
Aldehydes
Aldehydes are organic compounds containing a carbonyl group (C=O) bonded to at least one hydrogen atom. These versatile compounds are fundamental in various chemical reactions, including oxidation, reduction, and nucleophilic addition. Aldehydes are essential building blocks in the synthesis of pharmaceuticals, fragrances, and polymers. At CymitQuimica, we provide a diverse selection of high-quality aldehydes to support your research and industrial applications.
Found 8551 products of "Aldehydes"
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4-Benzyloxy-3-methoxybenzaldehyde
CAS:<p>4-Benzyloxy-3-methoxybenzaldehyde is a deuterium isotope analog of the natural compound benzaldehyde. This molecule has been shown to inhibit the growth of cancer cells in tissue culture by binding to DNA. The molecular mechanism of this inhibition is believed to involve an enzymatic process that results in the substitution of chloride for chlorine, thereby inhibiting DNA synthesis and preventing cell division. 4-Benzyloxy-3-methoxybenzaldehyde also inhibits the production of growth factors and thus has anticancer activity.</p>Formula:C15H14O3Purity:Min. 95%Color and Shape:PowderMolecular weight:242.27 g/mol6-Methoxy-2-naphthaldehyde
CAS:<p>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 dehydrogen</p>Formula:C12H10O2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:186.21 g/mol4-Fluoro-1H-indole-3-carbaldehyde
CAS:<p>4-Fluoro-1H-indole-3-carbaldehyde is a chemical compound that can be used as a reagent, reaction component, or building block in the synthesis of more complex compounds. This chemical is also known as CAS No. 23073-31-6 and has high quality and purity. 4-Fluoro-1H-indole-3-carbaldehyde is useful for research purposes and can be used as a speciality chemical or a fine chemical.</p>Formula:C9H6FNOPurity:Min. 95%Color and Shape:Yellow To Brown SolidMolecular weight:163.15 g/mol2,6-Dichloro-4-hydroxybenzaldehyde
CAS:<p>2,6-Dichloro-4-hydroxybenzaldehyde is a chlorinated organic compound that can be synthesized by the chlorination of 2,6-dichlorobenzaldehyde. It has non-polar properties and can be used as an analytical reagent. Due to its chlorine atoms, it is used in the analysis of chlorine content in water and other substances. It is a formyl derivative and a homologue of formaldehyde. There are two isomers: 2,4-dichloro-6-hydroxybenzaldehyde (2,4 DCHA) and 2,5-dichloro-6-hydroxybenzaldehyde (2,5 DCHA).</p>Formula:C7H4Cl2O2Purity:Min. 95%Color and Shape:Yellow PowderMolecular weight:191.01 g/mol3-Bromo-4,5-dimethoxybenzaldehyde
CAS:<p>3-Bromo-4,5-dimethoxybenzaldehyde is a molecule that is acidic in nature. It inhibits phosphatases and has shown cytotoxic activity against cancer cells in vitro. This compound also has antibacterial properties and can be used to treat bacterial infections. 3-Bromo-4,5-dimethoxybenzaldehyde is also a synthetic compound that can be found in the bisbenzylisoquinoline alkaloids family. It has been shown to have anti-tumor activity as well as an interaction with aldehydes and chalcones, which may lead to anti-inflammatory effects.</p>Formula:C9H9BrO3Purity:Min. 95%Color and Shape:PowderMolecular weight:245.07 g/mol1-Methyl-1H-imidazole-4-carbaldehyde
CAS:<p>1-Methyl-1H-imidazole-4-carbaldehyde is an Imidazole derivative. Imidazoles are the most prominent heterocyclic scaffolds found in medical molecules and natural products. Due to the peculiar structural characteristics of imidazole, it is advantageous for imidazole groups to combine with various receptors and enzymes in biological systems, through diverse weak interactions. 1-Methyl-1H-imidazole-4-carbaldehyde is one of many imidazole derivatives that are used as building blocks for a wide variety of target compounds.</p>Formula:C5H6N2OPurity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:110.11 g/mol(3E)-4-(1,3-Benzodioxol-4-yl)-3-butenoic acid
