Aldehydes

<p>4-Bromo-3,5-dimethoxybenzaldehyde is a compound that inhibits the replication of cells. It has been shown to induce apoptosis and inhibit tumor growth, including skin tumors and malignant melanoma cells. This chemical is synthesized by reacting an acrylonitrile with sodium hydroxide in a biphenyl amide. 4-Bromo-3,5-dimethoxybenzaldehyde has been used to inhibit bacterial growth, but it is not active against Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>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.</p>

<p>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.</p>

<p>3-Methoxy-4-methylbenzaldehyde is a chemical compound that belongs to the class of phenylpropanoids. It has been shown to have a variety of uses, including as a drug substance and in natural products. 3-Methoxy-4-methylbenzaldehyde can be used for labeling, mass spectrometric detection, physicochemical techniques, and chromatographic science. The compound can be detected using electron ionization, mass spectrometric detection, or chromatographic science. Isomers of this compound are often difficult to identify due to the presence of other similar compounds.</p>

<p>2,4,6-Trimethoxybenzaldehyde is a chemical compound that is used as an intermediate in organic chemistry. It has been shown to have antiviral effects on influenza A virus by inhibiting the enzyme neuraminidase. This inhibition prevents the release of viruses from infected cells and thus prevents viral replication. 2,4,6-Trimethoxybenzaldehyde also inhibits the growth of cancer cells in vitro and has minimal toxicity to normal cells. This chemical has been shown to inhibit the reaction mechanism of proton pumps in mammalian cells, which may be due to its ability to inhibit p2y receptors or nitrogen atoms. 2,4,6-Trimethoxybenzaldehyde can also be used as a solvent for pharmaceutical preparations and as a reagent in x-ray diffraction data analysis.</p>

<p>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.</p>

<p>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.</p>

<p>3-Cyclohexene-1-carboxaldehyde is a carbonyl reduction agent that converts primary alcohols to aldehydes. 3-Cyclohexene-1-carboxaldehyde is an effective catalyst for the reduction of alpha, beta unsaturated carbonyls. The mechanism of this reaction involves the elimination of hydrogen chloride, which forms hydrochloric acid. The reaction can be controlled by adding either alkali metal or chloride ions to the reaction mixture. This process produces 2 products: aldehyde and alkyl chlorides. 3-Cyclohexene-1-carboxaldehyde is primarily used in the production of polyethylene terephthalate (PET) and nylon 6,6 from ethylene glycol.</p>

<p>Intermediate in organic synthesis</p>

<p>3-Hydroxybenzaldehyde (3HBA) is an organic molecule that belongs to the group of substituted benzaldehydes. It has been shown to induce muscle cell proliferation in vitro and in vivo, as well as increased levels of activated caspase-3 in vitro. 3HBA also has a high resistance to hydrochloric acid, hydrogen bond, and chemical structures. It also shows properties of intramolecular hydrogen bonding and aldehyde groups. 3HBA has been shown to be active against malonic acid-induced pulmonary edema in rats, which may be due to its ability to inhibit the release of erythrocytes from the bone marrow into the circulation.</p>

<p>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.</p>

<p>2-Furaldehyde dimethylacetal is a monomer with a hydroxyl group and an aldehyde group in the molecule. It is produced by the reaction of formaldehyde with methanol and sodium hydroxide, which react to create formaldehyde hemiacetal. The formaldehyde hemiacetal then reacts with methanol to produce 2-furaldehyde dimethylacetal. This compound has been shown to polymerize when heated or irradiated with ultraviolet light, forming polymers. Gel chromatography can be used to separate this compound from other compounds in a mixture. The molecular weight of 2-furaldehyde dimethylacetal is 186g/mol.</p>

<p>4-Bromo-3-methylbenzaldehyde is a versatile building block that is used in the synthesis of many complex compounds. It can be used as a reactant, reagent, or speciality chemical. 4-Bromo-3-methylbenzaldehyde is an intermediate for the production of other chemicals and has been shown to be useful in the synthesis of various scaffolds. This product has been shown to have high purity and quality.</p>

<p>5-[(4,5-Dimethyl-4H-1,2,4-triazol-3-yl)thio]-2-furaldehyde is a versatile building block that can be used as a research chemical or reagent. It is also useful for the synthesis of complex compounds. This material has been shown to be an excellent starting point for the synthesis of high quality and useful scaffolds.</p>

<p>Please enquire for more information about 2-(3-Chlorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methoxybenzaldehyde oxime is a synthetic amine that is used in the synthesis of peroxides. The reaction rate and nature depend on the type of peroxide being synthesized, but typically, it is used with acetonitrile as a solvent and an acid catalyst. 2-Methoxybenzaldehyde oxime reacts with peracid to create an aldoxime and nitrite. This product can also be made by reacting benzaldehyde with nitrous acid, which will produce dioxane as an intermediate. The reaction time for this process takes about four hours at room temperature.</p>

