Aldéhydes
Les aldéhydes sont des composés organiques contenant un groupe carbonyle (C=O) lié à au moins un atome d'hydrogène. Ces composés polyvalents sont fondamentaux dans diverses réactions chimiques, notamment l'oxydation, la réduction et l'addition nucléophile. Les aldéhydes sont des building blocks essentiels dans la synthèse de produits pharmaceutiques, de parfums et de polymères. Chez CymitQuimica, nous proposons une large sélection d'aldéhydes de haute qualité pour soutenir vos applications de recherche et industrielles.
8576 produits trouvés pour "Aldéhydes"
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(E)-2-Octenal
CAS :(E)-2-Octenal is a reactive compound that is produced by the degradation of unsaturated fatty acids. It has been shown to have antioxidant properties, which may be due to its ability to inhibit the activity of lipoxygenase and cyclooxygenase enzymes. (E)-2-Octenal also inhibits bacterial growth through genotoxic effects, such as DNA damage and mutations. The chemical ionization mass spectrometry method has been used for identification and quantification of (E)-2-octenal in a variety of natural products, including ethyl decanoate, caproic acid, and galacturonic acid.
Formule :C8H14ODegré de pureté :Min. 95 Area-%Couleur et forme :Clear LiquidMasse moléculaire :126.2 g/mol6-Methoxy-2-naphthaldehyde
CAS :6-Methoxy-2-naphthaldehyde is a nonsteroidal antiinflammatory drug that belongs to the class of naphthalenes. It inhibits the formation of inflammatory prostaglandins, which are mediators of pain and inflammation. 6-Methoxy-2-naphthaldehyde has been shown to have cytotoxic effects on cancer cells and in vitro studies have shown that it can induce cell lysis. It has also been shown to be a potent fluorescence probe for use in biological applications. This compound binds to human serum proteins by hydrogen bonding interactions, which may affect its pharmacokinetic properties. In addition, this compound has been shown to inhibit the activity of detoxification enzymes such as CYP 2C9 and 2D6 at high concentrations, which may lead to unwanted side effects such as nausea or vomiting. The molecular docking analysis of 6-Methoxy-2-naphthaldehyde with the active site of human liver alcohol dehydrogenFormule :C12H10O2Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :186.21 g/mol2,4-Dimethoxy-5-methylbenzaldehyde
CAS :2,4-Dimethoxy-5-methylbenzaldehyde is an aryl aldehyde that can be synthesized from 2,4-dimethoxyphenol and methyl benzoate. It can also be produced by condensation of benzaldehyde with chloroform in the presence of zinc chloride. This compound is used in the production of various pharmaceuticals, including antihistamines, antidepressants, and antipsychotics.Formule :C10H12O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :180.2 g/mol5-Benzyloxyindole-3-carboxaldehyde
CAS :5-Benzyloxyindole-3-carboxaldehyde is a merocyanine dye that can be used as an antimycobacterial agent in cell culture. It is also fluorescent and has been shown to inhibit the growth of Mycobacterium tuberculosis. 5-Benzyloxyindole-3-carboxaldehyde has been synthesised by reacting 5,5′-dibenzoyloxydihydropyrene with indole and benzaldehyde. The hydrolysis of this compound yields the corresponding carboxylic acid and benzoic acid, which are then converted to the desired product by action of sodium ethoxide. Merocyanine dyes are characterized by a distinctive absorption band in the visible region at about 540 nm. These compounds have also been shown to inhibit renal cells, which may be due to their ability to act as nucleophiles or tautomers.
