نتایج جستجو برای: methylamino pyridine

تعداد نتایج: 14475  

2012
Thorben Reinert Inke Jess Christian Näther

The asymmetric unit of the title compound, [Cd(NCS)(2)(C(9)H(13)N)(4)], consists of one Cd(II) cation located on a centre of inversion, one thio-cyanate anion, one 3-tert-butyl-pyridine ligand and one 4-tert-butyl-pyridine ligand in general positions. The tert-butyl group of the 4-tert-butyl-pyridine ligand is disordered over two sets of sites in a 0.25:0.75 ratio and was refined using a split ...

2013
Muhammet Işıklan Ömer Sonkaya Tuncer Hökelek

The title compound, C17H14Cl4N5OP3, is a spiro-phosphazene derivative with bulky naphthalene and pyridine rings. The phosphazene and the six-membered N/O rings are in flattened-boat and twisted-boat conformations, respectively. The naphthalene ring system and the pyridine ring are oriented at a dihedral angle of 18.06 (8)°. In the crystal, weak π-π stacking between the pyridine rings and betwee...

Journal: :Bulletin of The Chemical Society of Ethiopia 2022


 ABSTRACT. A novel series of mononuclear complexes the type, [M(L)(H2O)2] [M = Co(II) (1), Ni(II) (2), Zn(II) (3), Cd(II) (4), L dipicolinate), has been investigated using various techniques, including elemental analyses, FT-IR, 1H- and 13C NMR spectroscopy, powder XRD thermogravimetric analysis. The results indicate that coordination dipicolinic acid to metal ions involves two carboxylat...

Journal: :Journal of The Iranian Chemical Society 2022

Abstract New spiro[cyclohexane-1,2'-thiazolo[4,5- b ]pyridine derivatives ( 3 – 23 ) were investigated. Then there is in vitro antimicrobial potency against possible organisms Staphylococcus aurous ATCC-47,077, Bacillus cereus ATCC-12228, Escherichia coli ATCC-25922, Salmonella typhi ATCC-15566, and Candida albicans ATCC-10231 tested utilizing commercially available antibiotics ampicillin as a ...

Journal: :Cancer research 1954
E V BROWN P L MALLOY P McCARTHY M J VERRETT L R CERECEDO

The first paper of this series (1) reported the results of tests of the carcinogenic activity of cer tam analogs of p-dimethylaminoazobenzene (DAB) in which a pyridine ring or a thiazole ring replaced one of the benzene rings of DAB. Due to the presence of the hetero atom or atoms, position isomers are possible in the heterocyclic analogs, and some of these isomers were synthesized and tested. ...

Journal: :The Journal of biological chemistry 1960
T GRIFFITH K P HELLMAN R U BYERRUM

Dawson et al. (1) have shown that the pyridine ring of nicotinic acid is utilized to form the pyridine ring of nicotine in sterile cultures of tobacco root. Since studies with animals and some microorganisms have demonstrated that tryptophan is converted to nicotinic acid (2)) tryptophan might reasonably be expected to yield the pyridine ring of nicotine. However, experiments have shown conclus...

Journal: :Journal of Supercritical Fluids 2021

Conventional leather dyeing consumes high amounts of dyes and increases pollution tannery wastewater. We have focused on the reduction dyestuff avoidance water additional chemicals for colorization leather. Waterless with supercritical CO2 as solvent dye 1-(methylamino)anthraquinone was performed in a technical scale autoclave. The intensity uniformity dyed leathers assessed using spectroscopic...

Journal: :Acta Crystallographica Section E Structure Reports Online 2008

2011
Fu-Yue Dong Jie Wu Hai-Yan Tian Qing-Mei Ye Ren-Wang Jiang

IN THE TITLE COMPOUND (SYSTENATIC NAME: 3,4,5-trihy-droxy-benzoic acid pyridine monosolvate), C(5)H(5)N·C(7)H(6)O(5), the gallic acid mol-ecule is essentially planar (r.m.s deviation = 0.0766 Å for non-H atoms) and is linked to the pyridine mol-ecule by an O-H⋯N hydrogen bond. An intra-molecular O-H⋯O hydrogen bond occurs in the gallic acid mol-ecule. The gallic acid and pyridine mean planes ma...

Journal: :The Journal of antibiotics 1997
R Obata T Sunazuka Z Tian H Tomoda Y Harigaya S Omura

Structure-activity relationships of the pyridine-pyrone moiety in pyripyropene A (1), a potent acyl-CoA: cholesterol acyltransferase (ACAT) inhibitor of fungal origin, were studied. Several kinds of aromatic or hetero ring substituents for the pyridine moiety were synthesized using unique degradation reaction, following by gamma-acylation. All the six synthesized analogs decreased the inhibitor...

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