Aldehídos

<p>Please enquire for more information about 2-(3-Trifluoromethylphenoxy)-5-nitrobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-(4-Trifluoromethylphenoxy)-5-nitrobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-(5-(Trifluoromethyl)-2-pyridyl)piperazinecarbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>4-Piperazin-1-yl-benzaldehyde (PPBA) is a natural product that has been shown to have effects on animals and cells. PPBA can be used as an antidote for sulfite poisoning, which is caused by the ingestion of sulfites in food or drink. The mechanism of PPBA's effects is not fully known, but it may involve the inhibition of sulfite reductase, which converts sulfites into sulfates. It also reversibly forms a complex with the transition state of the reaction, enhancing the rate of this reaction. This enhancement is due to a low detection limit and shift in solution temperature. PPBA has been shown to have fluorescence and fluorescent properties when exposed to light, making it useful for endogenous labeling.</p>

Please enquire for more information about N-[3-(1,1,2,2-Tetrafluoroethoxy)phenyl]formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-((4-methylphenyl)carbonyl)piperazinecarbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Zolpidem is a sedative-hypnotic drug, which belongs to the class of imidazopyridines. It has a strong affinity for GABA receptors, and can be used as a treatment for insomnia. Zolpidem's chemical structure is similar to that of benzodiazepines. Zolpidem is an acidic compound with a pKa of 3.6. It has been shown to elute from HPLC columns at a hydrodynamic flow rate of 0.5 mL/min on the column of LiChrosorb RP-18e (250 × 4 mm). The optimum pH for chromatographic separation was found to be 4-5. Multiresponse analysis showed statistically significant differences between different batches of zolpidem in terms of particle size, shape and size distribution, surface area and surface charge. Zolpidem carbaldehyde is an organic compound that is used as an intermediate in the production of drugs such as zol</p>

<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>

<p>Please enquire for more information about 4-((4-bromo-2-methyl-5-oxo-1-phenyl(3-pyrazolin-3-yl))methoxy)-3-methoxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Nitro-2-(2'-pyridinethio)benzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</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-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>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>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>Applications CIS-4-DECENAL (cas# 21662-09-9) is a useful research chemical.<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>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>

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.

<p>1-Naphthalenylsulfonyl-Ile-Trp-aldehyde is a recombinant protein that has protease activity. It is a serine protease that cleaves proteins at the amino acid sequence Ser-Xaa-Gly or Ser-Xaa. The recombinant protein has been shown to have proteolytic activity and can be used in assays to measure the amount of β-catenin, collagen, and growth factor in cells. 1-Naphthalenylsulfonyl-Ile-Trp-aldehyde also binds to monoclonal antibodies and can be used as a neutralizing agent for these proteins. This recombinant protein also has been shown to inhibit the growth of lung fibroblasts.</p>

<p>Please enquire for more information about 2-Methyl-6-(trifluoromethyl)nicotinaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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.</p>

<p>Please enquire for more information about 5,6,7,8-Tetrahydronaphthalene-1-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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>

<p>2-Furaldehyde diethylacetal is a synthetic compound that has been used in the synthesis of calcium carbonate. It is also a potent inhibitor of p. aeruginosa and other bacteria, as well as organic acids and halogen compounds. It reacts with hydroxy groups to form aldehydes, which are then oxidized to form carboxylic acid derivatives. The reaction mechanism for this compound is not well understood, but it is thought that the activation energy for the reaction may be low due to the presence of a furfural functional group.</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>Please enquire for more information about 4(5)-Methyl-1H-imidazole-2-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

<p>Please enquire for more information about 2-Cyanopyridine-4-carboxaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(Methylthio)propionaldehyde (MTPA) is a hydroxy methyl fatty acid that is used as an intermediate in the synthesis of ethyl decanoate. MTPA has been shown to be toxic at high doses, with death occurring in rats after a single oral dose of 30 mg/kg. The toxicity of MTPA may be due to its reactive nature and ability to form acrolein and malondialdehyde, which are known to have cytotoxic effects on cells. 3-(Methylthio)propionaldehyde can also inhibit microbial metabolism by inhibiting microbial growth and decreasing microbial activity. This inhibition is mediated by the inhibition of enzymes such as fatty acid synthase and acetyl-CoA carboxylase. 3-(Methylthio)propionaldehyde also inhibits the production of ATP in bacteria, leading to cell death.</p>

<p>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.</p>

<p>Please enquire for more information about Dexamethasone-δ17,20 21-aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</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.

