104971-93-9 Usage
Uses
Used in Organic Synthesis:
(E)-1-(2-Hydroxy-3-methyl-phenyl)-3-(5-nitro-furan-2-yl)-propenone is utilized as an intermediate in organic synthesis for the creation of various complex molecules. Its unique structure, which includes a nitro group and a phenyl group, allows for a range of chemical reactions that can be harnessed to produce desired products.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (E)-1-(2-Hydroxy-3-methyl-phenyl)-3-(5-nitro-furan-2-yl)-propenone is used as a starting material for the development of new pharmaceutical compounds. Its structural features make it a promising candidate for the synthesis of molecules with potential biological and pharmacological activities.
Used in the Development of Novel Drug Delivery Systems:
(E)-1-(2-Hydroxy-3-methyl-phenyl)-3-(5-nitro-furan-2-yl)-propenone may also be employed in the design and development of innovative drug delivery systems. Its chemical properties could be leveraged to improve the bioavailability, targeting, and overall efficacy of therapeutic agents.
Used in Pharmaceutical Industry:
Within the pharmaceutical industry, (E)-1-(2-Hydroxy-3-methyl-phenyl)-3-(5-nitro-furan-2-yl)-propenone is used as a key component in the synthesis of drugs with potential therapeutic applications. Its unique structural elements can be manipulated to create molecules that interact with biological targets, potentially leading to the development of new treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 104971-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,7 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104971-93:
(8*1)+(7*0)+(6*4)+(5*9)+(4*7)+(3*1)+(2*9)+(1*3)=129
129 % 10 = 9
So 104971-93-9 is a valid CAS Registry Number.
104971-93-9Relevant academic research and scientific papers
2'-Hydroxychalcone Analogs of 5-Nitrofurfural and Their Antibacterial Activity
Rao, Chebrolu Papa,Sundaramurthy, V.
, p. 447 - 448 (2007/10/02)
2-Hydroxyacetophenones (I) react with 5-nitrofurfurals (II;X=O) under acid-catalysed conditions to give 2'-hydroxychalcone analogs (III).None of these compounds (III) is found to exhibit significant antibacterial and antifungal activities except 1-(2-hydroxyphenyl)-3-(5-nitro-2-furyl)2-propen-1-one (IIIa) which shows 100percent inhibition against A. niger at 10 ppm concentration.
