5415-56-5 Usage
Description
(4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one is a complex organic compound characterized by its molecular structure that includes a benzylidene group and an oxazolone ring. (4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one is recognized for its potential biological and pharmacological activities, making it a significant molecule in the realms of medicinal chemistry and drug discovery.
Uses
Used in Pharmaceutical Synthesis:
(4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one is used as a building block for the synthesis of various organic compounds and pharmaceuticals. Its unique structure and functional groups contribute to the development of new drugs with diverse therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one is utilized as a key component in the design and synthesis of novel molecules with potential therapeutic properties. Its derivatives have been investigated for their anti-inflammatory, antitumor, and antimicrobial activities, showcasing its versatility in drug discovery.
Used in Drug Discovery:
(4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one plays a crucial role in drug discovery, as its derivatives exhibit promising biological activities. (4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one's potential applications in treating various diseases, including inflammation, cancer, and infections, make it a valuable asset in the search for new therapeutic agents.
Used in Anticancer Applications:
While not explicitly mentioned in the provided materials, given the compound's potential pharmacological activities and its use in medicinal chemistry, it can be inferred that (4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one may also be used as an anticancer agent. Its derivatives could be employed for their antitumor properties, contributing to the development of novel cancer treatments.
Used in Antimicrobial Applications:
Similarly, the compound's potential antimicrobial properties suggest that (4Z)-4-(3,4-dimethoxybenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one could be used in the development of new antibiotics or antifungal agents, addressing the growing need for novel treatments against drug-resistant infections.
Check Digit Verification of cas no
The CAS Registry Mumber 5415-56-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5415-56:
(6*5)+(5*4)+(4*1)+(3*5)+(2*5)+(1*6)=85
85 % 10 = 5
So 5415-56-5 is a valid CAS Registry Number.
5415-56-5Relevant articles and documents
Design, Synthesis, and Antimicrobial Activity of Novel Fluorine-Containing Imidazolones
Desai,Wadekar,Mehta,Pandit
, p. 976 - 985 (2021/08/09)
Abstract: A simple synthetic protocol have been developed for the preparation of novelN-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydro-1H-imidazol-1-yl)-N′-phenylthiourea derivatives by the reaction of4-benzylidene-2-phenyl-4,5-dihydro-1,3-oxazol-5-ones with N
Novel diamide-based benzenesulfonamides as selective carbonic anhydrase ix inhibitors endowed with antitumor activity: Synthesis, biological evaluation and in silico insights
Abdelrahman, Mohamed A.,Eldehna, Wagdy M.,Nocentini, Alessio,Bua, Silvia,Al-Rashood, Sara T.,Hassan, Ghada S.,Bonardi, Alessandro,Almehizia, Abdulrahman A.,Alkahtani, Hamad M.,Alharbi, Amal,Gratteri, Paola,Supuran, Claudiu T.
, (2019/07/02)
In this work, we present the synthesis and biological evaluation of novel series of diamide-based benzenesulfonamides 5a-h as inhibitors of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1) isoforms hCA I, II, IX and XII. The target tumor-associated i
Microwave-assisted efficient synthesis of azlactones using zeolite NaY as a reusable heterogeneous catalyst
Bodaghifard, Mohammad Ali,Moghanian, Hassan,Mobinikhaledi, Akbar,Esmaeilzadeh, Fatemeh
, p. 845 - 849 (2017/08/10)
The efficient preparation of azlactones in the presence of zeolite NaY has been reported. This heterogeneous catalyst was used for efficient synthesis of azlactone derivatives with Ac2O as a condensing agent under microwave irradiation and solvent-free co
