Aldehydes

<p>Applications 4-Pentenal acts as a reagent used in the screening of the phytochemical, antibacterial and cytotoxic activity of medicinal plant of Tamilnadu.<br>References Nameirakpam, N. D., et al.: Int. J. Pharm. Res. BioSci., 1 (2012)<br></p>

<p>Applications (2E,4E,14Z)-Octadeca-2,4,14-trienal is an intermediate of (4E,14Z)-Sphingadienine-C18 (S680630), a sphingoid base of sea cucumber cerebroside that may have cytotoxicity activity against human colon cancer cells.<br>References Liang, Z., et al.: Eur. J. Mass. Spec., 19, 195 (2013):<br></p>

<p>5-Hydroxy-4-methoxy-2-nitrobenzaldehyde is a substrate molecule that can be minimised to the corresponding oxime, which can then be oxidised to form an aldehyde. The product of this reaction is a conformationally restricted dienone. This compound has been synthesized using a number of different methods, including oxidation by sodium dichromate. 5-Hydroxy-4-methoxy-2-nitrobenzaldehyde is a phenolic compound with two aromatic rings and one carbon ring. It has natural product properties and is used as a chemical skeleton in the synthesis of other compounds.</p>

<p>1-Methyl-1H-indazole-5-carbaldehyde is a selective inhibitor of the enzyme lysine acetyltransferase (KAT). KAT inhibitors are a new class of compounds that have been shown to be effective in inhibiting the growth of acute myeloid leukaemia cells, with little effect on other cells. 1-Methyl-1H-indazole-5-carbaldehyde has potent inhibitory activity against human myeloid leukemia cells and does not affect the viability of normal human erythrocytes or peripheral blood mononuclear cells. This compound is reversible, meaning it can be turned off when it is no longer needed. 1-Methyl-1H-indazole-5-carbaldehyde has also been shown to inhibit maoA and thymidine phosphorylase in vitro.</p>

<p>3-(4-tert-Butylphenyl)isobutyraldehyde is a metal hydroxide that is synthesized by the asymmetric synthesis of 4-tert-butylbenzoic acid. The compound has been shown to be effective in increasing the mitochondrial membrane potential and preventing oxidative damage in liver cells. 3-(4-tert-Butylphenyl)isobutyraldehyde has been detected in urine samples and has been shown to be metabolized by human metabolism, with fatty acids and diphenyl ether as metabolites.</p>

<p>1,5-Dimethyl-1H-indole-3-carbaldehyde is a useful building block for organic synthesis. It is an important reagent for the synthesis of complex compounds and it has been used as a versatile building block in organic chemistry. This compound can be used as a starting point for the preparation of other chemicals, such as pharmaceuticals, pesticides, and dyes. 1,5-Dimethyl-1H-indole-3-carbaldehyde is also a fine chemical that has been used for research purposes. There are no known commercial uses for this compound.</p>

<p>3,6-Dimethoxyterephthaldicarboxaldehyde is a chemical compound that can be used in the synthesis of complex compounds. It has been shown to be an effective reagent for the synthesis of heterocycles and has also been used as a building block in the synthesis of pharmaceuticals and other organic compounds. 3,6-Dimethoxyterephthaldicarboxaldehyde is a versatile building block with many potential uses. It has also been identified as a useful scaffold for drug design and development.</p>

<p>4-Methoxy-3,5-dimethyl-2-pyridinecarboxaldehyde is a trifunctional molecule that has been shown to suppress the growth of cancer cells in mice. This compound is an inhibitor of acid synthesis and has also been shown to be an antirheumatic drug. 4-Methoxy-3,5-dimethyl-2-pyridinecarboxaldehyde inhibits the activity of three enzymes: synthetase, an enzyme that synthesizes fatty acids; 3-ketoacyl CoA synthase, which synthesizes ketones; and enoyl CoA reductase, which produces fatty acids. The long term efficacy of this molecule has not yet been studied in humans.</p>

<p>2,3-Dichlorobenzaldehyde (2,3-DBA) is an organic compound that is used as a synthetic intermediate in the preparation of other chemicals. It is prepared by reacting 2-chloroacetophenone with hydrochloric acid and sodium carbonate in a reaction vessel. The product can be purified through fractional distillation or crystallization. The optical properties of 2,3-DBA are determined by its dipole moment and the substituents attached to the methylene group. Molecular modeling studies have shown that felodipine can bind to 2,3-DBA through its active methylene group. The reaction products between sulfadiazine and 2,3-DBA are pyridinedicarboxylic acid and 3-chlorobenzaldehyde.</p>

