Synthesis, crystal structure and Hirshfeld surface analysis of a new copper(II) complex based on diethyl 2,2'-(4H-1,2,4-triazole-3,5-di-yl)di-acetate. [PDF]
Acta Crystallogr E Crystallogr CommunVynohradov OS +6 more
europepmc +1 more source
(E)-1-(3-(3-Hydroxy-4-Methoxyphenyl)-1-(3,4,5-Trimethoxyphenyl)allyl)-1H-1,2,4-Triazole and Related Compounds: Their Synthesis and Biological Evaluation as Novel Antimitotic Agents Targeting Breast Cancer. [PDF]
Pharmaceuticals (Basel)Ana G +8 more
europepmc +1 more source
Related searches:
Strategies for synthesis of 1,2,4-triazole-containing scaffolds using 3-amino-1,2,4-triazole
Molecular Diversity, 20211,2,4-Triazole-containing scaffolds are unique heterocyclic compounds present in an array of pharmaceuticals and biologically important compounds used in the drug-discovery studies against cancer cells, microbes, and various types of disease in the human body.
Shima Nasri +2 more
openaire +2 more sources
Mass spectra of 1,2,4‐triazoles—II: Alkyl 1,2,4‐triazoles
Organic Mass Spectrometry, 1973AbstractThe mass spectra of monomethyl 1,2,4‐triazoles contain fragment ions produced by specific cleavage of the heterocyclic ring. A major fragmentation from many molecular ions involves the elimination of HCN, but loss of N2 is either very small or completely absent.
A. J. Blackman, J. H. Bowie
openaire +1 more source
ChemInform Abstract: 1,2,4‐TRIAZOLES. VII. METHYLATION OF 1,2,4‐TRIAZOLES
Chemischer Informationsdienst, 1977AbstractMethylierung von 1,2,4‐Triazol und dessen symmetrisch 3,5‐disubst.
M. UDA, Y. HISAZUMI, K. SATO, S. KUBOTA
openaire +1 more source
Hydroxyphenylazo-1,2,4-triazoles
Australian Journal of Chemistry, 1973Azo dyes have been prepared by coupling phenols with diazotized C- amino-1,2,4-triazole and p-aminophenyl-1,2,4-triazoles. Spectroscopic proofs of structure establish preferential para-coupling. The dyes exist in the azo form without evidence for quinone hydrazone tautomers. Spectroscopic evidence and chelation not involving the phenolic hydroxyl group
JB Polya, M Woodruff
openaire +1 more source
Azinoiminophosphorane Mediated 1,2,4‐Triazole Synthesis.
ChemInform, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Chang Hoon Lee, Kee‐Jung Lee
openaire +1 more source
[288-88-0] C2H3N3 (MW 69.08) InChI = 1S/C2H3N3/c1-3-2-5-4-1/h1-2H,(H,3,4,5) InChIKey = NSPMIYGKQJPBQR-UHFFFAOYSA-N (transacylating agent used for ester and amide synthesis, especially in peptide synthesis; cyclization reactions; oligonucleotide synthesis) Physical Data: mp 120–121 °C; bp 260 °C (dec above 187 °C); fp 140
Jean-Claude Gesquière +1 more
openaire +1 more source
This chapter provides a critical update on developments in the chemistry of 1,2,4-triazoles over the last decade. 1,2,4-Triazoles have remained the topic of much research, primarily due to their ubiquitous presence in many pharmaceutical agents and, more recently, in other functional materials with uses in engineering as corrosion inhibitors and in ...
A.D.M. Curtis, N. Jennings
openaire +1 more source
Rearrangement of N-nitro-1,2,4-triazoles into 3-nitro-1,2,4-triazoles
Journal of the Chemical Society, Chemical Communications, 1972Syntheses of the N-nitro-1,2,4-triazoles (1) and (2) and their thermal isomerization into the 3-nitroderivatives (3) and (4) is described; this thermal rearrangement of N-nitro-azoles to their corresponding C-nitro-compounds is suggested to be an example of a [1,5] sigmatropic shift of the NO2 group.
Clarisse L. Habraken +1 more
openaire +1 more source