Aldéhydes

2,5-Dihydroxybenzaldehyde is a compound that can be used as an antioxidant. It is also a precursor for the synthesis of benzalkonium chloride. 2,5-Dihydroxybenzaldehyde reacts with p-hydroxybenzoic acid to form 2,5-dihydroxyphenylacetic acid and benzoic acid. The reaction mechanism of 2,5-dihydroxybenzaldehyde has been studied in detail using hl-60 cells and has been shown to be significant cytotoxicity. The hydroxyl group in this molecule creates a hydrogen bond with the carbonyl group in p-hydroxybenzoic acid and the two react together to form products. This reaction is catalyzed by Michaelis–Menten kinetics and proceeds via an electrochemical detector. Nitrogen atoms are not present in this molecule but do exist in benzalkonium chloride, which is synthesized from 2

5-Bromoindole-3-carboxaldehyde is a water molecule that has been crystallized in the form of an amide. It is a chemical substance with asymmetric synthesis and significant antifungal activity. 5-Bromoindole-3-carboxaldehyde is active against some strains of the fungus Candida albicans and has been shown to inhibit the growth of kidney cells. This molecule also binds to the neurokinin 1 receptor and is used as a probe for fluorescence studies. The efficient method for synthesizing 5-Bromoindole-3-carboxaldehyde includes using silico analysis to confirm the structure on a computer, then performing an asymmetric synthesis with an acid catalyst to produce this compound.

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.

2-Chloro-6-fluorobenzaldehyde oxime is the chemical compound with the formula ClCH=C(O)N(OH)Cl. It is a white solid that is soluble in water and ethanol. 2-Chloro-6-fluorobenzaldehyde oxime is used as a versatile building block in organic synthesis, for example as a reagent for the preparation of amides, esters, and nitriles. It is also useful as a reagent for the conversion of ketones to nitriles.

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.

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.