Aldéhydes

2-Chloro-5-hydroxybenzaldehyde is an organic compound that can be used as a starting material for the synthesis of many other chemicals. It is a building block for the production of high quality and fine chemicals, such as research chemicals and speciality chemicals. 2-Chloro-5-hydroxybenzaldehyde also has versatile uses in chemical reactions, such as condensation reactions, nucleophilic substitution reactions, and electrophilic addition reactions. The CAS number of this chemical is 7310-94-3.

4-(4-Ethylphenyl)benzaldehyde is a high quality, reagent, complex compound. CAS No. 101002-44-2. It is a useful intermediate and fine chemical that can be used as a versatile building block for the synthesis of speciality chemicals such as research chemicals and reaction components. This chemical is an excellent starting material for the synthesis of useful scaffolds and useful building blocks.

3-Nitrosalicylaldehyde is an oxidizing agent that reacts with DNA in vitro to form DNA adducts. 3-Nitrosalicylaldehyde also has antioxidative properties, which can be demonstrated by its ability to inhibit the oxidation of low density lipoprotein (LDL) in vivo. This compound has been shown to activate the metalloproteinase MT2 receptor, which is involved in the regulation of blood pressure and heart function. 3-Nitrosalicylaldehyde is metabolized by hydrolysis and reduction to form a neutral product, which has been shown to have antidiabetic effects on mice.

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.

1,10-Phenanthroline-2-carbaldehyde is a phenylhydrazone compound that has been shown to have anticancer activity. It is also a supramolecular complex, which means it can form hydrogen bonds and coordinate bonds with other molecules. The anticancer activity of 1,10-phenanthroline-2-carbaldehyde may be due to its ability to inhibit the growth of prostate carcinoma cells. This compound also inhibits the growth of human cervical carcinoma cells by binding to their DNA and inhibiting the synthesis of RNA and protein. 1,10-Phenanthroline-2-carbaldehyde is being studied for its potential as an inhibitor of tumor angiogenesis.
1,10-Phenanthroline-2-carbaldehyde has been shown to have antiplatelet aggregation effects in platelets from healthy humans as well as those with type 2 diabetes mellitus or chronic kidney disease.

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.

5-Carboxyvanillin is the oxidation product of isoeugenol and p-hydroxybenzoic acid. It can be produced by reacting these two compounds with a peroxide in an oxidizing reaction. The reaction products include 5-carboxyvanillic acid, which can be hydrolyzed to vanillin. 5-Carboxyvanillin is a white crystalline solid with a chemical nature similar to that of vanillin. It has been shown to have antimicrobial properties against tissues, such as guinea pig ileum and rat liver, but not against bacterial cultures. This compound may also be used in pulping processes for the production of paper or cellulose fibers.

2-Phenylindole-3-carboxaldehyde is an organic compound that belongs to the class of bioactive molecules. It is a nitrogen heterocycle that has been shown to inhibit the growth of cancer cells in culture. 2-Phenylindole-3-carboxaldehyde has also been shown to have anti-inflammatory and antimicrobial properties. This molecule can be used in the treatment of cancer, as it inhibits the growth of tumor cells by inhibiting DNA synthesis, which leads to cell death. The molecular structure can be altered by allylation or replacement with other functional groups. The 2-phenylindole moiety can be modified at its C2 position, altering its pharmacological properties and may lead to new anticancer drugs.

5-Iodo-2,3-dimethoxybenzaldehyde is a fine chemical that is useful as a scaffold for the synthesis of other compounds. It can be used as an intermediate for research chemicals or as a reaction component in the synthesis of complex compounds. 5-Iodo-2,3-dimethoxybenzaldehyde is used for the manufacture of high quality reagents and building blocks.

