Results 1 to 10 of about 70,928 (193)

The Effect of Hydrogen Bonding and Azomethine Group Orientation on Liquid Crystal Properties in Benzylidene Aniline Compounds

open access: yesActa Chimica Slovenica, 2020
This study examines the effects of substituents and hydrogen bonding, orientations of imine linkage on the behavior of benzylidene aniline compounds as liquid crystals (LC).
Abdullah Hussein Kshash
doaj   +1 more source

Synthesis, Characterization and Evaluation Antibacterial Activity of Some Schiff Bases and (1,3-Oxazepine or Diazepine-4,7-Dione) [PDF]

open access: yesKirkuk Journal of Science, 2019
In this study, some of Schiff bases, 1,3-oxazepine-4,7-dione and 1,3-diazepine-4,7-dione compounds derived from terephthalaldehyde and substituted aniline have been prepared, Schiff bases (a1-5) which derived from terephthalaldehyde and substituted ...
Saad Jasim
doaj   +1 more source

Using of Acetylacetone-formaldehyde Reagent in Spectrophotometric Determination of Aniline in Various Water Samples [PDF]

open access: yesمجلة التربية والعلم, 2020
A simple and accurate spectrophotometric method for the estimation of aniline in various water samples was done. The method was based on the condensation reaction of acetyl acetone-formaldehyde(AC-FA) reagent with aniline.
Nabeel Othman   +3 more
doaj   +1 more source

The removal efficiencies and mechanism of aniline degradation by peroxydisulfate activated with magnetic Fe-Mn oxides composite

open access: yesWater Reuse, 2021
The Fe-Mn oxides composite prepared by a chemical co-precipitation method was used as a heterogenous peroxydisulfate catalyst for the decomposition of aniline.
Lin Qiao   +4 more
doaj   +1 more source

3D-printed devices for continuous-flow organic chemistry [PDF]

open access: yes, 2013
We present a study in which the versatility of 3D-printing is combined with the processing advantages of flow chemistry for the synthesis of organic compounds.
Cronin, Leroy   +4 more
core   +6 more sources

An efficient synthesis of furan-3(2H)-imine scaffold from alkynones

open access: yesRoyal Society Open Science, 2021
A novel efficient method to generate spiro furan-3(2H)-imine derivatives is established by the reaction between the α,β-unsaturated ketones and aniline derivatives.
Anas J. Rasras   +4 more
doaj   +1 more source

Data on synthesis and characterization of new p-nitro stilbene Schiff bases derivatives as an electrochemical DNA potential spacer

open access: yesData in Brief, 2020
The structural investigation of synthesized compounds can be carried out by various spectroscopic techniques. It is an important prospect in order to elucidate the structure of the desired products before being further utilized.
Nur Zafirah Mohd Izham   +9 more
doaj   +1 more source

Inclusion compounds of isomeric xanthenol hosts with aniline [PDF]

open access: yesActa Crystallographica Section A Foundations of Crystallography, 2005
Two isomeric xanthenol host compounds have been found to form inclusion compounds with aniline (ANI). These hosts are H1 = 9-(4-methoxyphenyl)-9H-xanthen-9-ol and H2 = 9-(3-methoxyphenyl)-9H-xanthen-9-ol. We have elucidated the structures of the inclusion compounds and determined their kinetics of desolvation.
Ayesha Jacobs   +2 more
openaire   +1 more source

Synthesis of N1-(3,5-Bis(trifluoromethyl)benzyl)benzene-1,2-diamine and N,N-Bis(2-nitrophenyl)-3,5-bis(trifluoromethyl)aniline

open access: yesMolbank, 2023
A monosubstituted benzene-1,2-diamine building block, N1-(3,5-bis(trifluoromethyl)benzyl)benzene-1,2-diamine, was prepared in two steps from commercially available 3,5-bis(trifluoromethyl)benzylamine and 1-fluoro-2-nitrobenzene, while the use of 3,5-bis ...
Luka Ciber   +5 more
doaj   +1 more source

Synthesis and Quantitative Structure–Activity Relationship of Imidazotetrazine Prodrugs with Activity Independent of O6-Methylguanine-DNA-methyltransferase, DNA Mismatch Repair and p53. [PDF]

open access: yes, 2013
The antitumor prodrug Temozolomide is compromised by its dependence for activity on DNA mismatch repair (MMR) and the repair of the chemosensitive DNA lesion, O6-methylguanine (O6-MeG), by O6-methylguanine-DNA-methyltransferase (EC 2.1.1.63, MGMT). Tumor
Arris C. E.   +42 more
core   +1 more source

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