5449-84-3 Usage
Uses
Used in Organic Synthesis:
[4-[1-(4-acetyloxyphenyl)-3-oxo-isobenzofuran-1-yl]phenyl] acetate is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for specific reactions and transformations that can lead to the development of new compounds with tailored properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [4-[1-(4-acetyloxyphenyl)-3-oxo-isobenzofuran-1-yl]phenyl] acetate is used as a potential active pharmaceutical ingredient (API). Its complex molecular structure may offer novel therapeutic effects, and further research could reveal its potential in treating specific diseases or conditions.
Used in Materials Science:
[4-[1-(4-acetyloxyphenyl)-3-oxo-isobenzofuran-1-yl]phenyl] acetate is utilized in materials science for the development of new materials with unique properties. Its incorporation into polymers or other materials could lead to advancements in areas such as electronics, coatings, or specialty chemicals, where its specific characteristics may provide enhanced performance or new functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 5449-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5449-84:
(6*5)+(5*4)+(4*4)+(3*9)+(2*8)+(1*4)=113
113 % 10 = 3
So 5449-84-3 is a valid CAS Registry Number.
5449-84-3Relevant academic research and scientific papers
Visible Light-Promoted Magnesium, Iron, and Nickel Catalysis Enabling C(sp3)-H Lactonization of 2-Alkylbenzoic Acids
Li, Sasa,Su, Mincong,Sun, Jie,Hu, Kunjun,Jin, Jian
supporting information, p. 5842 - 5847 (2021/07/31)
A mild and practical C(sp3)-H lactonization protocol has been achieved by merging photocatalysis and magnesium (iron, nickel) catalysis. A diverse range of 2-alkylbenzoic acids with a variety of substitution patterns could be transformed into the corresponding phthalide products. Based on the mechanistic experimentation and reported prior studies, a possible mechanism for the benzylic oxidative lactonization reaction was proposed with the hypothetic photoactive ternary complex formed between the 2-alkylbenzoic acid substrate, magnesium ion, and bromate anion.
A rapid and efficient method for acetylation of phenols with acetic anhydride catalysed by TiO2/SO42- solid superacid
Ma, Yan-Ran,Jin, Tong-Shou,Wang, Zhen-Hua,Li, Tong-Shuang
, p. 1777 - 1778 (2007/10/03)
A rapid and efficient method for acetylation of phenols with acetic anhydride in the presence of TiO2/SO42- solid superacid at room or at reflux temperature in excellent yield is described.
