Aldehydes

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3-Chloro-4-methylbenzaldehyde is an aldehyde that reacts with hypochlorite to form chloral hydrate. It is used as a reagent for the chlorination of aliphatic and aromatic aldehydes. 3-Chloro-4-methylbenzaldehyde has been shown to be efficient in the formation of chloral hydrate, which can be used in the synthesis of organic compounds. The electron donating groups on this molecule are responsible for its reactivity with hypochlorite.

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2,6-Dimethyl-4-hydroxybenzaldehyde is a synthetic compound that belongs to the class of aminoguanidines. It has been shown to be a potent vasoprotective agent and is used in the treatment of cardiovascular diseases. 2,6-Dimethyl-4-hydroxybenzaldehyde reverses the effects of formate on the jejunum by inhibiting secretion and intestinal motility. The activity of this drug has been shown to be due to its inhibitory effect on histamine release from mast cells.

2-(Ethylthio)pyrimidine-5-carbaldehyde is a thioether that is soluble in organic solvents. It can be synthesized using the electrochemical properties of the substituents on the gold electrode. 2-(Ethylthio)pyrimidine-5-carbaldehyde has been shown to inhibit anionic polymerization and anionic electropolymerization, which are important for chemical reactions that form polymers or plastics. This compound has also been shown to be able to form fullerenes, which are spherical carbon molecules composed entirely of hexagons and pentagons. The discovery of this compound could lead to advances in chemical synthesis.

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3-Bromo-5-chlorobenzaldehyde is a fine chemical that is used as a building block in the synthesis of other chemicals. It is also a reagent and speciality chemical with high quality and versatility. 3-Bromo-5-chlorobenzaldehyde has been shown to be useful in the preparation of complex compounds, such as heterocyclic aromatic compounds, which are versatile scaffolds for drug discovery. 3-Bromo-5-chlorobenzaldehyde has a CAS No. 188813-05-0.

Thiophene-3-carboxaldehyde is an electron-rich, reactive chemical substance that can be used as a polymer film. It is a heterocyclic compound with a thiophene ring and a carbonyl group in the 3-position. Thiophene-3-carboxaldehyde is synthesized by reacting methyl ketones with glycol ethers. This reaction produces redox potential, malonic acid, and nmr spectra.

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

2-Fluoropyridine-3-carboxaldehyde (FP) is an antibiotic that has been synthesized and tested in vitro against a range of bacterial strains, with promising results. FP has shown activity against Gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Streptococcus pneumoniae. FP also inhibits the growth of Gram-negative bacteria such as Escherichia coli and Klebsiella pneumoniae. The compound has been shown to be active against some fungi and yeast strains, but not against viruses or other microorganisms. FP can be used in conjugates with anticancer drugs to target tumor cells that are resistant to chemotherapy.

2-Thiophenecarboxaldehyde is a synthetic compound that has been shown to have in vitro antifungal activity. It has also been shown to inhibit the growth of bacteria and fungi, such as Candida albicans. The antimicrobial activity of 2-thiophenecarboxaldehyde has been demonstrated by in vitro studies using human serum, metal carbonyl complexes, and sodium salts. In addition, this compound inhibits the synthesis of proteins in animal cells infected with viruses or bacteria. It also has amoebicidal activity against Entamoeba histolytica and Leishmania donovani. This compound is used for the treatment of autoimmune diseases such as rheumatoid arthritis and multiple sclerosis.

Cyclopropaneacetaldehyde is a reactive hydroxy group-containing compound. It is an organic ester that can be used as an antimicrobial agent. Cyclopropaneacetaldehyde has been shown to have pesticidal activity against insects, mites, and other arthropods, although it is not active against nematodes. This ester is also a precursor for the synthesis of heterocycles by oxidation with a transition metal catalyst. Cyclopropaneacetaldehyde has been found to be highly toxic to cancer cells in vitro.

1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde is a molecule that inhibits the activity of the protein tyrosine kinase, which is involved in the regulation of cell growth. It has demonstrated potential as an anticancer agent and has shown anticancer activity against cancer cells resistant to other treatments. Preliminary studies have been conducted with this compound, but more research is needed before it can be used in clinical trials. The safety profile of 1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde has not been established.

BR1235 - 4-Hydroxybenzaldehyde

2-Hydroxy-1,3,5-benzenetricarbaldehyde is a molecule with hydrophilic properties. It contains two aldehyde groups and is an electron deficient molecule. 2-Hydoxy-1,3,5-benzenetricarbaldehyde has been shown to have photocatalytic activity. This compound can be used to introduce anions into organic molecules. 2-Hydroxy-1,3,5-benzenetricarbaldehyde has also been shown to react nucleophilically with indolium salts and form chemical structures that are related to functional theory. Fluorescence probes are commonly used in the study of 2-hydroxybenzaldehyde because it has a high fluorescence quantum yield.

1-Oxo-1,2,3,4-tetrahydronaphthalene-2-carbaldehyde is a chiral compound with the chemical structure of an organic cyclic compound. It has a 6 membered heterocyclic ring. This substance is also known as pyrollo and is used in organic chemistry for the synthesis of squaramide analogs. 1-Oxo-1,2,3,4-tetrahydronaphthalene-2-carbaldehyde can be prepared through an organocatalytic reaction using oleum as the catalyst and benzyl bromide or benzyl chloride as the starting material. The yields are high when pyridyl methides are used as a substructure. The chromophore in this molecule absorbs light at 430 nm.

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Phenylpropargylaldehyde is an organic compound that is a chiral molecule, which means it has two enantiomers. It was first synthesized in 1964 by R.B. Woodward and T.W. Rittenberg at the University of Chicago, and is used as a chemical intermediate in the synthesis of other compounds with biological activity such as matrix metalloproteinase inhibitors, for example marimastat. Phenylpropargylaldehyde can be prepared from malonic acid and phenylboronic acid in a reaction mechanism that involves nucleophilic substitutions, carbonyl group activation and hydrogen bonding to lysine residues on proteins. The asymmetric synthesis of this compound has been shown to suppress genes associated with metabolic disorders such as diabetes mellitus type 2, fatty acid metabolism disorders and endocrine disorders (e.g., thyroid). It also has adjuvant therapeutic properties in cancer treatment, especially when combined with synthetic fatty acids such as oleic acid or ar

3-Fluoropyridine-2-carbaldehyde is a compound that can be synthesized by reacting 3-fluoropyridine with formaldehyde. The synthesis of this molecule is an example of synthetic chemistry, which is the process of creating new molecules from simple starting materials. 3-Fluoropyridine-2-carbaldehyde has been shown to have anticancer activity in vitro. This compound has also been shown to have physicochemical properties that make it a potential candidate for drug development. The molecule contains a benzoylhydrazone group, which can bind metal ions and water molecules. In addition, this molecule contains an enolate group, which can bind to other organic molecules when it is protonated.

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.

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