<p>3-Methoxy-4,5-methylenedioxybenzaldehyde (MMDA) is an amine that is used in the synthesis of drugs and pharmaceuticals. It is a major component of myristicin, which is found in nutmeg. MMDA can be synthesized from aluminium chloride, hydrochloric acid and pyridine. The molecule has a skeleton that is recemic at acidic pH values and mesoionic at basic pH values. This compound also reacts with acetyl chloride to form 3,4-dimethoxyacetophenone, which can be chromatographically separated from other compounds. The chromatography produces flavonoid derivatives such as quercetin, 3′-methoxyquercetin and 3′,4′-dimethoxyquercetin. Flavonoids are polyphenolic compounds found in plants that have antioxidant properties. Chromatographic separation of these compounds can be done using spectrometric methods to</p>

<p>3,4,5-Trihydroxybenzaldehyde monohydrate is a chemical compound that belongs to the class of aromatic hydrocarbons. It has been shown to have a neurotoxic effect on the mouse brain and is used in the diagnosis of neurological diseases. 3,4,5-Trihydroxybenzaldehyde monohydrate is also used as an intermediate in the synthesis of other chemicals. The molecular formula for this substance is C9H7O3 and it contains three nitrogen atoms. The molecular weight is 179.06 g/mol and its sequence length is 707 amino acids long. This substance has been found to be present in humans with chronic kidney disease and insulin resistance.</p>

<p>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.</p>

<p>4'-Chloro-[1,1'-biphenyl]-4-carbaldehyde (CBA) is an intermediate in the synthesis of oritavancin. CBA is obtained by condensation of benzyl chloride and aldehydes. It is also used as a precursor to other compounds. In the laboratory, it can be obtained by heating an ether with chloroform in the presence of acid. 4'-Chloro-[1,1'-biphenyl]-4-carbaldehyde has been shown to be toxic, selective and efficient for certain reactions.</p>

<p>4-Acetamidobenzaldehyde is an organic compound that has been shown to exhibit inhibitory effects on influenza virus replication in cell culture. 4-Acetamidobenzaldehyde is a dihedral molecule with a p2 group and can be synthesized from benzaldehyde and acetamide. It has also been shown to have potential use in the treatment of tuberculosis. The biological properties of 4-acetamidobenzaldehyde are not well understood, but it is thought that uptake may occur through the imine nitrogen. This molecule has been detected in tissue samples such as lung, liver, and kidney.</p>

<p>6-Methyl-1H-indole-3-carbaldehyde is a synthetic chemical that has been used as a reagent in the form of its sodium salt. It is an acetylating agent and can be used for formylation reactions. 6-Methyl-1H-indole-3-carbaldehyde has shown strong antifungal activity against phytopathogenic fungi such as Fusarium, Rhizoctonia, and Phytophthora. This chemical also has a triazine group, which can be used to enhance the herbicidal properties of certain compounds.</p>

<p>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.</p>

<p>4-(Trifluoromethoxy)benzaldehyde is a chemical compound that is a substrate for tyrosinase and an inhibitor of the enzyme. It is also an anticancer compound that can be used to inhibit tumor growth by inhibiting protein synthesis. 4-(Trifluoromethoxy)benzaldehyde has been shown to have potent tyrosinase inhibition activity in vitro and in vivo, as well as binding activities with the CB2 receptor. This chemical has also been shown to inhibit virus replication, including HIV-1, and tuberculosis. 4-(Trifluoromethoxy)benzaldehyde can be used in assays to measure the potency of other compounds that are involved in tyrosinase activity or have anti-cancer properties. 4-(Trifluoromethoxy)benzaldehyde specifically binds to residues in the kinase domain of the enzyme tyrosinase, which is responsible for catalysis and regulation of this enzyme.</p>

<p>4-Hydroxy-3-(trifluoromethoxy)benzaldehyde is a chemical that modulates the toxicity of cells. It has been shown to reduce amyloid plaques in animals and humans with Alzheimer's disease, and to inhibit the formation of plaques in transgenic mice. In addition, 4-hydroxy-3-(trifluoromethoxy)benzaldehyde has been found to be a pyrimidine compound, which can be used as a potential treatment for alzheimer's disease. This substance also has an insoluble nature and is not soluble in water. Curcumin is one of the substances that may be used to dissolve this substance.</p>

<p>5-Fluoro-2-methylbenzaldehyde is a fine chemical that is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic molecules. It is also useful in the preparation of synthetic resins, dyes, and flavors. 5-Fluoro-2-methylbenzaldehyde has been shown to be a versatile building block with many potential applications. This molecule can be used as a reaction component or as a speciality chemical to produce high quality reagents.</p>

