923722-86-5 Usage
Uses
Used in Organic Synthesis:
2-Bromo-5-fluoro-N-(fur-2-ylmethyl)Benzamide is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structural features allow for the formation of new molecules with potential applications in different fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Bromo-5-fluoro-N-(fur-2-ylmethyl)Benzamide is used as a starting material for the development of potential pharmaceuticals. Its diverse biological activities, including antimicrobial and antifungal properties, make it a valuable compound for designing new drugs.
Used in Antimicrobial Applications:
2-Bromo-5-fluoro-N-(fur-2-ylmethyl)Benzamide is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms. Its unique chemical structure contributes to its effectiveness in combating bacterial and fungal infections.
Used in Antifungal Applications:
In antifungal applications, 2-Bromo-5-fluoro-N-(fur-2-ylmethyl)Benzamide is used to treat fungal infections by inhibiting the growth and proliferation of fungi. Its chemical properties make it a potent antifungal agent.
Used in Anticancer Research:
2-Bromo-5-fluoro-N-(fur-2-ylmethyl)Benzamide is used as a potential anticancer agent in research settings. Its ability to target and inhibit the growth of cancer cells makes it a promising candidate for the development of new cancer therapies.
Used in Drug Design:
2-Bromo-5-fluoro-N-(fur-2-ylmethyl)Benzamide is used as a valuable tool in drug design for the study of structure-activity relationships. Its unique structural features provide insights into the design of more effective and targeted pharmaceuticals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Bromo-5-fluoro-N-(fur-2-ylmethyl)Benzamide is used as a key intermediate in the synthesis of various drugs. Its diverse biological activities and potential applications in antimicrobial, antifungal, and anticancer therapies make it an essential compound in the development of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 923722-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,7,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 923722-86:
(8*9)+(7*2)+(6*3)+(5*7)+(4*2)+(3*2)+(2*8)+(1*6)=175
175 % 10 = 5
So 923722-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H9BrFNO2/c13-11-4-3-8(14)6-10(11)12(16)15-7-9-2-1-5-17-9/h1-6H,7H2,(H,15,16)
923722-86-5Relevant academic research and scientific papers
Liu, Hailong,Han, Weibiao,Li, Chun,Ma, Zhiyong,Li, Ruixiang,Zheng, Xueli,Fu, Haiyan,Chen, Hua
, p. 389 - 393 (2016)
A highly efficient construction of phenanthridinone derivatives from o-halobenzamides was developed by using a phosphine-free palladium catalyst in N,N-dimethylacetamide. The domino reaction proceeds through a sequential C-C and C-N bond-formation process in one pot. This protocol exhibits broad substrate scope and affords a series of phenanthridinones in up to 93 % yield. Importantly, the protocol could also be applied for the less reactive o-chlorobenzamides. The approach constitutes the first example of the synthesis of phenanthridinones from this kind of substrate. Moreover, the success of a gram-scale reaction demonstrated that this operationally simple process is scalable.
