
Aldeídos
Os aldeídos são compostos orgânicos que contêm um grupo carbonila (C=O) ligado a pelo menos um átomo de hidrogênio. Esses compostos versáteis são fundamentais em várias reações químicas, incluindo oxidação, redução e adição nucleofílica. Os aldeídos são building blocks essenciais na síntese de produtos farmacêuticos, fragrâncias e polímeros. Na CymitQuimica, oferecemos uma ampla seleção de aldeídos de alta qualidade para apoiar suas aplicações de pesquisa e industriais.
Foram encontrados 8573 produtos de "Aldeídos"
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3,5-Dibromobenzaldehyde
CAS:<p>3,5-Dibromobenzaldehyde is an analytical reagent that has been used as a chemosensor. The compound was synthesized by the reaction of benzaldehyde with bromine and potassium hydroxide (KOH). 3,5-Dibromobenzaldehyde has a skeleton consisting of three phenyl groups and two aldehyde groups. The compound also contains two active methylene groups and two vinylene groups. 3,5-Dibromobenzaldehyde can be detected by fluorescence probe or low energy electron diffraction. This chemical is an effective antibacterial agent with an LD50 value of 1.6 milligrams per kilogram in rats.</p>Fórmula:C7H4Br2OPureza:Min. 95%Cor e Forma:White PowderPeso molecular:263.91 g/molMesitaldehyde - 97%
CAS:<p>Mesitaldehyde is a diazonium salt that is synthesized by the reaction of nitrosyl chloride and sodium carbonate in an acidic solution. This chemical has been studied for its potential use as a therapeutic drug due to its ability to inhibit the enzyme dpp-iv, which is involved in the development of diabetic neuropathy. Mesitaldehyde has also been shown to be an inhibitor of malonic acid, ethylmalonic acid and other organic acids. The analytical method for mesitaldehyde involves hydrolyzing the product with hydrochloric acid in order to produce ethylmalonic acid, which can then be quantified using spectrophotometry.</p>Fórmula:C10H12OPureza:Min. 95%Cor e Forma:PowderPeso molecular:148.2 g/mol3-Nitro-4-chlorobenzaldehyde
CAS:<p>3-Nitro-4-chlorobenzaldehyde is a copper complex that has been used in the study of molecular interactions. The molecule has been studied by a number of techniques, including binding experiments, vibrational spectroscopy, and light emission. 3-Nitro-4-chlorobenzaldehyde has shown bacteriostatic activity against Escherichia coli and Bacillus subtilis. This compound also appears to have potential as a drug target due to its ability to inhibit the growth of Pseudomonas aeruginosa. 3-Nitro-4-chlorobenzaldehyde may be useful in the treatment of industrial processes involving nitric acid.</p>Fórmula:C7H4ClNO3Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:185.56 g/mol4-Benzyloxyindole-3-carboxaldehyde
CAS:<p>4-Benzyloxyindole-3-carboxaldehyde is an analog of psilocin that is synthesized by the condensation of formylbenzene with indole-3-carboxaldehyde. It has been shown to act as a formylating agent, which can be used in the synthesis of other compounds. 4-Benzyloxyindole-3-carboxaldehyde may also be converted to n-dimethyltryptamine (DMT) by oxidation and decarboxylation.</p>Fórmula:C16H13NO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:251.28 g/mol2-Hydroxy-3-methoxybenzaldehyde
CAS:<p>2-Hydroxy-3-methoxybenzaldehyde is a model compound that is used to study the reaction mechanism of hydrogen bonding. It has been shown to have antioxidative properties and amoebicidal activity. The biological properties of 2-hydroxy-3-methoxybenzaldehyde are still being studied. There are also no reports on its toxicity or carcinogenicity in humans. This compound is a member of the group P2, which includes compounds with two aromatic rings connected by one carbon atom. The molecular geometry around this carbon atom is pyramidal and the molecule can exist in either an axial or equatorial orientation. Synchronous fluorescence experiments have shown that 2-hydroxymethoxybenzaldehyde reacts with Toll-like receptor 4 (TLR4).</p>Fórmula:C8H8O3Pureza:Min. 95%Cor e Forma:Yellow PowderPeso molecular:152.15 g/mol3,4-Dihydroxybenzaldehyde
CAS:<p>Please enquire for more information about 3,4-Dihydroxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C7H6O3Peso molecular:138.12 g/mol4-N-Octylbenzaldehyde
