3839-82-5 Usage
Description
1-(3-Phenyl-2-propenylidene)semicarbazide, also known as semicarbazones, is a chemical compound with the molecular formula C10H12N4. It is a derivative of semicarbazide and is characterized by its yellow crystalline solid appearance and a mild odor. 1-(3-Phenyl-2-propenylidene)semicarbazide is soluble in organic solvents such as ethanol and acetone, and it has been the subject of research for its potential biological activities, which include anti-cancer, antimicrobial, and antiviral properties. Furthermore, 1-(3-Phenyl-2-propenylidene)semicarbazide is valued for its use as a reagent in the synthesis of other organic compounds due to its ability to form stable complexes with metal ions.
Uses
Used in Pharmaceutical Research:
1-(3-Phenyl-2-propenylidene)semicarbazide is used as a key compound in pharmaceutical research for its potential anti-cancer properties. It is being studied for its ability to target and inhibit the growth of cancer cells, making it a promising candidate for the development of novel cancer treatments.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(3-Phenyl-2-propenylidene)semicarbazide is utilized as a reagent for the synthesis of other organic compounds. Its capacity to form stable complexes with metal ions makes it a valuable component in the creation of various chemical products.
Used in Antimicrobial Applications:
1-(3-Phenyl-2-propenylidene)semicarbazide is also being explored for its antimicrobial properties, which could lead to its use in the development of new antibiotics or antifungal agents to combat drug-resistant infections.
Used in Antiviral Applications:
Due to its potential antiviral properties, 1-(3-Phenyl-2-propenylidene)semicarbazide may be employed in the development of new antiviral medications, particularly in the context of emerging viral threats and the need for innovative treatment options.
Used in Chemical Reagent Formulation:
As a reagent that can form stable complexes with metal ions, 1-(3-Phenyl-2-propenylidene)semicarbazide is used in the formulation of various chemical reagents, which are essential in a wide range of chemical analyses and laboratory procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 3839-82-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3839-82:
(6*3)+(5*8)+(4*3)+(3*9)+(2*8)+(1*2)=115
115 % 10 = 5
So 3839-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O/c11-10(14)13-12-8-4-7-9-5-2-1-3-6-9/h1-8H,(H3,11,13,14)
3839-82-5Relevant articles and documents
Green and Facile Synthesis of New 3-(Phenylallylideneamino)indeno[1,2-d]imidazoles
Ghalib
, p. 412 - 414 (2019)
A green and facile strategy has been proposed for the synthesis of previously unknown 3a,8a-dihydroxy-3-[(3-phenylprop-2-en-1-ylidene)amino]-2-sulfanylidene-2,3,3a,8a-tetrahydro-1H-indeno[1,2-{und}]imidazol-8-one and 3a,8a-dihydroxy-3-[(3-phenylprop-2-en-
Chemoselective preparation of oximes, semicarbazones, and tosylhydrazones without catalyst and solvent
Bandgar, Babasaheb P.,Sadavarte, Vaibhav S.,Uppalla, Lav S.,Govande, Rahul
, p. 403 - 406 (2007/10/03)
A simple and versatile method for the synthesis of oximes, semicarbazones, and tosylhydrazones of aldehydes in the presence of ketones without catalyst and solvent is presented.