CAS:<p>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.<br>2,3-Methylenedioxybenzaldehyde can be used for chromatographic science and the detection of drugs in urine samples.</p>Formula:C11H10O4Purity:Min. 95%Color and Shape:PowderMolecular weight:206.19 g/molImidazole-2-carboxaldehyde
CAS:<p>Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins.</p>Formula:C4H4N2OPurity:Min. 98 Area-%Color and Shape:Slightly Yellow PowderMolecular weight:96.09 g/molGallaldehyde
CAS:<p>Gallaldehyde is a bioactive phenolic compound with antiproliferation activity. It has been shown to inhibit the growth of bacteria in vitro and also has hypoglycemic effects in mice. Gallaldehyde inhibits tyrosine kinase activity, which is needed for the growth of cells. Gallaldehyde is a tannin that can bind to proteins, inhibiting their functions. Gallaldehyde may also have anti-inflammatory properties due to its ability to inhibit the production of TNF-α induced by epidermal growth factor. This active form is metabolized by a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid.</p>Formula:C7H6O4Purity:Min. 95%Color and Shape:PowderMolecular weight:154.12 g/mol2,3-Dichlorobenzaldehyde oxime
CAS:<p>2,3-Dichlorobenzaldehyde oxime is a versatile building block and reagent in the synthesis of complex compounds. It is mainly used as a research chemical and speciality chemical. 2,3-Dichlorobenzaldehyde oxime has been widely used for the preparation of fine chemicals, pharmaceuticals, agrochemicals, and other organic compounds. This compound can be reacted with various reagents to produce useful scaffolds or reaction components.</p>Formula:C7H5Cl2NOPurity:Min. 95%Color and Shape:PowderMolecular weight:190.03 g/molZ-Phe-Tyr-aldehyde
CAS:<p>Z-Phe-Tyr-aldehyde is a natural compound that inhibits the activity of cathepsin, an enzyme associated with cancer and bowel disease. The compound also inhibits the expression of covid-19, which is a protein that regulates cell death. Z-Phe-Tyr-aldehyde has been shown to cause caspase-independent cell death in human leukemia cells. This compound also blocks the TLR4 receptor, which is thought to play a role in infectious diseases such as SARS and Covid-2. It has been found to inhibit protein synthesis in bacteria, which may be due to its ability to inhibit ribosomal function.</p>Formula:C26H26N2O5Purity:Min. 95%Molecular weight:446.5 g/mol2,2,7-Trimethyl-2,3-dihydro-1-benzofuran-5-carbaldehyde
CAS:<p>2,2,7-Trimethyl-2,3-dihydro-1-benzofuran-5-carbaldehyde is a fine chemical that is used as a building block in research and synthesis of other chemicals. It has been shown to be a versatile building block for the synthesis of complex compounds. 2,2,7-Trimethyl-2,3-dihydro-1-benzofuran-5-carbaldehyde is also a useful intermediate to make other chemicals as well as a reagent in the production of speciality chemicals. This compound can be used in reactions with amines and alcohols. It has been found to have high quality that makes it useful for use in reactions with DNA and RNA nucleotides and proteins.</p>Formula:C12H14O2Purity:Min. 95%Color and Shape:White PowderMolecular weight:190.24 g/mol4-Iodobenzaldehyde
CAS:<p>4-Iodobenzaldehyde is a chemical compound with the molecular formula C6H5IO. It is an aromatic compound that can be used in cancer therapy. 4-Iodobenzaldehyde reacts with trifluoroacetic acid to form an intramolecular hydrogen, which is detected using a low-energy monomer and high detection sensitivity. 4-Iodobenzaldehyde has two phenyl substituents and a serine protease functional group, which are required for its interaction with other molecules. The presence of these functional groups allows analytical methods to be used to identify 4-iodobenzaldehyde in various samples. Using analytical methods, it can be determined that 4-iodobenzaldehyde interacts with an acceptor molecule at the reaction vessel thermally or by irradiation.</p>Formula:C7H5IOPurity:Min. 95%Color and Shape:Yellow PowderMolecular weight:232.02 g/molHexoprenaline sulphate
