Aldehydes

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5-Methoxyindole-3-carboxaldehyde is a molecule that belongs to the genus of indolequinones. It has been shown to have potent inhibitory activity against prostate cancer cells, and also has anti-cancer properties. 5-Methoxyindole-3-carboxaldehyde inhibits the proliferation of cancer cells by inducing apoptosis in prostate cancer cells. 5-Methoxyindole-3-carboxaldehyde also suppresses the growth of cervical cancer cells and breast cancer cells. This molecule binds to the hydrogen bond sites on DNA, which may be one reason for its anti-cancer properties. The molecule is fluorescent and can be used as a marker for detecting cancers or other diseases in living tissue.

4-(4-Fluorobenzyloxy)Benzaldehyde is a macrocycle that has been used as a template for the transformation of various types of molecules. It is an optical theranostic agent, which can be used to monitor photodynamic therapy (PDT). 4-(4-Fluorobenzyloxy)Benzaldehyde has shown toxicities in animals, such as respiratory distress and hepatotoxicity. However, the toxicity is not observed when it is used in low concentrations for PDT. The drug also has luminescence properties; it emits light after absorbing a photon. 4-(4-Fluorobenzyloxy)Benzaldehyde can also be used to assemble benzyloxyphenyl groups into three dimensional structures by reacting with malononitrile and metal ions.

Acetaldehyde benzyl ethylacetal is a reaction product of acetaldehyde and benzyl alcohol. It is a colorless liquid with a strong, aromatic smell. Acetaldehyde benzyl ethylacetal can be used as an antibacterial agent or as a flavorant for food and beverages. It has shown activity against gram-positive bacteria (including MRSA) and fungi, but not against gram-negative bacteria. The reaction rate is determined by the concentration of the reactants, the pH, and the neutralizing agent.

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Hexahydro-1H-azepine-1-carbaldehyde is a lactam that is formed by the condensation of two amino acids. It is soluble in water and ethanol, but not in ethers. Hexahydro-1H-azepine-1-carbaldehyde melts at temperatures of -30°C to -20°C and has a boiling point of 126°C. The compound is also soluble in chloroform and ethyl acetate, but insoluble in benzene, carbon disulfide, and hexane. Hexahydro-1H-azepine-1-carbaldehyde can be produced by the periodate oxidation of the corresponding dialkyl chloride or sulfoxide or by the reaction of benzylpenicillin with hexamethylphosphoramide.

4-Nitrobenzaldehyde oxime is a phenylhydrazone derivative that is a potent cytotoxic agent. The 1,2-nitration of the benzene ring in 4-nitrobenzaldehyde oxime produces a reactive intermediate that reacts with nucleophilic groups on cellular macromolecules to produce DNA strand breaks and other types of damage. 4-Nitrobenzaldehyde oxime has been shown to have significant anticancer activity against leukemia cells in culture, as well as antibacterial and anticancer activity against Staphylococcus aureus and Escherichia coli.

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3'-(TrifluoroMethyl)[1,1'-biphenyl]-3-carbaldehyde is a coolant and antimicrobial agent. It has been shown to inhibit the growth of bacteria such as Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli in vitro. 3'-(TrifluoroMethyl)[1,1'-biphenyl]-3-carbaldehyde has also been used as a flavoring agent. However, it can be toxic when ingested. The substance is classified as an environmental hazard because of its high toxicity and potential for bioaccumulation.

5-(2-Chlorophenyl)-2-furaldehyde (5Cl-F) is an isomer of 2,5-dihydroxyfuran. The compound has been shown to interact with other molecules in a number of intermolecular reactions. The crystal structure of 5Cl-F was determined using X-ray diffraction and found to be isomorphic with that of the 2,5-dihydroxyfuran. The compound has not been shown to have any interactions with other molecules in the form of a result.

2,4-Hexadienal is a reactive functional group that has been shown to have oxidative DNA damage potential. It is also an asymmetric molecule, which can be synthesized in a multistep process using malonic acid and ethyl decanoate. This molecule has been shown to have reactive nucleophilic properties and is used as a model system for studying the physiological function of 2,4-hexadienal. The activation energy for this compound is around 200 kJ/mol.

1-(3-Chlorophenyl)-3-(3-pyridinyl)-1H-pyrazole-4-carbaldehyde is a resorcinol derivative that is synthesized by the reaction of hydrochloric acid and chalcone. It has been shown to be an inhibitor of the enzyme benzotriazole, which catalyzes the formation of propenone from benzopyran. This research chemical also inhibits the enzyme methanoic, which catalyzes the conversion of propenone to pyrazoline. It has been used as a starting material for heterocyclic derivatives.

Cinnamic aldehyde is an organic compound that is a member of the cinnamyl aldehyde family. It can be found in many plants and is often used as a flavoring agent. Cinnamic aldehyde has been shown to have inhibitory effects on angiosperm phylogeny group and family index, which may help to understand the evolutionary relationships between plant species. This compound also inhibits linear growth in plants, which may be due to its ability to inhibit protein synthesis, cell division, and DNA replication.

Phenanthrene-4-carbaldehyde is a formyl derivative of the polycyclic aromatic hydrocarbon phenanthrene. It is a colourless liquid with an evaporation point at 20°C and a boiling point of 170°C. The compound has been shown to undergo photocyclization and photooxidation when irradiated with ultraviolet light, which are reactions that involve the formation of oxygenated products. Phenanthrene-4-carbaldehyde has also been shown to be oxidised by chloride ions in the presence of oxygen, producing chloride oxide and carbon dioxide. This molecule has been optimised for use in aerosols and mass spectrometry experiments.

5-(3-Trifluoromethyl-Phenyl)-Furan-2-Carbaldehyde is an antioxidant that inhibits the formation of reactive oxygen species. It is synthesized by condensing acetophenone with methylene in the presence of an azide and a propenoic acid. This compound has been shown to have antioxidant activity, as seen in its ability to inhibit the oxidation of malononitrile. 5-(3-Trifluoromethyl-Phenyl)-Furan-2-Carbaldehyde is used as a light stabilizer in plastics and rubbers, and has also been used for the synthesis of pharmaceuticals, including acetaminophen.

Quinoxaline-6-carbaldehyde is a synthetic, cytotoxic compound that inhibits cell growth and induces apoptosis in cancer cells. It has been shown to inhibit the proliferation of G1 phase cancer cells, which may be due to its ability to inhibit protein synthesis and induce DNA fragmentation. Quinoxaline-6-carbaldehyde also has an inhibitory effect on cancer cells with a methoxy group in their a-ring. This compound is more effective when used in combination with pyrazoles. Molecular modeling studies have revealed the binding interactions between quinoxaline-6-carbaldehyde and the active site of human brain tumor cells. The biological properties of this compound have been studied using molecular methods, such as gel electrophoresis and thin layer chromatography.

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Hexadecanal (Palmitaldehyde) is a free fatty aldehyde present in animals.

2-Phenylbutanoic acid (2-Phenylbutyric acid) is used as an industrial intermediate.

2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde is a chemical compound that is an enantiopure chlorinating agent. It is used in the synthesis of medicines and other organic compounds. This chemical compound has been shown to have antimicrobial properties and can be used to create antibiotics such as eperezolid. 2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde is also used in the synthesis of amides and other organic compounds. The reaction system for this compound is very sensitive to acidic conditions and requires a strong acid catalyst for successful completion of the reaction.

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