Results 121 to 130 of about 41,815 (148)

Toxicity of 3‐Amino‐1: 2: 4‐Triazole to Activated Sludge Biomass [PDF]

open access: possibleToxicological & Environmental Chemistry, 1984
3‐amino‐1: 2: 4‐triazole (AT), a potent weed killer, added to activated sludge, caused immediate and drastic reduction in oxygen uptake by biomass. AT, a known specific inhibitor of catalases of animal and plant sources, did not appreciably alter catalase of activated sludge biomass.
Cynthia V. Sommer   +2 more
openaire   +1 more source

The preparation of 3:5‐dimethyl‐1‐phenyl‐1:2:4‐triazole [PDF]

open access: possibleJournal of Applied Chemistry, 1952
AbstractOptimum conditions for the laboratory‐scale preparation of 3 : 5‐dimethyl‐1‐phenyl‐1 : 2 : 4‐triazole by the Einhorn‐Brunner method have been studied. The mechanism of the reaction is different from those involved in the triazole syntheses of Pellizzari and Kaiser.
J. B. Polya, A. A. Komzak
openaire   +1 more source

Inhibition of Cholinesterases by 1 : 2 : 4-Triazoles

Nature, 1955
IT has been repeatedly observed in my laboratory that workers, including non-smokers, manipulating 1 : 2 : 4-triazoles develop symptoms of light nicotine or physostigmine poisoning from time to time. Subsequent experiments have shown that some simple water-soluble 1 : 2 : 4-triazoles may act as inhibitors of cholinesterase activity.
openaire   +2 more sources

The preparation of N- and C-halogen derivatives of 1, 2, 4-triazole

Chemistry of Heterocyclic Compounds, 1972
The action of halogens in an alkaline medium on 1, 2, 4-triazoles has given their N-chloro, N-bromo, and N-iodo derivatives. The formation of C-halogen derivatives of some 1, 2, 4-triazoles from their N-halogen derivatives has been studied, and also the action of halogens on 1, 2, 4-triazoles at elevated temperatures.
A. A. Strazdin, V. Ya. Grinshtein
openaire   +2 more sources

Die Röntgenstrukturanalyse von 1, 2, 4‐Triazol

Berichte der Bunsengesellschaft für physikalische Chemie, 1965
AbstractDie Kristallstruktur von 1, 2, 4‐Triazol, C2N3H3, wurde durch dreidimensionale Analyse der Röntgenbeugungsdaten ermittelt. Die Kristalle sind rhombisch (Raumgruppe Pbca‐D152h) mit 8 Molekülen in der Elementarzelle. Die Gitterkonstanten haben die Werte: a = 9,69 ± 0,04 Å, b = 9,38 ± 0,04 Å, c = 7,14 ± 0,03 Å.
openaire   +2 more sources

Synthesis of derivatives of 1, 2, 4-triazole-3, 5-dicarboxylic acid

Chemistry of Heterocyclic Compounds, 1972
By oxidation of 3,5-dimethyl-1,2,4-triazole the monopotassium salt of 1,2,4-triazole-3,5-dicarboxylic acid was obtained. The mononitryl of 1,2,4-triazole-3,5-dicarboxylic acid was isolated during the reaction between 3-diazo-1,2,4-triazole-5-carboxylic acid and potassium cyanide in the presence of copper cyanide.
T. N. Vereshchagina   +3 more
openaire   +2 more sources

1, 2, 4-Triazol-3-one and its nitro and amino derivatives

Chemistry of Heterocyclic Compounds, 1967
Some possible methods of preparation of 1, 2, 4-triazol-3-one are explored. A new method of preparing it from semicarbazide hydrochloride and formic acid is worked out. Nitration of the triazolone gives 5-nitro-1, 2, 3-triazol-3-one, whose structure is proved.
R. P. Bokalder   +2 more
openaire   +2 more sources

A new method of preparing 1, 2, 4-triazole carboxylic-3 acids

Chemistry of Heterocyclic Compounds, 1966
A new convenient method of preparing 1, 2, 4-triazole carboxylic acids-3 is worked out. Aminoguanidine bicarbonate and oxalic acid give 5-amino-1, 2, 4-triazole carboxylic acid-3, and this is converted, via the diazotriazole carboxylic acid and treatment of the latter with methanol, to 1, 2, 4-triazole carboxylic-acid-3.
G. I. Chipen, V. Ya. Grinshtein
openaire   +2 more sources

Insights on the Antioxidant Potential of 1, 2, 4-Triazoles: Synthesis, Screening & QSAR Studies

Current Drug Metabolism, 2014
The aligned manuscript reports synthesis, screening and QSAR analysis of twenty six 1, 2, 4-triazole analogues from their respective aromatic carboxylic acids. The structures of synthesized analogues were characterized using physical and spectral analysis. 1, 2, 4-Triazole analogs antioxidant capacity was determined using DPPH radical scavenging assay.
Rajeev K Singla   +3 more
openaire   +3 more sources

Home - About - Disclaimer - Privacy