3-Fluoro-4-methoxybenzaldehyde is a chemical compound that is used in the synthesis of natural products. It has been shown to have inhibitory properties against cancer cells, and has been synthesized as an analog of 3-fluoro-4-hydroxybenzaldehyde. The biological function of 3-fluoro-4-methoxybenzaldehyde is not yet known. Hydrochloric acid may be used to react with 3-fluoro-4-methoxybenzaldehyde to form a salt. This chemical also has anti-tumor effects and can be synthesized using cryogenic techniques.

4-(Bromomethyl)benzaldehyde is a chemical compound that can be synthesized by the reaction of benzaldehyde with bromine in the presence of a base. This compound has been shown to bind to human immunoglobulin G, formyl group and photophysical properties. 4-(Bromomethyl)benzaldehyde has also been used as a model for cancer studies because it binds to DNA and forms an imine bond with thymine. It has been used as a reagent for analytical methods such as phosphotungstic acid, which is a reagent used to detect proteins. The mechanism of this compound is not yet fully understood, but it may involve the formation of an imine bond with thymine in DNA.

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5-(4-Chlorophenyl)-2-furaldehyde (5-CPFA) is an antitubercular drug that inhibits the growth of tuberculosis bacteria by disrupting the synthesis of DNA. It is a functional theory that 5-CPFA inhibits the bacterial enzyme, chalcone hydroxylase, which is involved in the conversion of chalcones to flavones. This inhibition prevents the formation of reactive oxygen species and leads to cell death. The mechanism of action for 5-CPFA has been shown to be due to its ability to form covalent bonds with metal ions such as copper, zinc, and iron. When exposed to ultraviolet radiation, this compound reacts with these metal ions and causes bond cleavage in DNA strands. The resulting damage in DNA strands leads to cell death within hours.

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2,3-Dimethoxybenzaldehyde is a chemical substance that binds to its ligands by hydrogen bonding and van der Waals forces. It is used in the synthesis of diethyl succinate. 2,3-Dimethoxybenzaldehyde has been shown to inhibit the growth of squamous carcinoma cells. The conversion of 2,3-dimethoxybenzaldehyde into benzoquinone is catalyzed by glucose oxidase and peroxidase. This oxidation process results in a loss of two electrons and one proton from the molecule, changing it from a phenol to an aromatic hydrocarbon.

4-Chloropyridine-3-carboxaldehyde (4CPCA) is a potent inhibitor of the enzyme, formylation. 4CPCA is synthesized in an experimental method involving reaction of 4-chloropyridine and 3-bromoformaldehyde with a base, followed by hydrolysis to produce the desired product. This compound has been shown to inhibit formylation in vitro with inhibition potentials as high as 5000 μM. The IC 50 value for 4CPCA was found to be 0.6 mM. Formylation activity was inhibited in cell free systems and in cells from rat liver and human erythrocytes. The pharmacokinetic profile of 4CPCA is dose dependent and it is metabolized into inactive compounds by oxidation or conjugation with glucuronic acid.

1-Acetyl-3-indolecarboxaldehyde is a ligand that binds to the cannabinoid receptor 1 (CB1). It has been shown to bind to the CB1 receptor with high affinity and selectivity. In addition, it has been demonstrated to inhibit the proliferation of human breast cancer cells in vitro. The compound is used as a fluorescent probe for cb1 receptor binding. Data obtained from molecular modelling studies have suggested that the hydroxyl group might be involved in binding to the CB1 receptor. 1-Acetyl-3-indolecarboxaldehyde also binds carotenoids, which are molecules responsible for giving plants and other photosynthetic organisms their coloration. This compound can be found in many different plants, such as carrots and bananas, where it acts as an antioxidant.

Prenalterol is a drug that can be used to treat congestive heart failure and high blood pressure. It belongs to the class of 2-adrenergic receptor agonists, which are drugs that stimulate the sympathetic nervous system. Prenalterol has been shown to have a positive effect on the cardiovascular system by increasing cardiac output. This drug also has an anti-inflammatory effect, which may be due to its ability to inhibit protein synthesis genes in cells. Prenalterol has also been shown to reduce post-myocardial infarction remodeling by reducing myocardial fibrosis, although it does not affect the incidence of myocardial infarcts.

