Ethylamines - Open Access .click

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Spectroscopic studies of the molecular interactions in n-ethylamines and 2-nitropropane/n-ethylamine mixtures

Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2004
New experimental results are reported on molecular interactions in the n-ethylamines and 2-nitropropane (2-NP)/n-ethylamine mixtures studied by Raman spectroscopy under pressure in a diamond anvil cell (0-50 GPa) and, at ambient pressure, by infrared spectroscopy.
Cédric, Gobin +2 more
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Utilization of ethylamine by yeasts

Antonie van Leeuwenhoek, 1962
Thirty-two yeast species (162 strains) have been examined for their ability to utilize ethylamine hydrochloride as sole source of nitrogen. The possible taxonomic use of this property is discussed. The utilization of ethylamine was, with one exception, found to coincide with an ability to utilize L(+)-lysine.
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Microwave spectrum of ethylamine-gauche

Journal of Molecular Structure, 1983
Abstract The gauche rotamer of the ethylamine molecule was successfully assigned making ample use of MW-MW-DR-techniques. The transitions of the gauche form appear as quartets due to two large amplitude motions: the CN torsion and inversion. The rotational as well as interaction constants for all four states were fitted as well as their relative ...
E. Fischer, I. Botskor
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The action of ethylamine on cellulose part I—The acetylation of ethylamine-treated cotton

Polymer, 1962
Abstract The hygroscopicity of cotton that has been acetylated in pyridine after it has been treated with ethylamine, washed with water, and solvent-exchanged with pyridine, has been compared with that of cotton acetylated without pretreatment. The results show that the acetylation does not cause decrystallization additional to that due to the ...
T NEVELL, S ZERONIAN
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Heterocyclic cycloalkanol ethylamines as norepinephrine reuptake inhibitors

Bioorganic & Medicinal Chemistry Letters, 2010
A series of heterocyclic cycloalkanol ethylamines have been prepared to expand our norepinephrine reuptake inhibitor (NRI) program. Synthesis of a variety of heterocycles identified (+)-S-21, a potent NRI efficacious in an animal model for thermoregulatory dysfunction.
Joseph P, Sabatucci +9 more
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Tea as a Source of Urinary Ethylamine

Nature, 1966
ETHYLAMINE is a normal constituent of human urine1,2, but it is not found in rat urine. This suggested that urinary ethylamine might be a product of metabolism of a component of food or beverages.
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N-(4-Pyrimidyl)ethylamine derivatives

Chemistry of Heterocyclic Compounds, 1970
In order to find antitumoral agents, a number of new N-(4-pyrimidyl) ethylamine derivatives have been synthesized from 4,6-dichloropyrimidine, 6-amino-4-chloropyrimidine, 4-chloro-6-hydroxypyrimidine, and various ethylamines substituted in theΒ position.
V. N. Sokolova, O. Yu. Magidson
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Conformational behaviour of fluorinated ethylamines

Journal of Molecular Structure, 1984
Abstract The infrared and Raman spectra of various flourinated ethylamines have been obtained for different phases. Emphasis has been put on the conformational behaviour in inert gas matrices. Some preliminary results for 2-fluoroethylamine and 2,2,2-trifluoroethylamine are given in the present communication.
G.O. Braathen, A. Lautie
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Ethylamine

2023
Philip H. Howard +3 more
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1-(1-Naphthyl)ethylamine

2001
(±) [42882-31-5] C12H13N (MW 171.26) InChI = 1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3 InChIKey = RTCUCQWIICFPOD-UHFFFAOYSA-N (+) [3886-70-2] InChI = 1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3/t9-/m1/s1 InChIKey = RTCUCQWIICFPOD-SECBINFHSA-N (−) [10420-89-0] InChI = 1S/C12H13N/c1-9(13)11-
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