Aldehydes

<p>1,5-Dimethyl-1H-indole-3-carbaldehyde is a useful building block for organic synthesis. It is an important reagent for the synthesis of complex compounds and it has been used as a versatile building block in organic chemistry. This compound can be used as a starting point for the preparation of other chemicals, such as pharmaceuticals, pesticides, and dyes. 1,5-Dimethyl-1H-indole-3-carbaldehyde is also a fine chemical that has been used for research purposes. There are no known commercial uses for this compound.</p>

<p>3-Butoxybenzaldehyde is an electron donor. It is used in the synthesis of heterocyclic compounds and as a reagent or postulated intermediate in the formation of epoxides, ethylene, and peroxides. 3-Butoxybenzaldehyde also functions as a precursor to other oxygenated compounds. 3-Butoxybenzaldehyde has been shown to undergo both aldol condensation and interaction with other compounds.</p>

<p>2-Bromo-3,6-difluorobenzaldehyde is a versatile building block that is used in the synthesis of many complex compounds. It has been shown to be a useful intermediate and reaction component in organic synthesis. 2-Bromo-3,6-difluorobenzaldehyde can be used as a reagent or speciality chemical for research purposes. This compound has high quality and is a useful scaffold for the preparation of fine chemicals.</p>

<p>Intermediate in the synthesis of ipragliflozin</p>

<p>5-Hydroxy-4-methoxy-2-nitrobenzaldehyde is a substrate molecule that can be minimised to the corresponding oxime, which can then be oxidised to form an aldehyde. The product of this reaction is a conformationally restricted dienone. This compound has been synthesized using a number of different methods, including oxidation by sodium dichromate. 5-Hydroxy-4-methoxy-2-nitrobenzaldehyde is a phenolic compound with two aromatic rings and one carbon ring. It has natural product properties and is used as a chemical skeleton in the synthesis of other compounds.</p>

<p>6-Fluorosalicylaldehyde is a sulfate that has been used in the synthesis of 6-fluorosalicylic acid, which is an intermediate for the production of aspirin. It also can be used to synthesize phenols and formylation products. The reaction with hydroxylamine leads to salicylaldehydes, while the reaction with methoxide leads to salicylaldehyde.<br>6-Fluorosalicylaldehyde reacts with magnesium salts in acidic conditions to produce paraformaldehyde. Deprotonation of 6-fluorosalicylaldehyde yields methoxide.</p>

<p>2,5-Dibromobenzaldehyde is a synthetic compound that has been shown to have a red fluorescent emission. It is also thermally stable and can be used in the synthesis of quinoline derivatives. 2,5-Dibromobenzaldehyde may be used as a potential fluorescent label for viologen or amines. This compound can undergo an intermolecular Diels-Alder reaction with diacetate to form a bicyclic system, which is important to the understanding of its interactions with other compounds.</p>

<p>5-Fluoro-1-Methyl-1H-Indole-3-Carbaldehyde is a high quality chemical that is used as a reagent, an intermediate for the synthesis of pharmaceuticals, and in the production of fine chemicals. 5FMICA is also a useful scaffold for developing valuable building blocks. This chemical has been shown to be a versatile building block for the synthesis of complex compounds. 5FMICA can be used as a reaction component for the preparation of speciality chemicals and research chemicals.</p>

<p>8-Hydroxy-5-nitroquinoline-2-carbaldehyde is a high quality, versatile building block that can be used as a reaction intermediate or to synthesize heterocycles. It is also a useful scaffold for the synthesis of complex compounds. The CAS number of this chemical is 884497-63-6.</p>

<p>5-Methoxy-1-methyl-1H-indole-3-carbaldehyde is a synthetic compound that has been shown to inhibit the growth of human tumour cells in vitro. This compound is a regioisomeric mixture of two enantiomers, with the (S) isomer being the more potent inhibitor. The (R) isomer was found to be less active against human tumour cells and may have an antimicrobial activity. 5-Methoxy-1-methyl-1H-indole-3-carbaldehyde has been shown to be bioreductive towards electron donors such as NADPH and glutathione. It also inhibits dt diaphorase and aerobic metabolism in human tumour cells.</p>

<p>4-Methoxy-3,5-dimethyl-2-pyridinecarboxaldehyde is a trifunctional molecule that has been shown to suppress the growth of cancer cells in mice. This compound is an inhibitor of acid synthesis and has also been shown to be an antirheumatic drug. 4-Methoxy-3,5-dimethyl-2-pyridinecarboxaldehyde inhibits the activity of three enzymes: synthetase, an enzyme that synthesizes fatty acids; 3-ketoacyl CoA synthase, which synthesizes ketones; and enoyl CoA reductase, which produces fatty acids. The long term efficacy of this molecule has not yet been studied in humans.</p>

<p>5-Chloro-2-methoxybenzaldehyde is a potent inhibitor of the bacterial enzyme acetylcholinesterase. It has been shown to have an interaction with biomolecules, such as chalcones, and can be used in the manufacture of antibacterial agents. 5-Chloro-2-methoxybenzaldehyde has been found to have potent inhibitory activity against organocatalytic aldehydes and atypical aldehydes and can be used as an active ingredient in the synthesis of novel compounds with antibacterial activity.</p>

