Aldeídos

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<p>4-(2-Propynyloxy)benzenecarboxaldehyde is an organic chemical compound that is classified as a copper complex. This molecule has been shown to have antibacterial properties against P. aeruginosa and other bacteria. It also possesses a constant antibacterial activity in both acidic and neutral pH conditions, which makes it an efficient method of treatment for bacterial infections. 4-(2-Propynyloxy)benzenecarboxaldehyde has been shown to inhibit the growth of P. aeruginosa by binding to the DNA gyrase enzyme and stopping its function, thus inhibiting bacterial replication. 4-(2-Propynyloxy)benzenecarboxaldehyde also inhibits the synthesis of proteins in neuronal cells, which may be due to its ability to react with carbonyl groups in proteins.</p>

Cinnamaldehyde thiosemicarbazone is a nitrogen-containing molecule that has been shown to have neuroprotective properties. It is also an antioxidant and potent inhibitor of tyrosinase, which is an enzyme involved in the production of melanin. Cinnamaldehyde thiosemicarbazone has been shown to be effective at nanomolar concentrations in the inhibition of tyrosinase. This compound has been shown to be effective in both basic structure and magnetic resonance spectroscopy studies.

<p>Stability Light Sensitive, Temperature Sensitive<br>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<br>References Zilkowski, B., et al.: J. Agr. Food Chem., 56, 4982 (2008)<br></p>

<p>Applications N,N,N-Tributyl-1-butanaminium Salt with (E)-3-Hydroxy-2-propenal is a useful reagent for preparation of crystalline (±)​-​fecapentaene.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Pfaendler, H., et al.: J. Am. Chem. Soc., 108, 1338 (1986);<br></p>

<p>Applications 2,4-Octadienal, predominantly trans,trans &gt;=95%, FG is a useful research chemical for organic synthesis and other chemical processes.<br>References Feng, J., et al.: J. Org. Chem., 82, 1412 (2017); Sun, S., et al.: J. Appl. Phycol., 24, 1003 (2012)<br></p>

<p>Applications 2-Propyl-2-heptenal is an alkene shown as an metabolic by-product of unsaturated fatty acids metabolism to oxylipins.<br>References Montanari, C., et al.: J. App. Microbiol., 115, 1388 (2013);<br></p>

<p>Applications CIS-4-DECENAL (cas# 21662-09-9) is a useful research chemical.<br></p>

<p>Stability Light Sensitive<br>Applications (E,E)-5-[4-(Diethylamino)phenyl]penta-2,4-dienal is used in polymerization process.<br>References Innocenzi, P., et al.: J. Mater Chem., 15, 3821 (2005), Cai, Y., et al.: Polymer, 2006, 47, 6560 (2006),<br></p>

<p>Stability Air Sensitive<br>Applications Oct-7-enal is a useful research chemical, an aliphatic aldehyde isolated from the roots of Cirsium Cipsacolepis.<br>References Takano, S., et al.: Phytochemistry, 26, 435 (1987); Halle, M. B., et al.: RSC Adv., 4, 63342 (2014)<br></p>

<p>2,4-Dihydroxy-6-methylbenzaldehyde is a chemical that is found naturally in a variety of plants. It has been shown to have immunomodulatory and anti-inflammatory effects in vitro and in vivo. 2,4-Dihydroxy-6-methylbenzaldehyde has been shown to reduce the production of inflammatory molecules such as tumor necrosis factor alpha (TNFα) and interleukin 12 (IL-12) by inhibiting the activation of microglia cells. This compound also inhibits LPS induced inflammatory response in human carcinoma cells. 2,4-Dihydroxy-6 methylbenzaldehyde is currently undergoing clinical trials for its potential use in regenerative medicine.</p>

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<p>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.</p>

<p>3-Methyl-p-anizaldehyde is a vanillyl alcohol, which is a natural compound that can be found in vanilla beans. It has been used in the synthesis of vanillic acid and lactams. 3-Methyl-p-anizaldehyde has been shown to react with alkyl halides to form alkylated products. These reactions are catalyzed by an enzyme called alcohol dehydrogenase. This enzyme binds to the hydroxyl group on the 3 position of the vanillin molecule, which is then oxidized to form a functional group called an acetate ester. The reaction occurs at low temperatures and can result in optical activity if it produces a chiral product. 3-Methyl-p-anizaldehyde also reacts with ecteinascidins, which are marine natural products that have potent cytotoxic properties against cancer cells.</p>

