7627-10-3 Usage
Chemical Class
Oxadiazole derivatives
Explanation
1,2,4-Oxadiazol-5(2H)-one, 3-phenyl-, hydrazone belongs to a class of chemical compounds known as oxadiazoles, which are characterized by a five-membered ring containing two nitrogen atoms and one oxygen atom.
Explanation
The compound has potential applications in the pharmaceutical industry due to its antiviral and antibacterial properties, making it a candidate for the development of new drugs to combat infections.
Explanation
Research has shown that 1,2,4-Oxadiazol-5(2H)-one, 3-phenyl-, hydrazone may have therapeutic potential in the treatment of various diseases, including cancer, diabetes, and neurodegenerative disorders, due to its unique chemical structure and biological activity.
Explanation
The unique structure and biological activity of 1,2,4-Oxadiazol-5(2H)-one, 3-phenyl-, hydrazone make it a valuable target for drug development, as it can be further modified and optimized to enhance its therapeutic potential.
Explanation
The compound's structure and potential applications in various disease treatments make it a promising candidate for further research and development in the field of medicinal chemistry, with the aim of creating new and more effective drugs.
Pharmaceutical Applications
Antiviral and Antibacterial Agent
Treatment of Diseases
Cancer, Diabetes, and Neurodegenerative Disorders
Hydrazone Functional Group
Crucial for Biological Activity
Drug Development Target
Valuable for Medicinal Chemistry
Research and Development
Promising Candidate in Medicinal Chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 7627-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7627-10:
(6*7)+(5*6)+(4*2)+(3*7)+(2*1)+(1*0)=103
103 % 10 = 3
So 7627-10-3 is a valid CAS Registry Number.
7627-10-3Relevant articles and documents
Thermal Behaviour of 3-Phenyl-1,2,4-oxadiazol-5-ylhydrazines
Adembri, Giorgio,Camparini, Alfredo,Ponticelli, Fabio,Tedeschi, Piero
, p. 1703 - 1706 (2007/10/02)
Depending on the substitution on the hydrazine moiety, thermolysis of 3-phenyl-1,2,4-oxadiazol-5-ylhydrazines (1)-(5) gives variable amounts of 1-amino-Δ2-1,2,4-triazolin-5-ones (13) or (17), Δ2- or Δ3-1,2,4-triazolin-5-ones (12), (18), or (19), and the s-triazine (20).A possible mechanism accounting for the products and the effects is discussed.A diradical intermediate and a hydrogen transfer from the reaction medium are suggested on the basis of the effect of benzoyl peroxide on the reaction and on the behaviour of the hydrazines (1)-(4) towards catalytic hydrogenation.
