4949-24-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 15 carbon (C) atoms, 13 hydrogen (H) atoms, and 5 nitrogen (N) atoms.
Explanation
Triazole compounds are a class of organic compounds characterized by a five-membered ring containing three nitrogen atoms. This specific compound belongs to this class.
Explanation
The compound is unique because it has two phenyl groups (C6H5) attached to the nitrogen atoms at positions 1 and 5 on the triazole ring, which differentiates it from other triazole compounds.
Explanation
The compound is used in the synthesis of various pharmaceuticals, indicating its importance in the development of new drugs.
Explanation
The compound can act as a ligand, which is a molecule that donates one or more electrons to a central atom to form a coordination complex. This property makes it useful in coordination chemistry.
Explanation
Due to its structural and functional properties, the compound has potential applications in medicinal chemistry for the development of new drugs and in material science for the creation of new materials with specific properties.
Explanation
The compound is classified as an organic compound because it contains carbon and hydrogen atoms, along with other elements like nitrogen in its structure.
Class
Triazole compounds
Unique feature
Two phenyl groups attached to nitrogen atoms at positions 1 and 5
Application
Synthesis of pharmaceuticals
Role
Ligand in coordination chemistry
Potential applications
Medicinal chemistry and material science
Organic compound
Yes
Check Digit Verification of cas no
The CAS Registry Mumber 4949-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4949-24:
(6*4)+(5*9)+(4*4)+(3*9)+(2*2)+(1*4)=120
120 % 10 = 0
So 4949-24-0 is a valid CAS Registry Number.
4949-24-0Relevant articles and documents
Synthesis and biological evaluation of 3-amino-1,2,4-triazole derivatives as potential anticancer compounds
Benhida, Rachid,Demange, Luc,Dufies, Maeva,Grytsai, Oleksandr,Hagege, Anais,Martial, Sonia,Pagès, Gilles,Penco-Campillo, Manon,Ronco, Cyril,Valiashko, Oksana
, (2020/10/02)
Two series of compounds carrying 3-amino-1,2,4-triazole scaffold were synthesized and evaluated for their anticancer activity against a panel of cancer cell lines using XTT assay. The 1,2,4-triazole synthesis was revisited for the first series of pyridyl derivatives. The biological results revealed the efficiency of the 3-amino-1,2,4-triazole core that could not be replaced and a clear beneficial effect of a 3-bromophenylamino moiety in position 3 of the triazole for both series (compounds 2.6 and 4.6) on several cell lines tested. Moreover, our results point out an antiangiogenic activity of these compounds. Overall, the 5-aryl-3-phenylamino-1,2,4-triazole structure has promising dual anticancer activity.
A convenient and efficient method for the synthesis of mono- and N,N-disubstituted thioureas
Kodomari, Mitsuo,Suzuki, Masato,Tanigawa, Keiko,Aoyama, Tadashi
, p. 5841 - 5843 (2007/10/03)
A convenient method for the synthesis of mono- and N,N-disubstituted thioureas by the debenzoylation of N-substituted- and N,N-disubstituted- N′-benzoylthioureas with hydrazine hydrate under solvent-free conditions has been developed. N-Substituted-N′-benzoylthioureas and hydrazine hydrate were mixed, and stirred at room temperature without a solvent to give the corresponding N-substituted thioureas in high yields.