<p>Tetrafluoroterephthaldehyde (TFPA) is a reactive aldehyde that can be synthesized in the laboratory by the reaction of trifluoromethanesulfonic acid with an aromatic hydrocarbon or ester compound. TFPA has been used to study the synthesis of supramolecular assemblies and supramolecular chemistry. The radiation-induced formation of TFPA is a useful method for the synthesis of polymers, and the thermal expansion of TFPA is high enough to be used as a thermometer. TFPA has shown chemical stability in both acidic and alkaline media, as well as resistance to radiation and oxidation. TFPA also has a high boiling point, making it useful for desolvation during gas chromatography experiments.</p>

<p>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.</p>

<p>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.</p>

<p>2-Cyanobenzaldehyde is an aldehyde that reacts with nucleophiles such as trifluoromethanesulfonic acid to form a molecule. 2-Cyanobenzaldehyde has potent inhibitory activity against the kinase glycogen synthase kinase 3 (GSK3) and can be used to treat autoimmune diseases. It also reacts with hydrochloric acid in solution to form an intermediate, which is then reacted with glycine and ATP to produce a chiral compound. The product of this reaction has been shown to be active methylene, which was synthesized by asymmetric synthesis.</p>

<p>1-Phenyl-1H-pyrazole-4-carbaldehyde is an antibacterial agent that has been shown to have bactericidal activity against bacteria. It inhibits the growth of bacteria by binding to the pyrazole ring in the bacterial cell wall and blocking the formation of a hydrogen bond. 1-Phenyl-1H-pyrazole-4-carbaldehyde has been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) and Ciprofloxacin resistant Pseudomonas aeruginosa isolates, but not against Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>4-Ethylbenzaldehyde is a chemical compound that belongs to the group of fatty acids. It has been shown to have biological properties, such as antiviral potency and genotoxic effects. This chemical compound also has a gas sensor property and is used as an exothermic reactant in organic synthesis reactions. 4-Ethylbenzaldehyde has been shown to inhibit the growth of bacteria, fungi, and viruses by blocking the synthesis of viral nucleic acid or inhibiting viral protein synthesis. The magnetic resonance spectroscopy (NMR) spectral data for 4-ethylbenzaldehyde show that this chemical compound contains two methyl groups, one on each side of the benzene ring, with a hydroxyl group on one end. The carbon atoms are bonded together in an alternating pattern of single and double bonds. The molecular formula for 4-ethylbenzaldehyde is C9H10O2.</p>

<p>2-(1H-Pyrazol-1-yl)benzaldehyde is a synthetic chemical compound that is used in the preparation of coupling reactions. It has been shown to be an efficient reagent for the synthesis of 2-bromobenzaldehyde and pyrazole. The molecule has a hydrazone attack, which can be coupled with 2-bromobenzaldehyde, with or without the use of an additional base such as sodium methoxide. This reaction can be carried out at room temperature and does not require any harsh conditions. 2-(1H-Pyrazol-1-yl)benzaldehyde also belongs to the family of aldehydes, which are molecules containing a carbon group that is connected to two hydrogen groups (i.e., RCH=O). Hydrogenation of this type of molecule gives rise to alcohols (RCHOH).</p>

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<p>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</p>

3,4-Dichlorobenzaldehyde is a monosubstituted aromatic organic compound with inhibitory effects. 3,4-Dichlorobenzaldehyde has shown significant antifungal activity against Candida albicans and Saccharomyces cerevisiae. It also inhibits the growth of certain cancer cells in cell culture studies. 3,4-Dichlorobenzaldehyde has been found to have anti-inflammatory properties and would be effective in treating inflammatory diseases such as asthma or arthritis. This compound has been shown to have significant effects on energy metabolism and fatty acid synthesis by inhibiting enzymes that are involved in these processes. 3,4-Dichlorobenzaldehyde can also be used to treat metabolic disorders such as diabetes mellitus type II and hyperlipidemia by inhibiting enzymes that are involved in these processes.

