Aldéhydes

Stability Light Sensitive, Temperature Sensitive
Applications (2E,4E,6E)-2,4,6-Nonatrienal is an unsaturated aldehyde that is a natural volatile constituent of aggregation pheromones produced by male flea beetles. (2E,4E,6E)-2,4,6-Nonatrienal is also found in licorice root, one of the widely used herbs for its
References Zilkowski, B., et al.: J. Agr. Food Chem., 56, 4982 (2008)

2-Hydroxy-4-(trifluoromethyl)benzaldehyde is an analgesic and anti-inflammatory agent that belongs to the pyrazole family. It has shown analgesic and anti-inflammatory effects in animal studies. 2-Hydroxy-4-(trifluoromethyl)benzaldehyde has been shown to be a potent inhibitor of cyclooxygenase (COX), which is responsible for prostaglandin synthesis, and as such, may have potential as a treatment for inflammatory conditions such as rheumatoid arthritis. This drug also inhibits the production of nitric oxide, which is involved in vasodilation and increased blood flow. 2-Hydroxy-4-(trifluoromethyl)benzaldehyde has been demonstrated to inhibit COX enzymes by forming a covalent bond with active site serine residues on the enzyme. The docked complex shows hydrogen bonding interactions between the hydroxyl group of 2

4-Cinnolinecarboxaldehyde is an organic compound that belongs to the group of cinnoline. It is a colorless liquid that can be used as a precursor in the production of aluminum metal. 4-Cinnolinecarboxaldehyde reacts with lithium aluminum hydride to form a compound that can be used as a reducing agent in organic chemistry. 4-Cinnolinecarboxaldehyde is also used as a precursor for preparing other compounds, such as lithium aluminum hydride and lithium aluminum trihydride.

Benalaxyl is an insecticide that belongs to the group of organochlorine compounds. It is a chiral compound that has been used in analytical methods for wastewater treatment and as an anti-fouling agent. Benalaxyl has been shown to possess acute toxicity, based on the results of redox cycle experiments, cell nuclei studies, enzyme activities, and rat liver microsomes. Toxicological studies have also shown that benalaxyl can cause high levels of resistance in nutrient solutions, energy metabolism, and synthesis methods.

4-Bromofuran-2-carbaldehyde is a synthetic compound that has been shown to have antioxidant properties. It contains an electron-donating carbonyl group and an electron-withdrawing bromine atom. 4-Bromofuran-2-carbaldehyde is useful in the treatment of endophytic fungi infections, as it inhibits the synthesis of ergosterol, which is an important component of the fungal cell membrane. The molecule's conformational properties are also important for its biological activity, as they enable it to act as a chiral ligand by binding to proteins in a way that will inhibit their function. In addition, 4-bromofuran-2-carbaldehyde has been shown to be effective against cancer cells in vitro, particularly against MMCF7 cells. This may be due to its ability to bind to DNA and prevent transcription or replication of DNA strands.

3,5-Dichloro-4-pyridinecarboxaldehyde is a synthetic heterocycle that has been studied for its pharmacokinetic properties. The compound has the ability to bind to the active site of metalloporphyrin and inhibit the enzyme's activity. This inhibition leads to an increase in the levels of homologous aldehydes, which are oxidized by hydrogen peroxide to produce electrosprays. 3,5-Dichloro-4-pyridinecarboxaldehyde also has a number of oxidation products that have been found in experiments using purines as substrates.

Succinicsemialdehyde is a semialdehyde that is formed by the oxidative degradation of succinic acid. Succinicsemialdehyde has been shown to have high affinity for 5-HT3 receptors, which are found in the gastrointestinal tract and are involved in intestinal motility and bowel disease. The 5-HT3 receptor has been shown to be an important target for the treatment of irritable bowel syndrome. This semialdehyde also inhibits polymerase chain reaction (PCR) activity, which may be due to its ability to inhibit DNA synthesis. Succinicsemialdehyde has been shown to inhibit enzymes involved in energy metabolism, such as glutamate dehydrogenase and pyruvate formate lyase. The structural analysis of this molecule shows a keto group at C2, which indicates that it is a keto acid.

p-Anisaldehyde dimethyl acetal is a broad-spectrum antimicrobial that can be synthesized from anisaldehyde and dimethoxyacetal. It has been shown to have anticancer properties in vitro. p-Anisaldehyde dimethyl acetal has also been shown to inhibit the growth of HL60 cells, which are specialized white blood cells. This compound was found to increase neuronal death and induce cachexia in mice. The molecular weight of p-Anisaldehyde dimethyl acetal is 244.24 g/mol, with a melting point of -14 °C and a boiling point of 156 °C. The molecule contains one asymmetric center, one hydrogen bond, one non-bonding electron pair, and no double bonds. This compound has acidic properties and it reacts with vitamin D3 in a cationic polymerization process at alkaline pH levels.

