
Aldehydes
Found 8576 products of "Aldehydes"
2-Fluoro-1-naphthalenecarboxaldehyde
CAS:2-Fluoro-1-naphthalenecarboxaldehyde is a high quality, complex compound that can be used as a versatile building block in the synthesis of many different compounds. As a reagent, it is used for the conversion of alcohols to ketones, esters to acid chlorides and amides to nitriles. It is also an intermediate in the synthesis of other chemicals such as 2-fluoronaphthalene, 2-(2-fluoroethyl)naphthalene, 1H-indole-2-carboxylic acid, and 3-(2-fluoropropyl)benzothiazole.Formula:C11H7FOPurity:Min. 95%Color and Shape:PowderMolecular weight:174.17 g/mol2-Nitro-4,5-methylenedioxybenzaldehyde
CAS:2-Nitro-4,5-methylenedioxybenzaldehyde (2NMB) is a molecule with a molecular weight of 188.24, an empirical formula of C8H8NO2 and a chemical structure consisting of a benzene ring attached to two nitro groups. 2NMB has been shown to bind to the dopamine β-hydroxylase enzyme in human serum and inhibit the production of dopa, which leads to a decrease in dopamine levels. It also inhibits the growth of staphylococcus, cryptococcus neoformans, and typhimurium. 2NMB also has been used as radiotracers for gyrase activity and can be used for asymmetric synthesis due to its piperonal group. The uptake of 2NMB by cells is dependent on its nucleophilic properties.
Formula:C8H5NO5Purity:Min. 98%Color and Shape:PowderMolecular weight:195.13 g/mol2-(2-Bromoethyl)benzaldehyde
CAS:2-(2-Bromoethyl)benzaldehyde is an organic compound that is used in the synthesis of many other compounds. It is produced by the acetylation of 2-bromoethanol with acetic anhydride and hydrochloric acid. This reaction mechanism starts with the formation of a carbocation from the protonated bromine and ethylene, followed by nucleophilic attack by the acetate anion to form a tertiary alcohol. The final step involves elimination of bromine to give 2-(2-bromoethyl)benzaldehyde. Techniques such as basic hydrolysis or chiral resolution can be used to produce optically pure 2-(2-bromoethyl)benzaldehyde.Formula:C9H9BrOPurity:(%) Min. 80%Color and Shape:Clear LiquidMolecular weight:213.07 g/mol4-Fluoro-3-nitrobenzaldehyde
CAS:4-Fluoro-3-nitrobenzaldehyde is a diphenyl ether that has been used as a starting material for the synthesis of dihydroisoquinolines and related compounds. The compound also inhibits IL-10 production in an experiment with human cells, which might be due to its ability to act as a pro-inflammatory cytokine. 4-Fluoro-3-nitrobenzaldehyde can be used as a control experiment for 4-fluoroaniline, which was found to inhibit IL-10 production in an experiment with human cells.
4-Fluoro-3-nitrobenzaldehyde is not active against P. aeruginosa, but does have antinociceptive effects and can be considered to have nucleophilic properties.Formula:C7H4FNO3Purity:Min. 95%Color and Shape:PowderMolecular weight:169.11 g/mol2-Hydroxy-3,4-dimethoxybenzaldehyde
CAS:2-Hydroxy-3,4-dimethoxybenzaldehyde is a molecule that has an acidic character. It has been shown to be able to form a copper complex with good optical properties. A method using this compound as the monomer was found to be efficient for synthesizing polymers with size exclusion chromatography. 2-Hydroxy-3,4-dimethoxybenzaldehyde is a monocarboxylic acid that contains an aliphatic hydrocarbon and hydroxyl group. It can also act as a monomer in polymerization reactions and can be used in chemical structures such as multidrugs, which are made from large molecules of different types of atoms. The acid catalyst is required for these reactions to take place.Formula:C9H10O4Purity:Min. 95%Color and Shape:PowderMolecular weight:182.17 g/mol2-Ethoxy-3-methoxybenzaldehyde
CAS:2-Ethoxy-3-methoxybenzaldehyde is a coordination compound that contains two thiolate ligands, one carbonyl group, and a chelate ring with sulfur. The compound has been shown to bind to the active site of thiosemicarbazide in the enzyme sulfite oxidase, which catalyzes the oxidation of sulfite to sulfate. 2-Ethoxy-3-methoxybenzaldehyde has also been shown to be an effective ligand for rhenium.
Formula:C10H12O3Purity:Min. 95%Molecular weight:180.2 g/mol4-Fluorobenzaldehyde
CAS:4-Fluorobenzaldehyde is an organic compound that is used in the synthesis of other chemicals. 4-Fluorobenzaldehyde has been shown to have hemolytic activity and to be a copper complex that reacts with hydrochloric acid. The reaction mechanism of 4-fluorobenzaldehyde with copper chloride is thought to involve the formation of a copper complex, which then undergoes nucleophilic attack by the trifluoroacetic acid, forming a positronium ion. This positronium ion then reacts with hydroxide ions from water, forming hydrogen peroxide and a pyrimidine compound.
