24523-53-3 Usage
Uses
Used in Pharmaceutical Research:
1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used as a research compound for its potential pharmacological activities. Its unique structure and properties make it a valuable tool in the development of new drugs and therapies.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone serves as a key intermediate or building block for the synthesis of more complex molecules. Its reactivity and versatility contribute to the creation of a wide range of chemical products.
Used in Antimicrobial Applications:
1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used as an antimicrobial agent due to its ability to inhibit the growth of various microorganisms. This property makes it a valuable asset in the development of new antibiotics and antifungal agents.
Used in Antitumor Applications:
In the field of oncology, 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used as an antitumor agent. Its potential to target and inhibit the growth of cancer cells makes it a promising candidate for the development of novel cancer treatments.
Used in Drug Development:
1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone's structure and properties make it a valuable candidate for drug development. Researchers can use 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone as a starting point to design and synthesize new drugs with improved efficacy and selectivity.
Used in Medicinal Chemistry:
In medicinal chemistry, 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used to study the structure-activity relationship of various biologically active molecules. This knowledge can be applied to optimize the design of new drugs with better pharmacokinetic and pharmacodynamic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 24523-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24523-53:
(7*2)+(6*4)+(5*5)+(4*2)+(3*3)+(2*5)+(1*3)=93
93 % 10 = 3
So 24523-53-3 is a valid CAS Registry Number.
24523-53-3Relevant academic research and scientific papers
Rapid and Atom Economic Synthesis of Isoquinolines and Isoquinolinones by C–H/N–N Activation Using a Homogeneous Recyclable Ruthenium Catalyst in PEG Media
Deshmukh, Dewal S.,Gangwar, Neha,Bhanage, Bhalchandra M.
supporting information, p. 2919 - 2927 (2019/05/10)
Herein, we report an atom-efficient, rapid, green, and sustainable approach to synthesize isoquinolines and isoquinolinones using a homogeneous recyclable ruthenium catalyst in PEG Media assisted by microwave energy. Dibenzoylhydrazine was used for C–H/N–N activation reactions for the first time in combination with ketazine as oxidizing directing groups for annulation reactions with internal alkynes. The developed protocol is environmentally benign due to significantly shortened times with an easy extraction method, higher atom economy, external oxidant and silver or antimony salt free conditions, applicability to a gram scale synthesis, use of biodegradable solvent and wide substrate scope with higher product yields. Moreover, it is worth noting that the established methodology allowed reuse of the catalytic system for up to five successive runs with minimal loss in activity.
Reactions of 1,3-dipolar aldazines and ketazines with the dipolarophile dimethyl acetylenedicarboxylate
El-Alali, Abdullah,Al-Kamali, Ahmed S.
, p. 1293 - 1301 (2007/10/03)
The prepared aldazines (aldehyde azines) and ketazines (ketone azines) were allowed to react with 2 mol of the acetylene derivative. The first products formed were pentalene azine derivatives, which in some cases underwent skeletal rearrangment into acycl