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10-Chloro-9-anthraldehyde is an antibacterial agent that exhibits activity against a wide variety of bacteria. It is the product of the photomodification of anthracene, which is activated by ultraviolet light to produce 10-chloro-9-anthraldehyde. The preliminary functional studies of this compound indicate that it may be used in coatings for polymers and textiles as well as in innovative applications such as fluorescence labeling and immunoassays. 10-Chloro-9-anthraldehyde also has a protonation site at the 9 position, making it useful for conjugation with biomolecules.

5-Bromo-2-furaldehyde is a chemical compound that belongs to the class of heterocycles. It is used in industry as a precursor for the synthesis of other organic compounds. 5-Bromo-2-furaldehyde has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. The use of this chemical has been linked with autoimmune diseases and cancer development in animal models. 5-Bromo-2-furaldehyde is an environmental pollutant that can enter the body by ingestion or inhalation, and it can cause irritation of the skin, eyes, nose, throat, and lungs. This chemical is also known as amide or suzuki coupling reaction (SCR).

2-Methylbut-2-enal is an aldehyde that belongs to the class of fatty acid. It has been shown that 2-methylbut-2-enal inhibits the growth of bacteria by binding to the anhydrous sodium and tiglic acid in the bacterial cell wall. This binding prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division. 2-Methylbut-2-enal also inhibits locomotor activity in mice, which may be due to its ability to inhibit acetylcholinesterase.

2-Fluoro-4-hydroxybenzaldehyde is an oxidative compound that is a model compound of phenolic compounds. It can be used to synthesize 2,6-dichloroquinone and 2,5,7,8-tetrachlorodibenzo[p]fluoranthene. The metabolic pathway for this compound starts with the oxidative decarboxylation of L-tyrosine to form 4-hydroxyphenylpyruvic acid. This compound is then oxidized by cytochrome P450 enzymes to form 4-(2'-oxo)phenol. The 4-(2'-oxo)phenol can be methylated by S-adenosylmethionine in order to form 2-fluoro-4-hydroxybenzaldehyde.

5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%.

3-Chloro-1H-indole-2-carbaldehyde is a bifunctional reagent that can be used to form amides. It reacts with primary and secondary amines, as well as dialkyl and methylene amines, to produce the corresponding chloro-, phenylhydrazine-, or nitrosoaminoureas. This reaction is intramolecular and yields the desired product in high yield. The reactant can also be used as a chloride source. 3-Chloro-1H-indole-2-carbaldehyde is manufactured by reacting phenylhydrazine with chloroacetic acid in an organic solvent at room temperature (25°C).

Adrenalone is a caffeic acid derivative that contains a hydroxyl group. It is used in the treatment of infectious diseases, bowel disease, and autoimmune diseases. Adrenalone inhibits bacterial growth by interfering with cell wall synthesis, which prevents the formation of new cell walls and leads to bacterial death. It also inhibits the production of dopamine by acting on an amine oxidase enzyme. This drug has been shown to be effective in treating inflammatory bowel disease (IBD) in both mice and humans due to its ability to inhibit pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-6.

4-Bromo-2-hydroxybenzaldehyde is a versatile building block that can be used as a reaction component to synthesize other compounds. 4-Bromo-2-hydroxybenzaldehyde is a useful intermediate in the manufacture of pharmaceuticals, pesticides, and herbicides. This chemical also has various applications in research and industry. It is an important reagent for the production of polymers and resins, as well as being an essential raw material for the synthesis of pharmaceuticals and agrochemicals.

5-Nitrothiophene-2-carboxaldehyde (5NT) is a chemical compound that belongs to the class of dihedral molecules. It is commonly used as an antimicrobial agent and has been shown to have amoebicidal activity in tissue culture. 5NT also inhibits cell growth and proliferation in certain bacteria, such as Staphylococcus aureus strains, by interfering with DNA replication and protein synthesis. Although 5NT is not active against other types of bacteria, it has been shown to be effective against MRSA in laboratory studies. The biological properties of 5NT are still being studied.