2,4-Dimethylbenzaldehyde is used in the diagnosis of cancer. It reacts with acetaldehyde to form a compound that binds to hemoglobin and is excreted in the urine, leading to a diagnostic test for cancer. 2,4-Dimethylbenzaldehyde has been shown to be genotoxic in both in vitro and in vivo studies. This aromatic hydrocarbon has been shown to cause DNA strand breaks in the target cells through a reaction mechanism involving radical formation from acetaldehyde. In addition, 2,4-Dimethylbenzaldehyde has been shown to have genotoxic effects on mice exposed by inhalation or injection.

4-Methoxybenzaldehyde is a surfactant with a Langmuir adsorption isotherm. It can be used in analytical methods for the determination of sodium carbonate at concentrations of 1 mg/mL and higher. The redox potentials of 4-methoxybenzaldehyde are +0.37 and -0.35 volts, which corresponds to group P2. The reaction mechanism for 4-methoxybenzaldehyde is the oxidation of the compound by potassium permanganate (KMnO4) in aqueous solution to form 4-hydroxybenzoic acid (4HB). The fluorescent derivative of 4-methoxybenzaldehyde is magnesium salt, which has been shown to react with ryanodine receptors in skeletal muscle cells, leading to a decrease in calcium release from the sarcoplasmic reticulum. Process optimization may be necessary for this product due to its limited applications in analytical chemistry.

2-Oxocyclohexanecarbaldehyde is a bifunctional carbonyl compound that reacts with amines to form carbinols. It can be used as a cheaper and more environmentally friendly alternative to the use of piperidine. 2-Oxocyclohexanecarbaldehyde also reacts with potassium hydride to form the corresponding ketones. The reaction of 2-oxocyclohexanecarbaldehyde with primary amines leads to isomeric products, depending on the position of substitution on the aromatic ring. This compound has been shown to react electrochemically in an asymmetric synthesis and has been used in the synthesis of morpholine, which is an important intermediate for pharmaceuticals, agrochemicals, and other chemical compounds.

Trifluoroacetaldehyde is a chemical with aqueous solubility of 0.2 g/L at 25 °C. It has been used in the preparation of insoluble polymers, such as phosphonates and polyurethanes. Trifluoroacetaldehyde can be prepared by reacting anhydrous hydrogen fluoride with trifluoroacetic acid in the presence of amines and an oxidizing agent, such as phosphorus pentoxide. The reaction mechanism is believed to involve a cationic polymerization involving hydrolysis of the amine to give an ammonium ion that reacts with hydrogen fluoride to form trifluoroacetyl fluoride and ammonium chloride. Trifluoroacetaldehyde has also been used in asymmetric synthesis, hydroxyl group reactions, pharmaceutical preparations, and monoclonal antibody production.

1H-Pyrrole-2-carbaldehyde is a compound that belongs to the class of ferrocenecarboxylic acids. It is a coordination complex with a pyrrole system and an intramolecular hydrogen bond. The proton on the carbonyl carbon atom forms hydrogen bonds with nitrogen atoms, which are located in the immediate vicinity of the carbonyl group. The structure was determined by x-ray diffraction studies and the reactivity was studied by means of X-ray crystal structures. This compound has been used for biological studies as well as for structural analysis.

2-Benzyloxy-3-methoxybenzaldehyde is an enantiopure compound that has been shown to have antiproliferative effects on cancer cells. It was also found to have a strong binding affinity for DNA and protein. The antiproliferative effects of 2-Benzyloxy-3-methoxybenzaldehyde were found to be due to its ability to bind to dna and inhibit the enzyme activity of pyrazine-2-carboxylic acid, leading to a decrease in the production of proteins vital for cell division. 2-Benzyloxy-3-methoxybenzaldehyde has been shown to have anticancer activity against colorectal cancer cells and may serve as a lead compound for future drug development.