Please enquire for more information about Succinaldehyde bis(dimethyl acetal) including the price, delivery time and more detailed product information at the technical inquiry form on this page

<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>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>

<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>

<p>3-(Chloromethyl)-4-methoxybenzaldehyde is a natural product that can be extracted from the rhizomes of the plant. It has been shown to have antibacterial activity in laboratory experiments and has been used in traditional medicine for the treatment of fungus infections. 3-(Chloromethyl)-4-methoxybenzaldehyde is an imidazolylmethyl derivative with a hexane structure. It reacts with hydrochloric acid to form a molecule called chloromethylation, which is also known as an esterification reaction. Piperazine acts as a catalyst in this reaction, increasing its scalability and making it suitable for large-scale production. The compound exhibits radical scavenging activity, which may be due to its ability to donate electrons or hydrogen atoms to free radicals.</p>

<p>2-Hydroxy-1-naphthaldehyde is a redox potential chemical that has been shown to have anticancer activity in vitro and in vivo. It inhibits the growth of cells by binding to iron, which is important for many biological processes including DNA synthesis. 2-Hydroxy-1-naphthaldehyde has also been shown to have metal carbonyl reactivity and fluorescence properties that may be useful as a fluorescent probe. 2-Hydroxy-1-naphthaldehyde binds to iron ions through hydrogen bonding interactions, forming an octahedral complex with six ligands. The compound also has coordination geometry that can be described as either trigonal bipyramidal or square planar, depending on the solvent used. This data was obtained by x-ray diffraction studies of crystalline solids. The compound's Langmuir adsorption isotherm was found to be linear at low concentrations and shifted to nonlinear behavior at higher concentrations. The</p>

<p>Trifluoroacetaldehyde methyl hemiacetal is a chemical compound that inhibits protein synthesis by binding to the ribosomal RNA in microsomes isolated from rat liver. Trifluoroacetaldehyde methyl hemiacetal has been shown to be a bifunctional inhibitor of progesterone receptor, which is an important component of the cell membrane and has been implicated in cancer and bone resorption. Trifluoroacetaldehyde methyl hemiacetal is also effective at inhibiting desflurane-induced anesthesia in rats.</p>

<p>Please enquire for more information about 1-Benzyl-5-ethoxy-1H-indole-3-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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).</p>

<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>

<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.</p>

<p>Please enquire for more information about 4-Bromobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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%.</p>

<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>Trans-2-nonenal is a monoclonal antibody that recognizes the physiological function of cardiac and rat liver microsomes. It has been shown to inhibit enzyme activities in both cell lines. Trans-2-nonenal has also been shown to protect against ischemia/reperfusion injury in rats by reducing the release of intracellular Ca2+ and ATP levels. Trans-2-nonenal is genotoxic and induces oxidative injury, which may be due to its ability to react with caproic acid to form reactive oxygen species.</p>

<p>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.</p>

2-Chloromalonaldehyde is a reactive chemical that can be used as a pharmaceutical intermediate. It has been shown to have anti-inflammatory properties and is often used in pharmaceutical preparations. 2-Chloromalonaldehyde has shown an ability to bind with integrin receptors and inhibit the production of pro-inflammatory molecules, such as prostaglandins. This compound has also been shown to have a photoelectron spectrum that includes an intramolecular hydrogen bond, which contributes to its biological activity.

<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>

<p>2-Hydroxy-3-(trifluoromethoxy)benzaldehyde is a coordination compound that is used as a ligand. It has two-dimensional and crystal structures. The ligated molecule is usually coordinated to the metal ion, forming a dimer.</p>