<p>5-Fluoro-1-Methyl-1H-Indole-3-Carbaldehyde is a high quality chemical that is used as a reagent, an intermediate for the synthesis of pharmaceuticals, and in the production of fine chemicals. 5FMICA is also a useful scaffold for developing valuable building blocks. This chemical has been shown to be a versatile building block for the synthesis of complex compounds. 5FMICA can be used as a reaction component for the preparation of speciality chemicals and research chemicals.</p>

<p>1-Cyclohexene-1-carboxaldehyde (1C) is a fatty acid that is found in the blood of mammals, including humans. It can be synthesized by reacting 1-cyclohexene with t-butyl hydroperoxide and potassium t-butoxide in the presence of an acid catalyst. 1C has been shown to have antibacterial activity against Gram-positive bacteria such as Bacillus subtilis and Streptococcus pneumoniae. The oxidative products of 1C are also active against Gram-positive bacteria. These products include pyrethroid analogs, which are insecticides used for the control of insects, and alkylating agents, which are chemicals that react with DNA to form covalent bonds.</p>

<p>2-Bromo-3,6-difluorobenzaldehyde is a versatile building block that is used in the synthesis of many complex compounds. It has been shown to be a useful intermediate and reaction component in organic synthesis. 2-Bromo-3,6-difluorobenzaldehyde can be used as a reagent or speciality chemical for research purposes. This compound has high quality and is a useful scaffold for the preparation of fine chemicals.</p>

<p>4-Chloro-2-fluorobenzaldehyde is an aryl aldehyde that belongs to the class of chemical compounds known as chloroaldehydes. It can be synthesized from 4-chlorophenylacetic acid and 2,3-dichloroacetone. The compound is chiral and has two enantiomers. One enantiomer is less reactive than the other, which is more reactive. 4-Chloro-2-fluorobenzaldehyde can be used in the synthesis of a variety of organic compounds, such as pharmaceuticals, herbicides, pesticides, and dyes. This compound can also be used for microbial strain identification by liquid chromatography (LC) with ultraviolet (UV) detection. The yields are typically high (&gt;90%), and the process can be performed at room temperature without any need for vacuum or pressure conditions.</p>

<p>4-Diethylaminobenzaldehyde is an organic compound that contains a hydroxyl group. It is a fluorescent probe and can be used to measure the transcriptional regulation of genes. This molecule has been shown to be an effective fluorescence probe for the detection of cb2 receptors in Langmuir adsorption isotherms and LC-MS/MS methods. 4-Diethylaminobenzaldehyde has also been shown to have chemopreventive properties against carcinoma cells.</p>

<p>4-Phenylbenzaldehyde oxime is a high quality reagent that is used as a building block in the synthesis of complex compounds. It is an aromatic compound with a chemical formula of C8H7O2N. This product can be used to make a variety of useful intermediates, fine chemicals, and speciality chemicals. 4-Phenylbenzaldehyde oxime has been identified as a potentially useful scaffold for synthetic organic chemistry and research into new drugs. It is also used as an intermediate in the production of other organic compounds. This product has been shown to be versatile and can be used to synthesize many different types of reactions.</p>

<p>4-Isobutylbenzaldehyde is a solid phase microextraction (SPME) extractant used to remove volatile organic compounds from the air. It is an aromatic compound that has been shown to have antimicrobial activity against anthranilate-resistant strains of bacteria and fungi. SPME can be used for the extraction of polyfluoroalkyl anions, chloride, and methyl cinnamate from the environment. This extractant can also be used to cross-couple chloroformates through a palladium catalyst. 4-Isobutylbenzaldehyde is found in healthy plants as well as exudates such as those from robinia or aliphatic hydrocarbons, such as methyl anthranilate.</p>

<p>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.</p>

<p>Naphthalene 1,4-dicarboxaldehyde is a low energy focusing molecule that is used in macrocyclic compounds. It can be oxidized to form naphthalene 1,4-diacid and naphthalene 1,4-diketone. This compound has been used to synthesize the triarylmethane dye viologen by Wittig reaction. Naphthalene 1,4-dicarboxaldehyde has also been shown to have fluorescence properties and can be useful for chemiluminescence. Naphthalene 1,4-dicarboxaldehyde reacts with sulfide or amine groups to form sulfides or amines respectively.</p>

