Aldehydes

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5-Oxazolecarboxaldehyde is a supramolecular compound that is used in the detection of biomolecules. It has been used to synthesize phorboxazole, which is an antifungal agent. 5-Oxazolecarboxaldehyde has also been shown to be an antibacterial and antifungal agent. 5-Oxazolecarboxaldehyde can be detected using luminescent probes or analytical methods such as gas chromatography and mass spectrometry.

1-Ethyl-1H-indole-3-carbaldehyde is a potent anticancer agent that belongs to the group of anions. It can be used in the treatment of cancer, with potent anticancer activity against a number of human cancer cells. 1-Ethyl-1H-indole-3-carbaldehyde has been shown to effectively inhibit DNA replication and induce DNA strand breaks. It also has chemosensory properties, which make it an ideal candidate for use as a sensor molecule. This compound is capable of binding to methylene groups on proteins and may interfere with the function of these molecules, which are involved in cell division. 1-Ethyl-1H-indole-3-carbaldehyde also exhibits strong vibrational and optical properties; it absorbs strongly in the ultraviolet region (280 nm) and has a low extinction coefficient at 400 nm. Its absorption spectrum extends into the visible region as well, where it exhibits intense coloration.

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Applications 5-Bromo-2-thiophenecarboxaldehyde is used in biological studies as anti-inflammatory and anti-tumor activity of the marine mangrove Rhizophora apiculata. References Prabhu, V.V., et al.: J. Immunotoxicol., 9, 341 (2012);

1H-Indazole-6-carbaldehyde is a fluorescent molecule that exhibits chemosensors and electrochemiluminescence properties. It has been shown to interact with molecular probes, such as dopamine and metal ions, indicating that it may also have an antiarrhythmic effect. The nature of the fluorescence emission is still not fully understood, but it is postulated to be due to a hydrogen bond between the imine group and the carbonyl group. 1H-Indazole-6-carbaldehyde has been used in luminescent materials for postcards and advertisements, which are popular in Japan.

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4,6-Dimethoxysalicylaldehyde is a protonated molecule with a cyclohexane ring and 4 hydroxyl groups. Its chemical formula is C6H8O3. The compound has low bioavailability due to the presence of an intramolecular hydrogen bond that causes high redox potential. There are two amines on the aromatic ring which can coordinate with metal ions to form a complex. This compound's structural analysis has been conducted using X-ray crystallography, NMR spectroscopy, and IR spectroscopy. The structure of 4,6-dimethoxysalicylaldehyde is unsymmetrical due to the presence of two asymmetric carbon atoms in the molecule. It forms hydrogen bonds with other molecules due to its hydroxyl group and intramolecular hydrogen bond. Hydrogen bonding interactions occur between this compound and other molecules including water, alcohols, ammonia, amines, and carboxylic acids.

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2,5-Dimethylbenzaldehyde is a chemical compound that belongs to the group of fatty acid esters. It is an aromatic compound that has a pleasant, nutty odor. 2,5-Dimethylbenzaldehyde can be found as a byproduct in the production of diethyl succinate from ethyl benzene. It is also present in the emissions of 3,4-dimethylbenzyl alcohol and can be found in model systems for proton transfer reactions. The Gattermann-Koch reaction was developed for the synthesis of 2,5-dimethylbenzaldehyde. This chemical can be synthesized by reacting benzoic acid with dimethylether and thermodynamic data are available for this reaction mechanism. Chemical ionization mass spectroscopy can be used to identify this chemical in fatty acids.

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