16759-44-7 Usage
Five-membered heterocyclic compound
The triazole ring in 1H-1,2,4-Triazole, 1,3,5-trimethyl- consists of five atoms, with three of them being nitrogen atoms.
Three methyl groups
1H-1,2,4-Triazole, 1,3,5-trimethyl- has three methyl groups attached to specific positions on the triazole ring, which distinguishes it from other triazole derivatives.
Potential applications
1H-1,2,4-Triazole, 1,3,5-trimethylhas a variety of potential uses in different fields, such as pharmaceuticals, agriculture, and materials science.
Ligands in coordination chemistry
The compound can serve as a ligand in coordination chemistry, which means it can bind to metal ions to form coordination compounds.
Synthesis of biologically active compounds
1H-1,2,4-Triazole, 1,3,5-trimethylcan be used in the synthesis of various biologically active compounds, which are compounds that have an effect on biological systems.
Corrosion inhibitor
The compound has potential as a corrosion inhibitor in industrial processes, which means it can be used to prevent or slow down the corrosion of materials.
Check Digit Verification of cas no
The CAS Registry Mumber 16759-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,5 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16759-44:
(7*1)+(6*6)+(5*7)+(4*5)+(3*9)+(2*4)+(1*4)=137
137 % 10 = 7
So 16759-44-7 is a valid CAS Registry Number.
16759-44-7Relevant academic research and scientific papers
Photochemistry of N-(Benzoylimino)-1,2,4-triazolium and N-(Benzoylimino)pyridinium Ylides: A Source of Benzoylnitrene Useful in Photolabeling and Photo-Cross-Linking Experiments
Arnold, Charles R.,Melvin, Tracy,Nelson, William M.,Schuster, Gary B.
, p. 3316 - 3319 (2007/10/02)
The photochemistry of substituted 1-(benzoylimino)pyridinium and 4-(N-benzoylimino)-1,2,4-triazolium ylides was investigated to judge their capacity to give aroylnitrenes and their suitability for use in photolabeling experiments.Evidence presented indicates that the triplet states of the ylides cleave to generate aroylnitrenes.In an attempt to enhance triplet formation, nitro- and acetyl-substituted pyridinium ylides were examined.Their irradiation does not give nitrenes in meaningful yield.However, irradiation of the triazolium ylides gives nitrenes in excellent yield.The mechanism of these reactions was probed, and additional evidence is obtained that supports the proposal that benzoylnitrene is a singlet in its ground state.The triazolium ylides may be suitable reagents for photolabeling applications.
