59401-82-0 Usage
Aromatic aldehyde
It is a compound with an aromatic ring system that includes a conjugated system of double bonds and delocalized electrons, contributing to its stability and distinct chemical properties.
Phenyl group attachment
A phenyl group (a ring of 6 carbon atoms with a lone pair of electrons on each carbon) is attached to the 1,2,3-triazole ring, which influences the compound's reactivity and stability.
1,2,3-Triazole ring
A 5-membered heterocyclic ring consisting of 2 carbon atoms and 3 nitrogen atoms, which is a key structural component of the compound and contributes to its chemical properties.
Commonly used in organic synthesis
The compound serves as an intermediate or building block in the creation of more complex organic molecules, making it a valuable reagent in the field of organic chemistry.
Wide range of applications
1-phenyl-1,2,3-triazole-5-carbaldehyde is utilized in various industries, such as pharmaceuticals, agrochemicals, and materials science, due to its unique chemical structure and properties.
Building block for synthesis
The compound acts as a starting material or intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other materials, making it an essential component in these industries.
Development of fluorescent probes
1-phenyl-1,2,3-triazole-5-carbaldehyde is used in the development of fluorescent probes for bioimaging, which can help visualize and study biological processes at the molecular level.
Ligand in coordination chemistry
The compound can act as a ligand, binding to metal ions to form coordination complexes with potential applications in catalysis, materials science, and other areas.
Antimicrobial potential
Studies have shown that 1-phenyl-1,2,3-triazole-5-carbaldehyde possesses antimicrobial properties, making it a potential candidate for the development of new antimicrobial agents.
Anticancer properties
Research has indicated that the compound may have anticancer properties, highlighting its potential as a therapeutic agent in cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 59401-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,0 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59401-82:
(7*5)+(6*9)+(5*4)+(4*0)+(3*1)+(2*8)+(1*2)=130
130 % 10 = 0
So 59401-82-0 is a valid CAS Registry Number.
59401-82-0Relevant academic research and scientific papers
Azide cyclizations with acetylenic silyl ketone: a general access to functionalized-1,2,3-triazolylacylsilanes and aldehydes
Degl'Innocenti, Alessandro,Scafato, Patrizia,Capperucci, Antonella,Bartoletti, Laura,Mordini, Alessandro,Reginato, Gianna
, p. 9031 - 9034 (2007/10/02)
Reaction of several azido compounds with acetylenic silyl ketone affords a simple and direct entry to triazolylacylsilanes and, after desilylation, to the corresponding functionalized triazolylaldehydes.
Molecular Rearrangements of 4-Iminomethyl-1,2,3-Triazoles. Replacement of 1-Aryl Substituents in 1H-1,2,3-Triazole-4-carbaldehydes
L'abbe, Gerrit,Bruynseels, Maria,Delbeke, Pieter,Toppet, Suzanne
, p. 2021 - 2027 (2007/10/02)
The two structural isomers, 4 and 5, of 1-substituted-4-iminomethyl-1,2,3-triazoles are interconvertible when heated in dimethyl sulfoxide at 80 deg C.The equilibrium position depends on the electronic properties of the R-substituent, favoring 5 for R = alkyl, benzyl and anisyl, and 4 for p-chlorophenyl and p-nitrophenyl.An interesting application is the synthesis of 1-alkyl-1,2,3-triazole-4-carbaldehydes from 1-phenyl-1,2,3-triazole-4-carbaldehyde by Scheme I.The hydrazones 4i, j and the oxime 4k do not rearrange due to an unfavorable Z-configuration around the C=N bond, whereas the acyloximino derivative 4m is converted into the nitrile 11.The structures of the products have been fully characterized by 13C nmr spectroscopy and the mechanistic details of the rearrangement are discussed.
