104971-91-7 Usage
Uses
Used in Pharmaceutical Industry:
(E)-1-(2-Hydroxy-5-methyl-phenyl)-3-(5-nitro-furan-2-yl)-propenone is used as a key intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structural features allow it to serve as a building block for the development of new drugs targeting specific diseases or conditions.
Used in Chemical Research:
In the field of chemical research, (E)-1-(2-Hydroxy-5-methyl-phenyl)-3-(5-nitro-furan-2-yl)-propenone is used as a model compound for studying [application reason]. Its structural complexity and functional groups make it an interesting subject for exploring reaction mechanisms, synthetic pathways, and potential transformations.
Used in Material Science:
(E)-1-(2-Hydroxy-5-methyl-phenyl)-3-(5-nitro-furan-2-yl)-propenone is also utilized in material science as a component in the development of novel materials with [application reason]. Its incorporation into polymers or other materials may lead to enhanced properties such as improved stability, reactivity, or specific interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 104971-91-7 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 104971-91:
(8*1)+(7*0)+(6*4)+(5*9)+(4*7)+(3*1)+(2*9)+(1*1)=127
127 % 10 = 7
So 104971-91-7 is a valid CAS Registry Number.
104971-91-7Relevant 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.
