22115-39-5 Usage
Description
1(3H)-Isobenzofuranone, 3-benzoyl-3-hydroxyis a chemical compound with the molecular formula C14H10O3. It is a derivative of isobenzofuranone and features a benzoyl group and a hydroxy group attached to the third carbon atom. 1(3H)-Isobenzofuranone, 3-benzoyl-3-hydroxyis known for its versatile reactivity and functional groups, making it a valuable component in the synthesis of pharmaceuticals and agrochemicals. It also holds potential in the development of new materials and serves as a reagent in organic synthesis. Furthermore, it has been investigated for its biological activities and possible pharmacological properties, highlighting its significance across various industries.
Uses
Used in Pharmaceutical Synthesis:
1(3H)-Isobenzofuranone, 3-benzoyl-3-hydroxyis used as a key intermediate for the synthesis of various pharmaceuticals. Its unique structure and functional groups allow for the creation of a wide range of therapeutic compounds, contributing to the development of new medications.
Used in Agrochemical Production:
In the agrochemical industry, 1(3H)-Isobenzofuranone, 3-benzoyl-3-hydroxyis utilized as a starting material for the production of various agrochemicals. Its reactivity and functional groups enable the synthesis of compounds that can be used in the development of pesticides, herbicides, and other agricultural products.
Used in Material Development:
1(3H)-Isobenzofuranone, 3-benzoyl-3-hydroxyis also used as a building block in the development of new materials. Its structural properties and reactivity make it a promising candidate for creating innovative materials with specific characteristics for various applications.
Used in Organic Synthesis as a Reagent:
1(3H)-Isobenzofuranone, 3-benzoyl-3-hydroxyserves as a valuable reagent in organic synthesis, facilitating various chemical reactions and contributing to the formation of complex organic molecules.
Used in Biological Research and Pharmacology:
Due to its potential biological activities and pharmacological properties, 1(3H)-Isobenzofuranone, 3-benzoyl-3-hydroxyis used in research to explore its effects on biological systems and its possible applications in medicine. This includes studying its interactions with biological targets and evaluating its efficacy in treating specific conditions or diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 22115-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,1 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22115-39:
(7*2)+(6*2)+(5*1)+(4*1)+(3*5)+(2*3)+(1*9)=65
65 % 10 = 5
So 22115-39-5 is a valid CAS Registry Number.
22115-39-5Relevant articles and documents
Ozonolysis of enol ethers. Part 10. Ozonization of enol ethers from 1,2- and 1,3-dicarbonyl compounds: Direct quantitative synthesis of phthalonic acid anhydride
Schank, Kurt,Beck, Horst,Pistorius, Susanne
, p. 2025 - 2049 (2007/10/03)
The results of ozonolyses of enol ethers from 1.2- and 1.3-dicarbonyl compounds presented here strongly indicate that these reactions do not proceed via the established Criegee ozonolysis mechanism for nucleophilic C=C bonds. The quantitative one-step synthesis of phthalonic acid anhydride via ozonolysis of 2-(methoxymethyliden)-1H-inden-1.3(2H)-dione (28a) is described. Furthermore, a revision of the theory of alkene ozonolysis in the presence of tetracyanoethylene (TCNE) is proposed on the basis of a single-electron-transfer (SET) chemistry.
