENZOIC ACID is employed in drug design and optimization processes to improve the efficacy, safety, and pharmacokinetic properties of drug candidates. Its versatile chemical structure allows for the fine-tuning of drug molecules to achieve better therapeutic outcomes.
In Drug Synthesis Method Development:
4-BROMO-2,3,5,6-TETRAFLUOROBENZOIC ACID is used in the development of new synthetic methods and techniques for the production of pharmaceutical compounds. Its unique properties can be leveraged to streamline the synthesis process, reduce costs, and improve the overall efficiency of drug manufacturing.
In Quality Control and Analysis:
4-BROMO-2,3,5,6-TETRAFLUOROBENZOIC ACID is also used in the quality control and analysis of pharmaceutical products. Its distinct chemical properties make it a valuable reference compound for the assessment of purity, stability, and other critical quality attributes of drug substances and formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 4707-24-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4707-24:
(6*4)+(5*7)+(4*0)+(3*7)+(2*2)+(1*4)=88
88 % 10 = 8
So 4707-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H2BrF4NO/c8-2-5(11)3(9)1(7(13)14)4(10)6(2)12/h(H2,13,14)
4707-24-8Relevant academic research and scientific papers
Facile synthesis and supramolecular chemistry of hydrogen bond/halogen bond-driven multi-tasking tectons
Aakeroey, Christer B.,Chopade, Prashant D.,Ganser, Claudia,Desper, John
experimental part, p. 4688 - 4690 (2011/06/20)
Hydrogen bonds and halogen bonds can be used as synthetic vectors without structural interference as long as the primary molecular recognition events are designed around a careful combination of geometric and electrostatic complementarity. In addition, a one-step procedure for the synthesis of tectons equipped with powerful hydrogen- and halogen-bond donors is presented. The Royal Society of Chemistry 2011.
INHIBITORS OF STEAROYL-COA DESATURASE
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, (2009/06/27)
Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity.
Pyridinyl-quinolone compounds, their preparation and use
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, (2008/06/13)
Fluorinated 1-cyclopropyl-7-(substituted-pyridinyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids of the formula STR1 wherein R is hydrogen, R' and R" are hydrogen or fluoro, or other groups and Z is 3- or 4-pyridinyl substituted by alkyl groups or substituted alkyl groups, are superior antibacterial agents. They are prepared via a coupling reaction between the corresponding esters (R=alkyl) having a halo group in the 7-position and a substituted (trialkylstannyl)pyridine.
Pesticidal compounds
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, (2008/06/13)
Bicyclooctane pesticides of the formula are prepared by cyclisation of In these formulae R may be various organic groups and is preferably n-butyl or n-propyl while R2 is a polysubstituted phenyl group.