CAS:<p>4-N-Octylbenzaldehyde is a nitro compound which is used as an immunosuppressive agent. It has been shown to inhibit the activity of diphenolase, which plays an important role in the metabolism of fatty acids. 4-N-Octylbenzaldehyde also has an oil extractant that can be used to extract and separate different types of organic compounds from oils, fats, or greases. In addition, 4-N-octylbenzaldehyde inhibits the synthesis of prostaglandin E2 and thromboxane A2 by inhibiting cyclooxygenase enzymes. It has been shown to possess anti-inflammatory properties and has been found to be useful in treating rheumatoid arthritis.</p>Fórmula:C15H22OPureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:218.33 g/mol4-Cyano-2-hydroxybenzaldehyde
CAS:<p>4-Cyano-2-hydroxybenzaldehyde is a high quality chemical that can be used as a reagent and intermediate in the synthesis of complex compounds. It is also an important building block in the synthesis of fine chemicals. 4-Cyano-2-hydroxybenzaldehyde has been used as a versatile building block in the synthesis of organic compounds, useful scaffolds in medicinal chemistry, and reactive intermediates. It has also been shown to have anti-inflammatory properties and may be a potential treatment for inflammatory bowel disease.</p>Fórmula:C8H5NO2Pureza:Min. 95%Peso molecular:147.13 g/mol3-Bromo-4-methoxybenzaldehyde
CAS:<p>3-Bromo-4-methoxybenzaldehyde is a heterocycle that contains a covalent inhibitor. It has been shown to have inhibitory activity against imines, hydroxyl groups, and human serum. 3-Bromo-4-methoxybenzaldehyde has been shown to be an efficient method for the synthesis of nitrogen containing heterocycles with potential use as pharmaceuticals. This compound has also been used in the asymmetric synthesis of diphenyl ethers, which are useful in pharmacological studies. The reaction mechanism of this compound is not well understood and needs more research before it can be applied to other areas.</p>Fórmula:C8H7BrO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:215.04 g/mol2-Carbomethoxybenzaldehyde
CAS:<p>2-Carbomethoxybenzaldehyde (2CMB) is a synthetic chemical compound that has been used as an efficient method for the synthesis of amines. The carbonyl group in 2CMB reacts with nucleophiles, such as amines, to form a tetrahydroisoquinoline derivative. This nucleophilic attack leads to the formation of an unstable intermediate that can be isolated and purified by trifluoroacetic acid (TFA). 2CMB is also used in the synthesis of quinoline derivatives and naphthalene derivatives. The acidic properties of 2CMB allow it to react with carboxylic acids, leading to the formation of esters.</p>Fórmula:C9H8O3Pureza:Min. 95%Cor e Forma:Colorless PowderPeso molecular:164.16 g/mol2-Fluoro-6-methoxybenzaldehyde
CAS:<p>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.</p>Fórmula:C8H7FO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:154.14 g/mol5-Bromo-3,4-dihydroxybenzaldehyde
CAS:<p>5-Bromo-3,4-dihydroxybenzaldehyde (5BDBA) is a chemical compound that can be used as a reactive dye and photochemical crosslinker in the preparation of polymers. 5BDBA has been shown to have chemoattractant properties for immune cells, such as activated T lymphocytes and neutrophils. It also has been shown to have an effect on β-cells in the pancreas and skin cells. This compound has been found to activate the nuclear factor kappa-light-chain enhancer (NFκB), which leads to increased expression of chemoattractant protein (MCP). In 3T3-L1 preadipocytes, 5BDBA has been shown to induce accumulation of fatty acids by activating peroxisome proliferator activator receptor gamma.</p>Fórmula:C7H5BrO3Pureza:Min. 95%Cor e Forma:Yellow PowderPeso molecular:217.02 g/mol2-Methylveratraldehyde
CAS:2-Methylveratraldehyde is a chiral compound that can be used as a reagent in organic synthesis. It has been shown to be a potentiator of the antimicrobial activity of grignard reagents and carbonation, which are chemical reactions that form new carbon-carbon bonds. 2-Methylveratraldehyde also has biological studies, such as its use as an inducer of phytoalexin production in plants.Fórmula:C10H12O3Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:180.2 g/molCinnamaldehyde
