2977-53-9 Usage
Description
Ethanone, 1-(2,3-dichloro-4-hydroxyphenyl)-, also known as 2,3-dichloro-4-hydroxyacetophenone, is a chemical compound that features a unique structure with a ketone group (ethanone) attached to a phenol ring. This structure includes two chlorine atoms at the 2nd and 3rd positions and a hydroxyl group at the 4th position on the phenol ring. Its distinctive molecular composition endows it with potential applications in various fields, including pharmaceuticals and organic synthesis, due to its possible antioxidant, anti-inflammatory, and cytotoxic properties.
Uses
Used in Pharmaceutical Synthesis:
Ethanone, 1-(2,3-dichloro-4-hydroxyphenyl)is utilized as an intermediate in the synthesis of pharmaceuticals for its unique structural properties. The presence of chlorine atoms and a hydroxyl group on the phenol ring allows for versatile chemical reactions, making it a valuable component in the creation of new drug molecules.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, this compound serves as a key building block for the synthesis of various organic compounds. Its reactive sites, including the ketone and hydroxyl groups, facilitate multiple types of chemical reactions, contributing to the development of new organic molecules with potential applications in different industries.
Used in Antioxidant and Anti-Inflammatory Applications:
Due to the presence of the hydroxyl group, Ethanone, 1-(2,3-dichloro-4-hydroxyphenyl)may exhibit antioxidant properties, which could be beneficial in protecting cells from oxidative damage. Additionally, its structure may contribute to anti-inflammatory effects, making it a potential candidate for use in treatments targeting inflammation-related conditions.
Used in Cytotoxic Studies:
The chlorine atoms in the compound may impart cytotoxic effects, which could be harnessed in the development of treatments for cancer or other conditions where the targeted destruction of cells is necessary. Further research is required to explore the full potential of this compound in cytotoxic applications.
Note: The specific applications and industries where Ethanone, 1-(2,3-dichloro-4-hydroxyphenyl)is used are not explicitly mentioned in the provided materials. The uses listed above are inferred based on the compound's properties and potential. Further research and development are needed to confirm these applications and explore additional uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2977-53-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2977-53:
(6*2)+(5*9)+(4*7)+(3*7)+(2*5)+(1*3)=119
119 % 10 = 9
So 2977-53-9 is a valid CAS Registry Number.
2977-53-9Relevant articles and documents
A two-aromatic substituted propylene ketone compound and its preparation method and application (by machine translation)
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, (2019/05/28)
The present invention discloses a two-aromatic substituted propylene ketone compound and its preparation method and application, its structural formula such as formula (I) as shown: Wherein A is B is hydrogen, methyl or ethyl; C is a substituted benzene ring, pyridine and furan heterocyclic, 2 - pyridyl, 3 - pyridyl, 4 - pyridyl, 5 - 1 H - indolyl, 4 - (N, N - dimethylamino) phenyl, 4 - (N - pyrrolyl) phenyl, 4 - [1 - (N - methyl piperazinyl)] phenyl or 4 - (1 - morpholinyl) phenyl. The compounds of the invention has a novel structure, to inhibit the cells MCL active effect, high safety, the preparation cost is low and the like, can be used as a MCL very promising drug. (by machine translation)
(Vinylaryloxy)acetic acids. A new class of diuretic agents. 4. Various [(2 substituted and 2,2 disubstituted vinyl)aryloxy]acetic acids
Woltersdorf Jr.,Robb,Bicking,Watson,Cragoe Jr.
, p. 972 - 975 (2007/10/11)
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