38899-20-6 Usage
Uses
Used in Pharmaceutical Research:
(E)-3-[5-(4-bromophenyl)furan-2-yl]-1-phenylprop-2-en-1-one is used as a key compound in pharmaceutical research for its potential to exhibit a range of pharmacological properties. These include anti-inflammatory, antimicrobial, antioxidant, and anticancer activities, which make it a promising candidate for the development of new drugs and treatments.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-3-[5-(4-bromophenyl)furan-2-yl]-1-phenylprop-2-en-1-one serves as an important intermediate or building block for the creation of more complex molecules with specific biological functions. Its unique structure allows for further modification and functionalization, contributing to the advancement of chemical libraries and the discovery of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 38899-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,9 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38899-20:
(7*3)+(6*8)+(5*8)+(4*9)+(3*9)+(2*2)+(1*0)=176
176 % 10 = 6
So 38899-20-6 is a valid CAS Registry Number.
38899-20-6Relevant academic research and scientific papers
Synthesis of novel arylfurfurylchalcones
Aslam, Samina,Asif, Nadia,Khan, Muhammad Naeem,Khan, Misbahul Ain,Munawar, Munawar Ali,Nasrullah, Muhammad
, p. 7738 - 7742 (2013/09/23)
Various aryl furans-2-carbaldehyde chalcones with different acetophenones were prepared and characterized through their elemental analyses and spectroscopic techniques (FTIR, 1H NMR, 13C NMR and mass spectra).
Studies on arylfuran derivatives Part X. Synthesis and antibacterial properties of arylfuryl-Δ2-pyrazolines
Shivarama Holla,Akberali,Shivananda
, p. 256 - 263 (2007/10/03)
Arylfurylpropenones 3 were synthesized by Claisen-Schmidt condensation of arylfurfurals 1 with various substituted acetophenones 2. Cyclocondensation of these arylfurylpropenones 3 with hydrazine hydrate and phenylhydrazine furnished 1H-pyrazolines 4 and N-phenylpyrazolines 6, respectively. In order to study the structure-activity relationships, pyrazolines 4 were converted into their N-acetyl derivatives 5. The antibacterial properties of the new pyrazoline derivatives were studied. (C) 2000 Elsevier Science S.A.
