10480-11-2 Usage
Uses
Used in Pharmaceutical Research and Development:
1-(4-nitrophenyl)-5-phenyl-4,5-dihydrotriazole is used as a chemical intermediate for the synthesis of new drugs, leveraging its unique structural features to contribute to the development of innovative pharmaceutical compounds.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-nitrophenyl)-5-phenyl-4,5-dihydrotriazole is employed as a key building block, facilitating the creation of complex organic molecules and contributing to the advancement of synthetic chemistry.
Used in Agricultural Chemicals:
1-(4-nitrophenyl)-5-phenyl-4,5-dihydrotriazole may be utilized as a component in the formulation of agricultural chemicals, potentially enhancing the effectiveness of pesticides or other agrochemicals through its chemical properties.
Used in Materials Science:
In materials science, 1-(4-nitrophenyl)-5-phenyl-4,5-dihydrotriazole could be explored for its potential to improve or create new materials with specific properties, such as in the development of high-performance polymers or other advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 10480-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10480-11:
(7*1)+(6*0)+(5*4)+(4*8)+(3*0)+(2*1)+(1*1)=62
62 % 10 = 2
So 10480-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N4O2/c19-18(20)13-8-6-12(7-9-13)17-14(10-15-16-17)11-4-2-1-3-5-11/h1-9,14H,10H2
10480-11-2Relevant academic research and scientific papers
Metal-Free 1,2,3-Triazole Synthesis in Deep Eutectic Solvents
Díez-González, Silvia,Haselgrove, Samuel,Sebest, Filip,White, Andrew J. P.
supporting information, p. 605 - 609 (2020/04/08)
The metal-free regioselective preparation of 1,5- and 1,4-disubstituted triazoles is reported through a cycloaddition-elimination sequence. Reactions were carried out in environmentally friendly deep eutectic solvent (DES) and pure products were isolated
Thermal azide-Alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-Triazolines in deep eutectic solvents
Sebest, Filip,Casarrubios, Luis,Rzepa, Henry S.,White, Andrew J. P.,Díez-González, Silvia
supporting information, p. 4023 - 4035 (2018/09/11)
The multi-gram synthesis of a wide range of 1,2,3-Triazolines via azide-Alkene cycloaddition reactions in a Deep Eutectic Solvent (DES) is reported. The role of DES in this transformation as well as the origin of the full product distribution was studied with an experimental/computational-DFT approach.
Triazolines. XXXIX. 1,5-Diaryl-δ2-1,2,3-triazolines as Aphicides: Mechanism of Action via Aziridine Formation
Kadaba, Pankaja K.
, p. 299 - 304 (2007/10/03)
The aphicidal activity of 21 different 1,5-diphenyl-Δ2-1,2,3-triazolines, conveniently prepared utilizing the catalytic effect of water on the 1,3-cycloaddition of diazomethane to Shiff bases in aqueous dioxane, was evaluated. Triazolines beari