Formule :C16H13NO2Degré de pureté :Min. 95%Couleur et forme :Off-White PowderMasse moléculaire :251.28 g/mol3-Carboxybenzaldehyde
CAS :3-Carboxybenzaldehyde is a hydroxy aromatic compound with a molecular formula of C8H6O2. It is a synthetic chemical that can be used as an intermediate in the synthesis of other compounds, such as polycarboxylic acids. 3-Carboxybenzaldehyde has been shown to be an effective substrate for binding to polycarboxylic acid enzymes and activating them. This reaction generates the corresponding carboxylate product and releases CO2. 3-Carboxybenzaldehyde has also been used as a reactant in asymmetric synthesis reactions and shown to have some structural similarities with benzene ring structures.Formule :C8H6O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :150.13 g/mol2,4-Dimethoxy-6-methylbenzaldehyde
CAS :2,4-Dimethoxy-6-methylbenzaldehyde is a biomolecular that belongs to the class of depsidones. It is a tetracyclic compound that has been isolated from the fungus Antrodia camphorata and the lichen Xanthoria polycarpa. 2,4-Dimethoxy-6-methylbenzaldehyde has been shown to inhibit the growth of fungi by preventing oxidative phosphorylation in mitochondria. This compound also shows regioselectivity for phenanthrenes, which are aromatic hydrocarbons with two benzene rings and one or more methyl groups on each ring. The synthesis of 2,4-dimethoxy-6-methylbenzaldehyde is achieved through a Witting reaction between olefinic compounds and diethyl malonate in the presence of base. 2,4-Dimethoxy-6-methylbenzaldehyde can also be synthesized by oxidizing dibFormule :C10H12O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :180.2 g/mol2,4-Dichloro-6-hydroxybenzaldehyde
CAS :2,4-Dichloro-6-hydroxybenzaldehyde is a potential antineoplastic agent that inhibits mitochondrial function and induces apoptosis. This drug blocks the mitochondrial membrane potential and inhibits ATP production by blocking the mitochondrial respiratory chain complexes I and III. 2,4-Dichloro-6-hydroxybenzaldehyde has been shown to inhibit tumor cell growth in culture and in animal models of cancer. It also selectively kills tumor cells with low levels of cisplatin resistance through concurrent inhibition of mitochondria and caspase activation. 2,4-Dichloro-6-hydroxybenzaldehyde binds to both the inner membrane of mitochondria and to the plasma membrane of cancer cells, thereby inhibiting their function.Formule :C7H4Cl2O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :191.01 g/mol2,5-Dimethylbenzaldehyde
CAS :2,5-Dimethylbenzaldehyde is a chemical that is used in the synthesis of various compounds. It has been shown to have anticancer and energy metabolism properties. 2,5-Dimethylbenzaldehyde can be used as an energy source in the mitochondria. This compound also prevents the formation of fatty acids by inhibiting the conversion of acetyl-CoA into malonyl-CoA. The phase transition temperature for 2,5-dimethylbenzaldehyde is approximately −20 °C. The reaction mechanism for this compound is not well understood, but it has been shown to react with piperonal to form 3,4-dimethylbenzyl alcohol and methyl ethyl ether, which are both carcinogenic compounds. Chemical ionization mass spectrometry experiments have shown that protonated 2,5-dimethylbenzaldehyde reacts with methane gas to form methyl ethane and hydrogen gas. Thermodynamic data suggest that 2,5-dimethylFormule :C9H10ODegré de pureté :Min. 98.0 Area-%Couleur et forme :Slightly Yellow Clear LiquidMasse moléculaire :134.18 g/mol4-Hydroxybenzaldehyde
CAS :4-Hydroxybenzaldehyde is a phenolic compound that is produced in plants. 4-Hydoxybenzaldehyde is used as an extractant for sodium carbonate and hydroxyl group from acetate extract. The locomotor activity of animals was tested following administration of this substance, and it has been shown to have a high resistance against x-ray crystallography. The reaction mechanism for the formation of p-hydroxybenzoic acid from 4-hydroxybenzaldehyde has been proposed, which may be due to the oxidation of 4-hydroxybenzaldehyde by hydrogen peroxide. This reaction also induces apoptosis pathway in cells. Kinetic data for the reaction between 4-hydroxybenzaldehyde and hydrogen peroxide were obtained using UV spectroscopy.Formule :C7H6O2Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :122.12 g/mol2-fluoro-4-(trifluoromethyl)benzaldehyde