<p>2-Bromo-5-methoxybenzaldehyde is an organic compound that is used as a synthetic intermediate. It has been shown to be a substrate for the acid transporter SLC26A2, which transports it into cells. This compound has also been found in low levels in human tissues and fluids, where it may play a role in the development of cancer. 2-Bromo-5-methoxybenzaldehyde has been shown to inhibit the growth of cancer cells by uv absorption and terminal alkynes. The anticancer activity of this compound is due to its ability to react with functional groups such as benzyl groups and other alkyl groups.</p>

<p>2-Nitro-4-(trifluoromethyl)benzaldehyde is an immunosuppressive agent that binds to the active site of the enzyme nitric oxide synthase, inhibiting its activity. This drug has been shown to be active against human immunocompromised patients and those with a history of melamine exposure. It also inhibits the production of nitric oxide, which is associated with inflammation. 2-Nitro-4-(trifluoromethyl)benzaldehyde has been shown to bind to vinylic positions on proteins, leading to immunosuppression.</p>

<p>Chloroacetaldehyde is a reactive compound that is found in wastewater. It can be used to remove other pollutants from the water. Chloroacetaldehyde has been shown to be toxic and may cause cancer, but it also has been used as a model system for studying energy metabolism. This substance is toxic because it reacts with cellular components such as proteins and DNA by cross-linking them. The cytosolic Ca2+ concentration increases when chloroacetaldehyde binds to cellular proteins, which affects cell physiology and the production of MMP-9.</p>

<p>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.</p>

<p>5-Methoxy-2-(trifluoromethyl)benzaldehyde (5MFBA) is a potential anticancer compound that has been shown to inhibit the growth of pancreatic cancer cells. 5MFBA is formed by the reaction of methoxybenzene and trifluoromethyl bromide in the presence of copper chloride, which acts as a dehydrogenase. This compound also has prognostic and clinicopathological implications in patients with pancreatic cancer, as well as staining properties in tissues. 5MFBA modulates biological function via reactive oxygen species (ROS) production, which induces cell apoptosis. Research on this compound has been done on cancer tissues from various organs, including breast and prostate cancers.</p>

<p>2,3,4-Trihydroxybenzaldehyde is a chemical compound that has been shown to have anti-cancer properties. It is used in the detection of cancer cells and as an indicator for the presence of palladium complexes. 2,3,4-Trihydroxybenzaldehyde is also a skin allergen and can cause allergic reactions. This chemical reacts with potassium ions in solution to form a precipitate or sludge. 2,3,4-Trihydroxybenzaldehyde has been shown to be effective against colorectal carcinoma cells and Group P2 bacteria.</p>

<p>6-Benzyloxyindole-3-carboxaldehyde is a benzyl compound that is produced by the catalytic hydrogenolysis of benzyl alcohol. The debenzylation product of 6-benzyloxyindole-3-carboxaldehyde is known as benzene.</p>

<p>2,4,6-Trihydroxybenzaldehyde is a polymerase chain inhibitor that blocks the synthesis of DNA and RNA. It has been shown to have significant cytotoxicity in vitro and has been used as an antimicrobial agent to inhibit the growth of bacteria. 2,4,6-Trihydroxybenzaldehyde also inhibits tetracycline resistance in Mycobacterium tuberculosis (Mtb) by inhibiting the production of proteins vital for bacterial cell division. This compound is structurally related to naturally occurring compounds such as anthocyanins and it has been shown to have inhibitory properties on mitochondrial membrane potential, which may be due to its ability to inhibit protein synthesis and induce apoptosis. The analytical methods used for this compound are thin layer chromatography and high performance liquid chromatography.</p>

<p>3-Hydroxy-2-iodobenzaldehyde is a heterocyclic compound that is synthesized from an acetoacetic ester. It is a photochemical precursor to many organic compounds, such as phenanthrene. The synthesis of 3-hydroxy-2-iodobenzaldehyde can be achieved by reacting acetoacetic acid with iodine and sodium nitrite in the presence of a base. This reaction yields 2-iodobenzoic acid in addition to the desired product. 3-Hydroxy-2-iodobenzaldehyde has been studied for its use in the preparation of natural products and research advances.</p>

