24962-84-3 Usage
Uses
Used in Fragrance and Flavoring Industry:
(5E)-5-(4-methoxybenzylidene)furan-2(5H)-one is used as a fragrance and flavoring agent due to its pleasant aroma, adding value to various products in this industry by enhancing their sensory appeal.
Used in Pharmaceutical Applications:
(5E)-5-(4-methoxybenzylidene)furan-2(5H)-one is used as a potential active pharmaceutical ingredient for its demonstrated antifungal and antibacterial properties, contributing to the development of new treatments for various infections and diseases.
Used in Chemical Research:
(5E)-5-(4-methoxybenzylidene)furan-2(5H)-one is also utilized as a subject of study in chemical research, where it can provide insights into the properties and behaviors of furan derivatives, potentially leading to the discovery of new compounds with specialized applications.
Check Digit Verification of cas no
The CAS Registry Mumber 24962-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24962-84:
(7*2)+(6*4)+(5*9)+(4*6)+(3*2)+(2*8)+(1*4)=133
133 % 10 = 3
So 24962-84-3 is a valid CAS Registry Number.
24962-84-3Relevant academic research and scientific papers
Synthesis of new aryl substituted furan-2(5H)-ones using the Suzuki-Miyaura reaction
Zhang, Ruonan,Iskander, George,Da Silva, Paulo,Chan, Daniel,Vignevich, Valentina,Nguyen, Vi,Bhadbhade, Mohan M.,Black, David Stc,Kumar, Naresh
experimental part, p. 3010 - 3016 (2011/05/02)
A series of novel 5-arylidenefuran-2(5H)-ones and 5-arylidene-4-arylfuran- 2(5H)-ones were synthesized via the Suzuki-Miyaura reactions of fimbrolide derivatives 5-(bromomethylene)furan-2(5H)-one and 4-bromo-5-(bromomethylene) furan-2(5H)-one, respectivel
A new, highly stereoselective synthesis of β-unsubstituted (Z)-γ-alkylidene-butenolides using bromine as a removable stereocontrol element
Boukouvalas, John,Beltrán, Paola P.,Lachance, Nicolas,C?té, Sébastien,Maltais, Fran?ois,Pouliot, Martin
, p. 219 - 222 (2007/10/03)
Several β-unsubstituted (Z)-γ-alkylidenebutenolides have been prepared in highly stereocontrolled fashion by implementing a steric directing group stratagem in the vinylogous aldol condensation of butenolides with aldehydes. Applications to the synthesis of the antitumor heptene (S)-melodorinol and a thiophenelactone from Chamaemelum nobile L. are described. Georg Thieme Verlag Stuttgart.