CAS :2-fluoro-4-(trifluoromethyl)benzaldehyde is a chemical compound that can be synthesized by the reaction of peroxide with fluorine. It is used as a solvent in coatings and in the production of organic chemicals. 2-fluoro-4-(trifluoromethyl)benzaldehyde has been shown to be toxic to cancer cells at high concentrations, but not normal cells. The waveguide effect can be observed at temperatures below -60°C and it has three functional groups that are hydrolyzed by HCl.Formule :C8H4F4ODegré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :192.11 g/mol(3E)-4-(1,3-Benzodioxol-4-yl)-3-butenoic acid
CAS :2,3-Methylenedioxybenzaldehyde is an organic compound that has been used as a chemical ionization reagent in the development of chemosensors. The formyl group in this molecule reacts with chloride to produce the corresponding formate salt, which can be detected by gas chromatography. This compound has also been shown to inhibit bacterial growth in vitro and may have potential applications as a drug substance. 2,3-Methylenedioxybenzaldehyde is an isomer of 2,4-methylenedioxybenzaldehyde, which has been shown to inhibit bacterial growth via hydrogen bonding with amines and electron deficient molecules such as chlorides. 2,3-Methylenedioxybenzaldehyde can be used for chromatographic science and the detection of drugs in urine samples.Formule :C11H10O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :206.19 g/mol5-(Trifluoromethoxy)salicylaldehyde
CAS :5-(Trifluoromethoxy)salicylaldehyde is a ligand that binds to the active site of the enzyme catalysis, thereby inhibiting its activity. It has been shown to be effective in colon cancer and other cancers due to its ability to inhibit protein synthesis. 5-(Trifluoromethoxy)salicylaldehyde also inhibits the production of prostaglandins, which may prevent inflammation. The compound is also used in supramolecular chemistry and biological studies as a tool for studying protein-ligand interactions. 5-(Trifluoromethoxy)salicylaldehyde has been shown to have dose-dependent effects on cell proliferation and protein synthesis.Formule :C8H5F3O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :206.12 g/mol4-Methoxy-2-methylbenzaldehyde
CAS :4-Methoxy-2-methylbenzaldehyde (4MMBA) is a synthetic chemical that is used as an antifungal agent. It interacts with the cellular membranes of fungi and disrupts their ability to maintain homeostasis. 4MMBA inhibits the growth of invasive aspergillosis by inhibiting protein synthesis, which leads to cell death. The mechanism of action for 4MMBA is not well understood, but it has been shown to inhibit the growth of fungi in a model system. It also inhibits the production of pyrylium, which may be responsible for its activity against fungi.Formule :C9H10O2Degré de pureté :90%Masse moléculaire :150.17 g/mol4-Methoxycinnamylidene acetaldehyde
CAS :4-Methoxycinnamylidene acetaldehyde is a versatile building block with a CAS number of 27394-81-6. It is used in the research and production of fine chemicals, pharmaceuticals, and high quality reagents. 4-Methoxycinnamylidene acetaldehyde can be used as a useful scaffold for the synthesis of complex compounds. This building block is also a useful intermediate in organic chemistry reactions.
Formule :C12H12O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :188.22 g/molGlycolaldehyde dimer
CAS :Glycolaldehyde dimer is a molecule that is the product of an intramolecular hydrogenation reaction. It has been shown to have estrogen receptor modulator activity, which may be due to its ability to bind to estrogen receptors and inhibit the production of inflammatory cytokines. Glycolaldehyde dimer also has the potential to be used as a therapeutic agent for inflammatory bowel disease. Glycolaldehyde dimer binds to crystalline cellulose and undergoes a series of chemical reactions, including hydrolysis by hydroxyl group, hydrochloric acid, and hydrogen bond. The logistic regression analysis shows that the molecule is more potent in rats with bowel disease than those without.Formule :C4H8O4Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :120.1 g/mol5-Methylnicotinaldehyde
CAS :5-Methylnicotinaldehyde is a chemical compound that belongs to the group of tetrahydropyridines. It is a reagent for producing triphosgene and dimethylformamide. 5-Methylnicotinaldehyde has been shown to inhibit muscarinic acetylcholine receptors, leading to an increase in acetylcholine release from nerve endings. This may be due to its ability to bind with the receptor affinity site at the base of the nicotinic acetylcholine receptor. 5-Methylnicotinaldehyde also has anti-inflammatory properties and can be used as a pesticide.