CAS:<p>Cinnamaldehyde is an aldehyde that occurs naturally in plants such as cinnamon, apples, and cumin. It is used as a flavoring agent for foods and beverages, as well as in perfumes. Cinnamaldehyde has been shown to have minimal toxicity and minimal mutagenic or carcinogenic potential. This compound has been shown to exhibit antimicrobial activity against bacteria by inhibition of bacterial cell growth through inhibition of the synthesis of proteins essential for cell division. Cinnamaldehyde also exhibits anti-inflammatory properties by inhibiting prostaglandin synthesis. The antimicrobial effects of cinnamaldehyde are due to its ability to bind to the enzyme alcohol dehydrogenase, which prevents the conversion of alcohols into aldehydes. Cinnamaldehyde can be found in many natural compounds such as cinnamic acid and eugenol.</p>Fórmula:C6H5CHCHCHOPureza:Min. 95%Cor e Forma:Colorless Clear LiquidPeso molecular:132.16 g/mol7-Benzyloxindole-3-carboxaldehyde
CAS:<p>7-Benzyloxindole-3-carboxaldehyde (BXA) is an assembled molecule that can be synthesized in a scalable and catalytic manner. BXA is an unwanted product that arises from the reaction of 7-benzyloxyindole with adrenaline. The hydrogenolysis of BXA yields the enantiomeric 7-benzyloxyindole, which has been shown to possess anti-inflammatory properties. When debenzylated by hydrogenolysis, crystallization of the byproduct is observed.</p>Fórmula:C16H13NO2Pureza:Min. 95%Peso molecular:251.28 g/mol3-Chloro-2-nitrobenzaldehyde
CAS:<p>3-Chloro-2-nitrobenzaldehyde is an analog of 2-nitrobenzaldehyde. It can be synthesized by reacting a halogen with benzaldehyde, such as chlorine or bromine. 3-Chloro-2-nitrobenzaldehyde is unreactive and can be used in the production of other compounds, such as pharmaceuticals. 3-Chloro-2-nitrobenzaldehyde has been shown to react with sodium methoxide to produce a methoxide. The methoxide is then reacted with an alcohol to produce an ester.</p>Fórmula:C7H4ClNO3Pureza:Min. 95%Peso molecular:185.56 g/mol4-Fluorocinnamaldehyde
CAS:<p>4-Fluorocinnamaldehyde is a reactive molecule that can be used in the catalytic asymmetric synthesis of 4-fluoroalkylbenzenes, which are used as intermediates in the production of pharmaceuticals. It reacts with hydroxymethyl groups to form 4-fluoroalkylbenzene derivatives, which are substrates for asymmetric reactions. This compound has been shown to react with amines and thiols to form Michael acceptors and Michael donors respectively. The crystallographic data obtained from this molecule shows that it belongs to space group P2 and its crystal system is orthorhombic. It also has optical properties that make it suitable for use as an optical material or nanowires.</p>Fórmula:C9H7FOPureza:Min. 80%Cor e Forma:Clear LiquidPeso molecular:150.15 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>Fórmula:C4H4N2OPureza:Min. 98 Area-%Cor e Forma:Slightly Yellow PowderPeso molecular:96.09 g/molCyclooctanecarbaldehyde
CAS:Cyclooctanecarbaldehyde is a reactive chemical that contains a hydroxyl group and hydroxy group. It is used for the production of polymers such as cyclooctyne-1,4-diol. Cyclooctanecarbaldehyde is also used to synthesize acyl halides. The compound has been shown to be cytotoxic in cancer cells. It can inhibit the production of nucleic acids, proteins and lipids in cancer cells, leading to cell death. Cyclooctanecarbaldehyde also has depression and cardiac arrhythmia effects due to its κ-opioid receptor agonist properties.Fórmula:C9H16OPureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:140.22 g/mol5-Methylindole-3-carboxaldehyde
CAS:<p>5-Methylindole-3-carboxaldehyde (5MI) is a β-unsaturated aldehydes that is used as an analyte in assays for the detection of α,β-unsaturated aldehydes. It has been shown to be effective in degranulation of cells and induces cellular degranulation. 5MI has also been shown to be an analog of other β-unsaturated aldehydes and acts competitively with these compounds.</p>Fórmula:C10H9NOPureza:Min. 95%Cor e Forma:PowderPeso molecular:159.18 g/mol
