14192-12-2 Usage
Uses
Used in Analytical Chemistry:
2,5-Diiodobenzoic Acid is used as a reagent for the detection and response of divergent compounds that are strong electron absorbers. This application is particularly relevant in gas chromatography with electron capture detection, where its electron-absorbing properties enhance the sensitivity and accuracy of the analysis.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-Diiodobenzoic Acid may be utilized as an intermediate in the synthesis of various drugs, taking advantage of its unique chemical properties to create novel therapeutic agents.
Used in Environmental Monitoring:
2,5-Diiodobenzoic Acid can be employed in environmental monitoring applications, where its ability to detect electron-absorbing compounds can be used to identify and quantify pollutants or contaminants in air, water, or soil samples.
Used in Material Science:
In material science, 2,5-Diiodobenzoic Acid may be used in the development of new materials with specific electronic properties, such as semiconductors or sensors, by incorporating its strong electron-absorbing characteristics into the material's structure.
Biochem/physiol Actions
2,5-Diiodobenzoic acid forms 1:1 complex with cycloheptaamylose. It undergoes palladium-catalyzed coupling reaction with terminal alkynes.
Check Digit Verification of cas no
The CAS Registry Mumber 14192-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,9 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14192-12:
(7*1)+(6*4)+(5*1)+(4*9)+(3*2)+(2*1)+(1*2)=82
82 % 10 = 2
So 14192-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H4I2O2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,(H,10,11)
14192-12-2Relevant articles and documents
Synthesis method of 2-halogen-5-iodobenzoic acid
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Paragraph 0043-0047; 0051; 0052, (2019/09/17)
The invention discloses a synthesis method of 2-halogen-5-iodobenzoic acid. The synthesis method comprises steps as follows: o-halogen benzoic acids are subjected to one-step iodo treatment in an iodio reagent, and 2-halogen-5-iodobenzoic acid is obtained. Aftertreatment comprises steps as follows: a reaction liquid is poured into a cold reductive water solution and quenched, a solvent is evaporated to dryness, recrystallization and filtration are performed, and a product can be obtained. The method is short in reaction route, simple to operate, environmentally friendly, safer and more economical and has broad application prospects.
Tetraalkylammonium dichloroiodates as iodinating agents: Absence of activity in solid phases and superelectrophilic activity in sulfuric acid
Filimonov, Victor D.,Semenischeva, Nadya I.,Krasnokutskaya, Elena A.,Ho, Yun Hwang,Chi, Ki-Whan
, p. 401 - 404 (2008/09/20)
In contrast to published results, tetraalkylammonium dichloroiodates (Alk4N+ICl2-) cannot be iodinating reagents for arenes in solvent-free conditions. Nevertheless, tetraalkylammonium dichloroiodates in sulfuric acid solutions or in the presence of Ag 2SO4 in H2SO4 possess superelectrophilic properties and act as very convenient and efficient iodinating agents for deactivated arenes. Georg Thieme Verlag Stuttgart.