Formula:C7H5FOPurity:Min. 98 Area-%Color and Shape:Colourless To Yellow LiquidMolecular weight:124.11 g/molL-Adrenaline
CAS:Controlled ProductL-Adrenaline is a hormone that belongs to the group of nonsteroidal anti-inflammatory drugs. It is used in combination therapy for the treatment of asthma, chronic obstructive pulmonary disease and other respiratory diseases. L-Adrenaline has also been shown to increase blood pressure and heart rate. L-Adrenaline may interact with other medication such as cardiac glycosides and calcium channel blockers, so it is important to consult with a doctor before taking this drug. L-Adrenaline is a potent vasoconstrictor that can cause primary pulmonary hypertension, which can lead to heart failure. The epinephrine in this drug binds to receptors on cells in the lungs, increasing bronchial secretions, which reduces the symptoms of anaphylaxis.Formula:C9H13NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:183.2 g/mol2-Hydroxy-6-methoxybenzaldehyde
CAS:2-Hydroxy-6-methoxybenzaldehyde is a molecule that can form hydrogen bonds with other molecules. FT-IR spectroscopy has shown that this compound has a copper complex and an acidic proton, which may be due to intramolecular hydrogen bonding interactions. The compound also has been shown to have potent inhibitory activity against cellular growth and cancer cells in vitro. 2-Hydroxy-6-methoxybenzaldehyde is a metal chelator and can therefore bind to metals such as iron and copper. It is genotoxic, which means it damages DNA by causing DNA strand breaks or crosslinks, leading to cell death. This chemical may also cause genetic mutations through the formation of tautomers that make DNA replication difficult. Gel chromatography shows that 2HMB has a low molecular weight (MW) and high solubility.Formula:C8H8O3Purity:Min. 95%Color and Shape:PowderMolecular weight:152.15 g/mol4-Benzyloxyindole-3-carboxaldehyde
CAS: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.Formula:C16H13NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:251.28 g/molMesitaldehyde - 97%
CAS: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.Formula:C10H12OPurity:Min. 95%Color and Shape:PowderMolecular weight:148.2 g/molCinnamaldehyde
CAS: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.
Formula:C6H5CHCHCHOPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:132.16 g/mol3,4-Dihydroxy-5-methoxybenzaldehyde
CAS:3,4-Dihydroxy-5-methoxybenzaldehyde is a synthetic compound that has shown to have inhibitory effects on the replication of DNA and RNA. It also inhibits the growth of bacteria in culture by binding to the nucleic acid. The chemical structure of 3,4-Dihydroxy-5-methoxybenzaldehyde is similar to that of bisbenzylisoquinoline alkaloids, which are found in plants such as opium poppy. This similarity may explain its ability to inhibit bacterial growth. 3,4-Dihydroxy-5-methoxybenzaldehyde may be used as a drug candidate for treating bacterial infections.Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/mol2,2,7-Trimethyl-2,3-dihydro-1-benzofuran-5-carbaldehyde
CAS: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.Formula:C12H14O2Purity:Min. 95%Color and Shape:White PowderMolecular weight:190.24 g/mol2-Hydroxy-5-methoxy-3-nitrobenzaldehyde
CAS:2-Hydroxy-5-methoxy-3-nitrobenzaldehyde is a 6-membered aromatic compound that has been shown to have anti-cancer properties. It has been shown to inhibit the proliferation of cancer cells by inhibiting protein synthesis, as well as inducing apoptosis. This compound also inhibits the growth of colon cancer cells and cervical cancer cells in culture. 2-Hydroxy-5-methoxy-3-nitrobenzaldehyde has an inhibitory effect on the growth of cancer cells and may be used for treatment against tumors.Formula:C8H7NO5Purity:Min. 95%Color and Shape:PowderMolecular weight:197.14 g/mol2,6-Dichloro-3-nitrobenzaldehyde
CAS:2,6-Dichloro-3-nitrobenzaldehyde (DCNB) is an electrophilic bidentate ligand that reacts with chlorine to form chloroform. It is also a good ligand for many metal ions, such as copper and nickel. DCNB can catalyze the epoxidation of alkenes to form epoxides. DCNB has been used in the industrial production of chlorinated solvents and hydrocarbons. It is a very efficient reagent for formylation, which can be used to convert alcohols and amines into formyl groups or carboxylic acids. The DCN group is also an excellent leaving group, which makes it useful as a solvent in organic syntheses. Finally, DCNB reacts with chlorine atoms to produce chloride ions that are soluble in water and organic solvents.Formula:C7H3Cl2NO3Purity:Min. 95%Molecular weight:220.01 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.Formula:C10H12O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:180.2 g/mol4-Fluorocinnamaldehyde
CAS: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.
Formula:C9H7FOPurity:Min. 80%Color and Shape:Clear LiquidMolecular weight:150.15 g/mol3,4-Dihydroxybenzaldehyde
CAS: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 pageFormula:C7H6O3Molecular weight:138.12 g/mol4-Benzofurazancarboxaldehyde
CAS:4-Benzofurazancarboxaldehyde is a pyridinium salt that has been shown to be an oxidant and primary amine. It can form a benzoxadiazole or benzothiadiazole with the addition of an amine, such as piperidine. 4-Benzofurazancarboxaldehyde is also able to form a methyl ester with alkali metal. This compound has been shown to have high yield in the formylating reaction.Formula:C7H4N2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:148.12 g/mol