CAS:<p>β-adrenoreceptor agonist; betamimetic agent</p>Formula:C22H34N2O10SPurity:Min. 95%Color and Shape:White PowderMolecular weight:518.58 g/mol2-Fluoro-6-nitrobenzaldehyde
CAS:<p>2-Fluoro-6-nitrobenzaldehyde is an electron donor that reduces a range of electron acceptors including piperazine. This compound has been shown to have antitumor effects. 2-Fluoro-6-nitrobenzaldehyde has also been shown to inhibit the growth of cancer cells in vitro and in vivo. The mechanism of action is not yet known, but it is thought that 2-fluoro-6-nitrobenzaldehyde may be a potential chemotherapeutic agent for pancreatic cancer therapy.</p>Formula:C7H4FNO3Purity:Min. 95%Color and Shape:PowderMolecular weight:169.11 g/mol2-(4-Fluorophenyl)thiazole-4-carbaldehyde
CAS:<p>Please enquire for more information about 2-(4-Fluorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C10H6FNOSPurity:Min. 95%Color and Shape:PowderMolecular weight:207.23 g/mol2,4-Dichloro-5-fluorobenzaldehyde
CAS:<p>2,4-Dichloro-5-fluorobenzaldehyde (2,4-DFCA) is a functional group that can be found in inorganic, fatty acids, and fatty acid. 2,4-DFCA has been shown to increase insulin-like growth factor I (IGF-I) levels in vitro and in vivo. 2,4-DFCA also increases the expression of IGF-I gene polymorphisms. This compound is used to induce insulin resistance by increasing serum level of IGF-I. 2,4-DFCA also inhibits the activity of a protein called impeller that is required for cardiac contractility. This compound can be found on the surface of untreated control cells.</p>Formula:C7H3Cl2FOPurity:Min. 95%Color and Shape:PowderMolecular weight:193 g/moltrans-Cinnamaldehyde
CAS:<p>Cinnamaldehyde is a natural compound that has shown to have antiviral and antimicrobial properties. It has been shown to inhibit the toll-like receptor, which is a protein on the surface of cells that detects bacteria and other microorganisms. Cinnamaldehyde is also able to inhibit c. glabrata growth in vitro at concentrations between 10 and 100 μM, as well as copper-mediated cell death in hl-60 cells. Cinnamaldehyde has been shown to cause neuronal death by interfering with cellular physiology. This compound can be used in the treatment of infectious diseases because it inhibits bacterial dna gyrase, dna topoisomerase, and rna synthesis.</p>Formula:C9H8OPurity:Min. 95%Color and Shape:PowderMolecular weight:132.16 g/mol3-Methoxy-4-(4-nitrobenzyloxy)benzaldehyde
CAS:<p>3-Methoxy-4-(4-nitrobenzyloxy)benzaldehyde is a chemical intermediate that is used in the synthesis of complex compounds. It has been shown to be an effective reagent for the synthesis of various organic compounds, such as pharmaceuticals and pesticides. 3-Methoxy-4-(4-nitrobenzyloxy)benzaldehyde is also used as a research chemical or as a speciality chemical in laboratories. This compound can be used as a building block in the synthesis of other compounds with interesting properties, such as 3-methoxy-4-(2,5-dichlorobenzyloxy)benzaldehyde.</p>Formula:C15H13NO5Purity:Min. 95%Color and Shape:PowderMolecular weight:287.27 g/mol2-Nitrobenzaldehyde
CAS:<p>2-Nitrobenzaldehyde is a nitro compound that reacts with the intramolecular hydrogen of an alkene to form a nitroalkane. It is used as an antimicrobial agent, in which it inhibits the growth of bacteria by reacting with the intermolecular hydrogen bonding in the bacterial cell membrane. In addition, 2-Nitrobenzaldehyde has been shown to inhibit fatty acid synthesis and transfer reactions. The optimum concentration for this chemical is 0.01% to 0.1%. This chemical is soluble in both water and organic solvents, such as methanol and ethanol.</p>Formula:C7H5NO3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:151.12 g/mol