<p>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.</p>

Butyraldehyde is a colorless to yellowish liquid with a strong, pungent odor. It is soluble in water and has an acidic pH of 2.6-3.0. Butyraldehyde is used as a chemical intermediate for the production of polyvinyl acetate and can be made by reacting acetic acid with butanol or butyl acetate. This chemical reacts with human serum albumin at low concentrations and may have biological properties such as catalyzing the conversion of picolinic acid to nicotinic acid, which aids in the prevention against infectious diseases. Butyraldehyde also has synergistic effects when used with picolinic acid, increasing its effectiveness in combating infection.

<p>Pyridine-3-carboxaldehyde is a heterocyclic compound that is structurally related to nicotinic acid and picolinic acid. It has been shown to have anti-tumor activity, with hl-60 cells as the model system. Pyridine-3-carboxaldehyde has also been shown to be toxic to bacteria in biological studies. The chemical stability of this compound was studied by Langmuir adsorption isotherm and electrochemical impedance spectroscopy. It was found that pyridine-3-carboxaldehyde is stable at a pH range of 7 to 8 and at temperatures up to 60 degrees Celsius.</p>

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<p>Valiphenal is a chemical compound that belongs to the amide class. It has been shown to control the growth of various bacterial strains, such as Escherichia coli and Salmonella enterica serovar Typhimurium. Valiphenal inhibits lipid biosynthesis in bacteria by binding to bacterial matrix effect enzymes, which are involved in fatty acid synthesis. This inhibition leads to a decrease in the production of lipids, which are an important component of bacterial cell membranes. Valiphenal also inhibits mitochondrial cytochrome c oxidase and can be used as an analytical tool for determining the presence of this enzyme in cells. Valiphenal is also used as an agrochemical to control pests on vegetables such as aubergines. Valiphenal is extensively metabolized by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</p>

<p>6-(Hydroxymethyl)pyridine-2-carboxaldehyde is a ligand that has anisotropic magnetic properties. It crystallizes in an orthorhombic system, and its structure consists of two iron atoms (II) coordinated by two hydrazone groups and one carboxylate group. The compound is dimeric, with each unit consisting of two iron atoms (II) coordinated by two hydrazone groups and one carboxylate group. The compound exhibits ferromagnetic properties, being paramagnetic at room temperature. In crystallography studies, it was found that the 6-(hydroxymethyl)pyridine-2-carboxaldehyde adducts are tetranuclear with a helicate geometry around the Fe(II) atom. This compound is also paramagnetic at room temperature due to the presence of unpaired electrons on the two Fe(II) centers.</p>

1-Allyl-1H-benzimidazole-2-carbaldehyde is a dipolar compound that can be synthesized from the reaction of 1,3-diphenylazomethine and allyl bromide. It is an orange solid that has been shown to form cycloadducts with alkenes. The selectivity of this reaction depends on the substituents on both reactants, with electron withdrawing groups increasing the rate of substitution. Dipolar cycloaddition theory predicts that 1-allyl-1H-benzimidazole-2-carbaldehyde undergoes intramolecular cycloaddition to form a six membered ring in which one carbon atom is shared between two adjacent atoms.

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<p>N-Methyl-N-hydroxyethyl-4-aminobenzaldehyde (NHABA) is a bathochromic molecule that absorbs light at wavelengths of 400 to 500 nm. It is reactive and reacts with metal cations to form chromophores. NHABA has been shown to be a fluorescent probe for the detection of tyrosinase and autophagy in human serum. It also has inhibitory properties against tyrosinase, which may be due to its ability to inhibit the formation of melanin. NHABA is used as an analytical chemistry reagent for the determination of ammonia, nitrite, and nitrate ions in water samples. This molecule can also be used as a chemosensor for the detection of phenolic compounds in water samples.</p>

<p>4-Nitro lenalidomide is an organic compound that is a derivative of the drug lenalidomide. It is synthesized by reacting 2-nitrobenzaldehyde with amines, yielding 4-nitro-N-(2-chloroethyl)-N-(2,3-dihydroxypropyl)benzamide or 4-nitrolenalidomide. This reaction occurs in tetrahydrofuran (THF) as a solvent and in the presence of sodium borohydride (NaBH4). The four nitro groups are used to control the enantiomeric purity of the product. The chemical formula for 4-nitro lenalidomide is C12H14ClNO2.</p>

2-Fluoro-5-hydroxybenzaldehyde (2FHBA) is an olefinic compound that is synthesized from 2,5-dihydroxybenzaldehyde by reductive amination with formaldehyde. The configuration of 2FHBA is dependent on the dihedral angle between the two olefinic groups. Liquid chromatography has been used to analyze the metabolic pathway of 2FHBA in rats and humans. This study showed that tyramine and aligned are metabolites of 2FHBA in rats, while crystallized and emission are metabolites in humans. The positron emission studies also showed that 2FHBA was metabolized by erythrocytes in vitro to produce positron emission.

