96195-89-0 Usage
Uses
Used in Organic Synthesis:
Diphenyliodonium-2-carboxylate monohydrate is used as a reagent for the synthesis of aryl ketones and carboxylic acids. Its electrophilic iodine character enables efficient and selective transformations in organic chemistry, making it a valuable tool for the preparation of complex organic molecules.
Used in Oxidation Reactions:
As a source of electrophilic iodine, diphenyliodonium-2-carboxylate monohydrate is employed in oxidation reactions, where it can selectively oxidize various organic substrates. This property makes it a useful reagent for the synthesis of functionalized organic compounds and the introduction of oxygen-containing groups.
Used in Functional Group Interconversions:
Diphenyliodonium-2-carboxylate monohydrate is utilized in the interconversion of functional groups, allowing chemists to modify the structure of organic molecules and access a broader range of chemical entities. Its ability to facilitate such transformations contributes to its versatility in organic synthesis.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, diphenyliodonium-2-carboxylate monohydrate is used as a reagent for the synthesis of bioactive compounds and drug candidates. Its ability to participate in various organic transformations enables the development of novel therapeutic agents with improved pharmacological properties.
Used in Material Science:
In material science, diphenyliodonium-2-carboxylate monohydrate is employed in the synthesis of functional materials, such as polymers and organic semiconductors. Its role in organic transformations allows for the creation of materials with tailored properties for specific applications, such as energy storage, sensing, and optoelectronics.
Overall, diphenyliodonium-2-carboxylate monohydrate is a multifaceted chemical reagent with a wide range of applications in various fields, including organic synthesis, pharmaceuticals, and material science. Its unique properties and reactivity make it an indispensable tool for chemists and researchers working in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 96195-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,9 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96195-89:
(7*9)+(6*6)+(5*1)+(4*9)+(3*5)+(2*8)+(1*9)=180
180 % 10 = 0
So 96195-89-0 is a valid CAS Registry Number.