<p>4-Ethoxybenzaldehyde is a chemical compound with antioxidant properties. It has been found to inhibit the proliferation of cervical cancer cells and melanoma cells, as well as to protect against radiation-induced oxidative damage in human skin. 4-Ethoxybenzaldehyde also inhibits the influenza virus by interfering with its ability to replicate. This compound is used in many different products, including cosmetics and pharmaceuticals. The most common use of 4-ethoxybenzaldehyde is as an excipient in tablet formulations. In this application, it can be used to maintain drug stability and improve disintegration time. In addition, it may have some anti-inflammatory effects that are related to its ability to inhibit the production of prostaglandins and leukotrienes. 4-Ethoxybenzaldehyde has been shown to have antioxidant properties for diabetics as well as for patients with autoimmune diseases such as multiple sclerosis and systemic lupus erythematosus (SLE). The</p>

<p>3-Bromo-4-fluorobenzaldehyde is a drug substance that is used in the synthesis of pharmaceuticals. It is also a potential anticancer agent. 3-Bromo-4-fluorobenzaldehyde inhibits bacterial growth by binding to DNA, preventing transcription and replication. The high frequency of human activity has been shown using a patch clamp technique on human erythrocytes. This active form is metabolized through 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. 3-Bromo-4-fluorobenzaldehyde also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.</p>

<p>Phloroglucinol aldehyde triethyl ether is a high quality, research chemical, speciality chemical and versatile building block. It is used in the synthesis of complex compounds that are useful as intermediates or fine chemicals. The CAS No. for this compound is 59652-88-9.</p>

<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>

<p>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.</p>

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

<p>3,4-Dimethoxy-6-nitrobenzaldehyde is a chemical compound that has been synthesized by the reaction of 3,4-dimethoxybenzaldehyde and nitric acid. The asymmetric synthesis of 3,4-Dimethoxy-6-nitrobenzaldehyde starts with the preparation of the corresponding ester, which is then reacted with nitric acid to produce the desired product. The chemical structure of 3,4-Dimethoxy-6-nitrobenzaldehyde consists of three aromatic rings: a benzene ring fused to a phenyl ring and a pyridine ring. This chemical can be used as an intermediate in the synthesis of epidermal growth factor (EGF). It also has been shown to bind to toll like receptor 4 (TLR4), which activates NFκB signaling pathway and induces apoptosis in monocytes.</p>

<p>6-Fluoroindole-3-carboxaldehyde (6FLA) is a synthetic compound that inhibits biosynthesis of the phytoalexins salicylic acid and lignin in plants. It also inhibits the β-glucuronidase enzyme, which hydrolyzes the glucuronide conjugates of phenolic compounds and xenobiotics. 6FLA has been shown to cause mild liver damage in rats, but its effects on humans are unknown. 6FLA may be used as a detectable substance for assays.</p>

<p>3-(2-Phenylethoxy)benzaldehyde is a benzaldehyde derivative with an ether group at the 3-position. It is used as a building block for the synthesis of organic compounds and as a reaction component in the preparation of research chemicals, speciality chemicals, and complex compounds. This compound has been shown to have high purity and to be a versatile building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.</p>

<p>3-Nitrobenzaldehyde is an organic compound that is used in the synthesis of monoclonal antibodies for use in cancer research. It has been shown to have genotoxic and carcinogenic effects, as it binds to nucleic acids and inhibits DNA replication. 3-Nitrobenzaldehyde has been shown to be effective against a variety of bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. This compound also inhibits protein synthesis by binding with amines and hydrogen bonding with the amino acid residues of proteins.</p>

<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>

<p>3,4-Dihydroxy-2-nitrobenzaldehyde is a high quality chemical that is used as a reagent and as an intermediate in the synthesis of complex compounds. It has many uses, including being a useful building block for speciality chemicals, research chemicals, and reaction components. 3,4-Dihydroxy-2-nitrobenzaldehyde is versatile and can be used in the synthesis of various types of compounds. This compound is also an excellent scaffold for drug discovery.</p>

<p>4-Fluoro-2-methoxybenzaldehyde (4FMBA) is a potential PET radioligand that binds to the serotonin 5-HT2A receptor. 4FMBA has been shown to be an efficient and selective 5-HT2A antagonist with low molecular weight and high affinity. The binding of 4FMBA to the serotonin 5-HT2A receptor can be inhibited by ketanserin, which is a nonselective 5-HT2A antagonist. This drug may be used for cancer diagnosis, as it has a low detection limit and can detect endogenous serotonin in the brain. It also shows anti-depressant properties, which may be due to its ability to bind to the orthosteric site of the serotonin 5-HT2A receptor.</p>

<p>Please enquire for more information about 2-(3-Fluorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,5-Dimethyl-4-methoxybenzaldehyde is a high quality, versatile chemical that can be used as an intermediate to synthesize other fine chemicals. The compound can be reacted with various reagents to produce complex compounds. 3,5-Dimethyl-4-methoxybenzaldehyde can also be used as a building block to synthesize other useful compounds. This chemical has been shown to be a useful scaffold for the production of new compounds and has been used as a reaction component in research and development.</p>