15482-69-6 Usage
Description
(5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE is a chemical compound characterized by a benzofuran ring system and a ketone functionality attached to a phenyl group. (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE is known for its potential applications in various fields due to the presence of bromine and benzofuran moieties, which can enhance biological activity and interactions with specific biological targets. The phenyl group also allows for further derivatization and modification of the molecule's properties.
Uses
Used in Pharmaceutical Research:
(5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE is used as a key intermediate in the synthesis of new drugs for various therapeutic applications. The presence of the bromine and benzofuran moieties makes it a promising candidate for drug discovery, as they can improve the compound's interaction with specific biological targets.
Used in Agrochemical Development:
In the agrochemical industry, (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE is used as a building block for the development of new agrochemicals. Its unique structure and functional groups can be exploited to create compounds with enhanced biological activity and selectivity, potentially leading to more effective and environmentally friendly products.
Used in Materials Science:
(5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE also has potential applications in materials science, where its unique structure and properties can be utilized to develop new materials with specific characteristics. (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE's versatility in terms of derivatization and modification makes it an attractive candidate for research in this field.
It is important to handle and use (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE with caution, following proper safety protocols and regulations to ensure the safety of researchers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 15482-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,8 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15482-69:
(7*1)+(6*5)+(5*4)+(4*8)+(3*2)+(2*6)+(1*9)=116
116 % 10 = 6
So 15482-69-6 is a valid CAS Registry Number.
15482-69-6Relevant articles and documents
Reaction of chalcones with NBS, a simple one pot synthesis of 2-aroylbenzo[b]furanes
Litkei, Gyoergy,Gulacsi, Katalin,Antus, Sandor,Dinya, Zoltan
, p. 3061 - 3074 (1996)
A simple one pot synthesis of 2-aroylbenzo[b]furanes has been achieved by bromomethoxylation with NBS and subsequent treatment of the appropriately substituted 2-hydroxychalcones with sodium hydroxide.
Copper(I)-Catalyzed Chemoselective Reduction of Benzofuran-2-yl Ketones to Alcohols with B2pin2 via a Domino-Borylation-Protodeboronation Strategy
Xuan, Qingqing,Kong, Weiguang,Song, Qiuling
, p. 7602 - 7607 (2017/07/26)
A novel copper(I)-catalyzed chemoselective reduction of the carbonyls of benzofuran-2-yl ketones over furan rings with B2pin2 has been developed. This reaction proceeded under mild conditions. High valuable secondary alcohol derivatives of benzofurans were obtained in good to excellent yields with a broad substrate scope. The mechanistic studies suggested that a domino-borylation-protodeboronation pathway was involved in this reaction.
Synthesis and antitubercular activity of 4-thiazolidinone derivatives incorporating benzofuran moiety
Basawaraj, Raga,Channamma,Sangmeshwar
, p. 59 - 66 (2019/01/21)
5-Bromo-1-benzofuran-2-yl(substituted phenyl) methanones (2a-e) were prepared by the reaction of 2-bromo-1-(phenyl) ethanones and 5-bromosalicylaldehyde in dimethylformamide in the presence of anhydrous potassium carbonate to maintain basic condition. Con