Heptaldehyde is a colorless liquid with a pleasant, sweet odor. It is used in the production of polyvinyl chloride and other chemicals. In addition, it can be an important biomarker in environmental studies. Heptaldehyde is produced by the reaction of ethyl decanoate with water vapor or methyl ethyl ketone. It is also an inhibitor of acetylcholinesterase, which may be due to its hydroxyl group and acetyl group. Furthermore, heptaldehyde has been shown to react with p-nitrophenyl phosphate to form p-nitrophenol. The following table outlines the chemical properties of heptaldehyde: Molecular formula: C7H8O Molecular weight: 112.14 g/mol Boiling point (°C): 212 °C Melting point (°C): -78 °C Density (g/cm3): 1.096

Paraformaldehyde is a carcinogenic substance that belongs to the family of heterocyclic compounds. It reacts with water vapor in the air to form formaldehyde, which is responsible for its fluorescence properties. Paraformaldehyde has been used as a probe for DNA and RNA and can be used as an indicator for nonsteroidal anti-inflammatory drugs. The reaction mechanism of paraformaldehyde is not well understood and it has been shown that it reacts with p-hydroxybenzoic acid, polymerase chain, and water vapor. This compound can be found in soybean extract or fetal bovine serum. Paraformaldehyde is usually detected using a plate test or analytical methods such as high performance liquid chromatography (HPLC).

Terephthalaldehyde chloride is a water-insoluble, white solid that is soluble in organic solvents. It forms a protective layer on metal surfaces and plastics, preventing corrosion and microbial growth. Terephthalaldehyde chloride has been shown to be effective against Escherichia coli, Klebsiella pneumoniae, Bacillus subtilis, Pseudomonas aeruginosa, Staphylococcus aureus, and Salmonella enterica. Terephthalaldehyde chloride's antimicrobial activity is attributed to its acid complex with phosphorus pentoxide and electrochemical impedance spectroscopy data indicate that it reacts with the anionic sites of bacterial cell walls. Terephthalaldehyde chloride does not react with human serum proteins or ester linkages; however, it has toxic effects on mice at high doses.

3,5-Bis(trifluoromethyl)benzaldehyde is a synthetic compound that has been shown to inhibit cancer cell growth. It is a chromatographic reagent and an intermediate in the production of pharmaceuticals. 3,5-Bis(trifluoromethyl)benzaldehyde was shown to bind to the amino group of proteins and inhibit the synthesis of protein inhibitors. This compound also binds to cholesterol esters and causes lipid peroxidation, leading to cell death in cancer cells.

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2-Hydroxy-4-fluorobenzaldehyde is a chemical used as a diagnosis agent to detect radiation exposure. It reacts with magnesium and water molecules to form an amination reaction that produces hydrogen fluoride gas. 2-Hydoxy-4-fluorobenzaldehyde has been shown to have the ability to penetrate into mitochondria, which may be related to its use in the treatment of hepatitis. The chemical structure of this compound is similar to salicylaldehyde, which is used as a reagent for formylation reactions and optical properties. It has also been shown that 2-hydroxy-4-fluorobenzaldehyde can act as a fluorescence probe for the detection of hydrophobic regions on proteins.

4-Acetoxybenzaldehyde is a compound with an acetyl group attached to the benzene ring. It is potentially toxic to cells and has been shown to produce reactive oxygen species (ROS) in v79 cells, which can lead to cell death. The biological properties of 4-acetoxybenzaldehyde are not well understood, but it has been shown to have antioxidant properties in other studies. This compound also reacts with amines, forming acetamides and amides. 4-Acetoxybenzaldehyde is found in environmental pollution as a result of its presence in the atmosphere and its use as a solvent. It was first synthesized by the reaction of coumaric acid and acetyl chloride with formaldehyde at reflux temperature. The compound can be purified by chromatographic methods or mass spectrometric analysis.

1H-Indole-2-carbaldehyde is a solvent that has been used in the protein data and molecular modeling study. The 1H NMR spectrum of this compound showed an intense signal at δ 4.8 ppm, corresponding to the hydroxyl proton. This solvent also has fluorescence properties, as shown by its photophysical and structural analysis. The 1H-indole-2-carbaldehyde molecule has an active methylene group and an oxindole ring with amine substituents.

4-Fluorobenzaldehyde oxime is a phenylhydrazine derivative that reacts with an aromatic amine to form a ternary complex. The reaction time for this process is short, and the yield of the product is high. 4-Fluorobenzaldehyde oxime also reacts with an aromatic amine to form an ion-pair. It can react with acidic hydrogen donors such as peracids and it also has high hydrogen bonding interactions. 4-Fluorobenzaldehyde oxime is used in pharmacological agents as well as other chemical reactions, including halogenation.

1H-Pyrazole-4-carbaldehyde is a chemical compound that inhibits the growth of bacteria by binding to the enzyme ribonucleotide reductase. It has been shown to have significant antifungal activity against Candida albicans and Saccharomyces cerevisiae, as well as in vitro antifungal activity against other fungi. The 1H-pyrazole-4-carbaldehyde has also been found to inhibit xanthine oxidase and nitric oxide synthase (NOS) in vitro and in vivo, which may be due to its ability to reduce oxidative stress. This chemical compound is a coumarin derivative and contains a pyrazole ring.