Formule :C7H7NODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :121.14 g/mol3,5-Dichloro-4-hydroxybenzaldehyde
CAS :3,5-Dichloro-4-hydroxybenzaldehyde is a triiodomethane derivative that reacts with chlorine to form a chlorinated aldehyde. It is used as an intermediate in the production of 4-hydroxybenzoic acid from phenylacetic acid and 4,4'-dichlorodiphenyl sulfone. 3,5-Dichloro-4-hydroxybenzaldehyde can be decarboxylated at elevated temperatures to produce formic acid. This compound has been used in wastewater treatment as it can remove chlorine byproducts and other pollutants such as nitrates, nitrites, and iron ions. The reaction kinetics of 3,5-dichloro-4-hydroxybenzaldehyde have been studied using hydroxymethyl groups and formyl groups to determine the rate of demethylation. The rates were found to be dependent on temperature.Formule :C7H4Cl2O2Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :191.01 g/mol3-Fluoro-4-hydroxybenzaldehyde
CAS :3-Fluoro-4-hydroxybenzaldehyde is a hydroxyl group with an activation energy of 87.7 kJ/mol. The molecule can be synthesized by the reaction of salicylaldehyde and 3,4-dihydroxybenzaldehyde in the presence of an organic solvent such as chloroform or methylene chloride. This compound has been shown to cause cell death in ht-29 cells and cancer cell lines, as well as human ovarian carcinoma cells. It causes apoptosis by inhibiting mitochondrial membrane potential, which leads to decreased intracellular ATP levels. 3-Fluoro-4-hydroxybenzaldehyde is most commonly used in molecular modeling studies to represent the hydroxyl group due to its simplicity in comparison to other hydroxyl groups like methanol or ethanol.Formule :C7H5FO2Degré de pureté :90%Couleur et forme :White PowderMasse moléculaire :140.11 g/mol2-Fluoro-6-methoxybenzaldehyde
CAS :2-Fluoro-6-methoxybenzaldehyde is a quinone that is used as an intermediate in the synthesis of other organic compounds. It has been shown to be a competitive inhibitor of malonate-induced fibrillation in heart muscle and also slows the reaction time. The pharmacokinetic properties of 2-fluoro-6-methoxybenzaldehyde have been evaluated in dogs, rats, and rabbits. In all three species, 2-fluoro-6-methoxybenzaldehyde showed no significant accumulation in any tissue after intravenous injection and was rapidly excreted unchanged in urine. 2-Fluoro-6-methoxybenzaldehyde may have some potential as an antihypertensive agent due to its ability to reduce blood pressure in rabbits.Formule :C8H7FO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :154.14 g/mol2-Carboxy-3,4-dimethoxybenzaldehyde
CAS :2-Carboxy-3,4-dimethoxybenzaldehyde is a chemical that belongs to the class of compounds known as butyric acid derivatives. It is a colorless liquid with a pungent odor and can be used in pharmaceutical preparations as an antispasmodic or a sedative. 2-Carboxy-3,4-dimethoxybenzaldehyde has been shown to have radical scavenging activities in tissue culture systems and dry weight reaction products in the presence of hydrochloric acid and chloride ion. This compound can also act as an acid complexing agent for hydrogen chloride and depressant activity on animal behavior.Formule :C10H10O5Degré de pureté :Min. 95%Couleur et forme :White Yellow PowderMasse moléculaire :210.18 g/mol