<p>3-Allyl salicylaldehyde is a fluorescent probe that is used to measure the mitochondrial membrane potential. It can be used as an amine-reactive fluorescence probe for the detection of amines such as histamine and serotonin. 3-Allyl salicylaldehyde has been shown to bind to metal complexes, such as palladium complexes, immobilized on silica gel. The cavity of the immobilized metal complex acts as an adsorption site for 3-allyl salicylaldehyde, which binds to the cavity by means of a metal chelate mechanism. This binding results in an alteration in the absorption spectra and x-ray absorption properties of 3-allyl salicylaldehyde. The hydroxyl group of 3-allyl salicylaldehyde is not involved in this binding process with the immobilized metal complex, while its carbonyl group is important for this interaction.</p>

<p>2,5-Dimethoxyterephthalaldehyde (2,5DMP) is a protonated molecule that can be used in sample preparation for analytical methods. 2,5DMP has been used as a dispersive solid-phase extraction solvent and an adsorbent material. This compound has been shown to exhibit strong hydrophobic interactions with the carbonyl group of aromatic compounds and to have a high chemical stability. 2,5DMP also has an electrochemical impedance spectroscopy (EIS) property that can be used for monitoring the electrochemical behaviour of molecules and magnetic particles in the solution. The EIS property has been enhanced by hydrogen bonding between the protonated molecules and metal ions in the solution.</p>

<p>4'-Methyl-2,2'-bipyridine-4-carboxaldehyde is a heterocyclic compound that contains a nitro group. It has the chemical formula C8H6N2O and the molecular weight of 122.15 g/mol. This compound belongs to the class of formyl compounds and it is composed of two formyl groups and one hydrogen atom. The bipyridines are linked by a methylene bridge to form a six-membered ring. The compound can be used as an intermediate for the synthesis of other organic compounds such as pharmaceuticals, dyes, water repellents, pesticides, and herbicides.</p>

<p>2,5-Dibromoterephthalaldehyde is a red fluorescent compound that has been shown to have potential as a cancer therapy. The compound is able to bind to the electron acceptor 2,5-dibromoterephthalate (DBT) and can be used in photocatalytic reactions. It has been shown that 2,5-dibromoterephthalaldehyde can cause high levels of cell death in cancer cells with low levels of toxicity to healthy cells. This property may be due to its ability to target cancerous cells by binding with their mitochondria. The compound is also fluorescent and emits light when excited with UV light. 2,5-Dibromoterephthalaldehyde has been shown to form structured metallacycles in the presence of copper ions.<br>!--</p>

<p>2-(4-Methoxyphenoxy)benzaldehyde is a fine chemical that is used as a versatile building block in the synthesis of complex compounds and research chemicals. 2-(4-Methoxyphenoxy)benzaldehyde is also a reagent that can be used to synthesize speciality chemicals, useful building blocks, and reaction components. This chemical may be used as an intermediate for the synthesis of high-quality pharmaceuticals or other useful scaffolds. It has CAS number 19434-36-7.</p>

<p>2-Hydroxy-4,6-dimethoxy-3,5-dimethylbenzaldehyde is a versatile building block that can be used in research chemicals, reagents, and speciality chemicals. It is also a useful building block that can be used as a reaction component or scaffold for high-quality compounds. This chemical has been shown to have antihistamine properties with applications in treatment of allergies and asthma.</p>

<p>4-Hydroxy-2-iodobenzaldehyde is a high quality chemical that belongs to the group of complex compounds. It has been shown to be a useful intermediate, fine chemical, and speciality chemical. It can also be used as a reaction component in the synthesis of other chemicals and is an important building block for making other compounds. 4-Hydoxy-2-iodobenzaldehyde is versatile and can be used in many different reactions.</p>

<p>3-Ethynylbenzaldehyde is a tryptic, nitro compound that contains terminal alkynes and has functional groups. The functional theory of this compound suggests that it may be used as a chemosensor for the detection of acidic compounds. 3-Ethynylbenzaldehyde reacts with sodium trifluoroacetate to form an aldehyde, which is then oxidized to an acid by the addition of water. This acid can be detected using NMR spectroscopy. 3-Ethynylbenzaldehyde has been shown to react with sodium trifluoroacetate in solid form at room temperature and above. The resulting product is a yellow crystalline solid that can be identified by its UV spectrum.</p>

<p>3-Bromothiophene-2-carbaldehyde is an organic compound that has been shown to have antibacterial activity. It can be synthesized by reacting triethyl orthoformate with methyl ketones in the presence of a photocatalyst such as titanium dioxide or zinc oxide. This reaction produces 3-bromothiophene-2-carboxylic acid which reacts with ammonia and hydrogen bromide to form 3-bromothiophene-2-carbaldehyde. 3-Bromothiophene-2-carbaldehyde has been shown to inhibit the growth of cancer cells and induce apoptosis, which may be due to its ability to inhibit angiogenesis. The anticancer properties are most likely due to its ability to bind DNA and inhibit protein synthesis, leading to cell death.</p>

<p>2-Hydroxy-5-methylisophthalaldehyde is a tetranuclear coordination compound with a tridentate ligand. The ligand can bind to three metal ions in the same way as an octahedral geometry, but the fourth nitrogen atom is not coordinated and can be replaced by other ligands. Two of these compounds have been synthesized and their structures determined by x-ray crystallography. The ligands are planar and form hydrogen bonds, which contribute to the high stability of these compounds. These properties may be useful for biological studies, such as synchronous fluorescence and intramolecular hydrogen transfer, as well as for catalysis and chemical sensing.</p>