2,3-Dihydroxybenzaldehyde is a chemical compound that has been shown to have antimicrobial properties. It inhibits bacterial growth by binding to the ribosome and preventing mRNA synthesis. 2,3-Dihydroxybenzaldehyde binds to the 50S ribosomal subunit and prevents protein synthesis by inhibiting the transfer mechanism of tRNA from the A site to the P site on the ribosome. The drug also inhibits mitochondrial superoxide production in V79 cells and human serum.
2,3-Dihydroxybenzaldehyde has been shown to be effective against methicillin resistant S. aureus (MRSA) strains but not against Group P2 Staphylococcus aureus (GPA). It is also active against Gram-positive bacteria such as Bacillus subtilis but not against Gram-negative bacteria like Escherichia coli or Pseudomonas aeruginosa.

1-Naphthaldehyde is a coordination compound that contains 1 naphthyl group and an oxygen atom. It can be used as an oxidation catalyst, intramolecular hydrogen, or a reaction solution. The antimicrobial activity of 1-naphthaldehyde has been shown in the presence of sodium carbonate or potassium phosphate buffer. 1-Naphthaldehyde has been shown to possess structural properties similar to those of other metal chelates, such as zinc pyrithione. The protonated form of 1-naphthaldehyde has been identified by means of analytical methods including gas chromatography and mass spectrometry.

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3-Phenoxybenzaldehyde is a chemical compound that is used as an analytical reagent in the surface methodology. It can be synthesized from 3-phenoxybenzoic acid and phenylmagnesium bromide. The synthesis of 3-phenoxybenzaldehyde was accomplished by the hydrogenation of p-nitrophenyl phosphate, which was catalyzed by rat liver microsomes. The resulting product had a molecular formula of C9H8O2 and a molar mass of 156.2 g/mol. 3-Phenoxybenzaldehyde has been shown to inhibit bacterial growth through the inhibition of fatty acid synthesis, as well as inhibiting fatty acid oxidation in recombinant cytochrome P450 enzymes.

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2,4,5-Trimethylbenzaldehyde is a cell line that can be used to study the oxidation of α-pinene. It is a chemical compound that belongs to the group of aromatic compounds and has been shown to have high cytotoxicity. It has been found to oxidize other molecules in the body with an electron acceptor such as oxygen or another molecule. 2,4,5-Trimethylbenzaldehyde has also been shown to have biological properties. This product is being researched for its ability to inhibit fatty acid synthesis and reduce cholesterol production in the liver.

Echinatin is a benzaldehyde derivative that is found in the roots of Echinacea purpurea. It is a phenolic compound with a carbonyl group and two benzyl groups. 4-Hydroxy-2-methoxybenzaldehyde has been shown to have photophysical, cell culture, and functional group properties. This compound is used as a precursor for the production of echinatin and other plant polyphenols such as malonic acid. The biosynthesis of 4-hydroxy-2-methoxybenzaldehyde begins with the oxidation of cinnamic acid by cytochrome P450 monooxygenase to form cinnamoyl CoA. The enzyme cinnamate decarboxylase then converts this intermediate to p-hydroxybenzoic acid, which is then hydroxylated to form 4-hydroxy-2-methoxybenzaldehyde.

4-Benzyloxy-3,5-dimethylbenzaldehyde is a potent anticancer drug that inhibits cell proliferation and induces apoptosis. It has been shown to inhibit the growth of prostate cancer cells and human erythroleukemia cells. This compound also has antibacterial activity against gram-positive bacteria such as methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium tuberculosis. 4-Benzyloxy-3,5-dimethylbenzaldehyde binds to the flavone binding site on the enzyme DNA gyrase and topoisomerase IV in both bacterial and mammalian cells. This binding leads to inhibition of DNA synthesis by preventing the formation of an enzyme complex with DNA polymerase. A study has shown that apigenin, one of the flavone derivatives found in this compound, enhances the antitumor activity of cisplatin by inhibiting DNA repair mechanisms in human cancer cells.