<p>2-Phenoxyacetaldehyde is a reactive molecule that has been shown to inhibit the growth of hematopoietic cells. It also inhibits the production of active enzymes, such as amylase, by interfering with the nucleophilic attack and oxidation of 2-phenoxyacetaldehyde. The synthesis methods for 2-phenoxyacetaldehyde include homogeneous catalysts and chemical reactions. This molecule has been used in detergent compositions, but it is not suitable for use in food contact materials because of its toxicity.</p>

<p>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.</p>

5-hydroxymethylfurfural (5-hmf) is an organic compound that is produced when a carbohydrate or sugar undergoes oxidation. It is used as an additive in animal feed and as an industrial chemical. 5-hmf is a solid catalyst that can be used at high temperatures, making it suitable for use in the production of 2,6-dihydroxybenzoic acid. The reaction mechanism of 5-hmf involves the dehydration of furfural to form 5-hydroxymethylfurfural. This process occurs when a molecule of water reacts with furfural to produce two molecules of 5-hmf. The reaction may be accelerated by introducing heat, which breaks down the hydrogen bonds between the molecules of furfural and water.

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<p>(R)-Perillaldehyde is an activated cardenolide that binds to flavoproteins and inhibits the oxygenation of 4-hydroxycoumarin. It is a stereoselective, substrate binding, and oxygenated flavoenzyme inhibitor. The orientation of perillaldehyde with respect to the flavin may be important for its activity in the enzyme's active site.</p>

<p>4-tert-Butylbenzaldehyde is an organic compound with the molecular formula CH3COCH2C6H5. It is a viscous liquid that is insoluble in water and has a boiling point of 146 °C. 4-tert-Butylbenzaldehyde reacts with cationic surfactants to form polymeric micelles, which are spherical structures composed of many small spherical subunits. These polymeric micelles are used as model systems for studying the properties of surfactant aggregates in solution. The reaction mechanism for this polymerization process involves the oxidation of 4-tert-butylbenzaldehyde by hydrogen peroxide and the subsequent condensation of 4-tert-butylbenzoic acid with malonic acid or other cinnamic acid derivatives to form the corresponding esters. The oxidized product, 4-tert-butylbenzoic acid, can be regenerated by boiling a mixture containing it</p>

<p>Ferrocenecarboxaldehyde is a fatty acid with a ferrocene carboxylic acid group. It has been shown to have antimicrobial activity against bacteria, fungi, and yeast when it was mixed with nitric acid. Ferrocenecarboxaldehyde can be synthesized by reacting ferrocene with glycerol in the presence of sulfuric acid. The reaction mechanism of this synthesis is as follows: The structural analysis of ferrocenecarboxaldehyde has been studied using FT-IR spectroscopy and NMR spectroscopy. The chemical structure of ferrocenecarboxaldehyde is as follows: The asymmetric synthesis of ferrocenecarboxaldehyde is shown below:</p>

<p>Furfural is a five-carbon aldehyde produced by the hydrolysis of pentoses. It has been used as an industrial solvent, plasticizer, and fuel. Furfural is also used to produce butanol and biofuels. Furfural can be oxidized in the redox cycle to produce active oxygen species that are reactive with other biological molecules. Furfural is also used as an inhibitor of acetaldehyde formation in beer production. This molecule has two forms: the cis form (C3H4O) and the trans form (C3H3O). The cis form has a chemical structure of CH2=CH-CH2OH, whereas the trans form is CH=CH-CH2OH.</p>

1-Methyl-2-imidazolecarboxaldehyde is a compound that has been studied for its redox potential, which is the measure of the tendency of a molecule to gain or lose electrons. 1-Methyl-2-imidazolecarboxaldehyde has shown to be an excellent candidate as an electrochemical probe. The molecule has also been shown to bind chloride ions in water, forming a tetradentate chelate ring. This type of chelate ring is formed between two nitrogen atoms and four oxygen atoms from the water molecule. The compound forms hydrogen bonds with other molecules in its vicinity, including hepg2 cells and chloride ions.