<p>2-(4-Methoxyphenoxy)benzaldehyde is a fine chemical that is used as a versatile building block in the synthesis of complex compounds and research chemicals. 2-(4-Methoxyphenoxy)benzaldehyde is also a reagent that can be used to synthesize speciality chemicals, useful building blocks, and reaction components. This chemical may be used as an intermediate for the synthesis of high-quality pharmaceuticals or other useful scaffolds. It has CAS number 19434-36-7.</p>

<p>2,3-Dimethyl-1H-indole-5-carbaldehyde is a high quality reagent that is used as a complex compound. It has been shown to be a useful intermediate and building block in the production of fine chemicals. 2,3-Dimethyl-1H-indole-5-carbaldehyde is also useful as a research chemical. This compound is versatile and can be used in reactions as an intermediate or building block. As a speciality chemical, it has various applications and is not limited to any specific area of research.</p>

<p>4-Hydroxy-3,5-dimethoxybenzaldehyde (4HMB) is a phenolic compound that can be obtained from lignin. 4HMB is the precursor in the synthesis of vanillin, which has a characteristic flavor and odor. It is also used as an additive in perfumes. The compound is found naturally in plants, such as in the bark of cinchona trees, and can be extracted using preparative high performance liquid chromatography (HPLC). 4HMB can be synthesized by reacting p-hydroxybenzoic acid with 3,4,5-trimethoxybenzyl alcohol in the presence of copper chloride. This chemical reaction results in an aldehyde form of the molecule. 4HMB binds to sodium salts to form a water soluble salt that can be used for wastewater treatment. It also has antioxidant properties due to its ability to scavenge free radicals. The enzyme activities of 4HMB are not well</p>

<p>2-Ethylbenzaldehyde is a colorless volatile liquid that has an odor similar to that of cloves. 2-Ethylbenzaldehyde can be found in the essential oil of nutmeg and other spices, such as cinnamon. It is used in the chemical industry as a control agent for analytical methods, such as the spectrometric determination of ether linkages. 2-Ethylbenzaldehyde has been shown to inhibit fatty acid production by bacteria and to inhibit lipid peroxidation. It also exhibits anti-inflammatory effects when exposed to cells in vitro. Exposure to 2-ethylbenzaldehyde may cause irritation of the eyes, skin, and respiratory tract, dizziness, headache, nausea and vomiting.<br>2-Ethylbenzaldehyde is generally considered safe for human consumption at low levels; however it may cause adverse health effects if ingested in large quantities or if heated over 400° F (204° Celsius).</p>

<p>2-Bromo-5-fluorobenzaldehyde is a chemical compound that has been shown to inhibit the activity of ns3 protease, an enzyme responsible for the cleavage of peptides in HIV. 2-Bromo-5-fluorobenzaldehyde binds to the active site of ns3 protease and prevents it from carrying out its function. This drug has also been shown to bind to the active site of ns5b polymerase and inhibit its activity, which is necessary for viral DNA synthesis. 2-Bromo-5-fluorobenzaldehyde has been used as a fungicide and has shown high potency against Candida albicans, Cryptococcus neoformans, Saccharomyces cerevisiae, and Aspergillus fumigatus.</p>

<p>Benzo[d]oxazole-5-carbaldehyde is a chemical compound that can be used as a building block in the synthesis of more complex molecules. It is a high quality, versatile building block with many applications. Benzo[d]oxazole-5-carbaldehyde can be used as a reagent in organic chemistry and as a reaction component in the synthesis of more complex compounds. This compound can also serve as an intermediate or scaffold for the synthesis of other compounds.</p>

<p>3,5-Dibromo-4-hydroxybenzaldehyde is an aldehyde that is used as a precursor to other organic compounds. It can be produced using the efficient method of reacting 3,5-dibromo-4-hydroxybenzoic acid with sodium borohydride in methanol. The molecule has three hydroxymethyl groups and two functional groups. 3,5-Dibromo-4-hydroxybenzaldehyde is soluble in water and organic solvents such as ethanol and acetone. This compound has shown antibacterial activity against some strains of bacteria, including group P2 bacteria. The reaction yield for the synthesis of this compound is approximately 93%. The inhibitory activities of 3,5-dibromo-4-hydroxybenzaldehyde have been demonstrated against both Gram positive and Gram negative bacteria.</p>

<p>2,6-Dimethylbenzaldehyde is a colorless liquid with a sweet odor. It is used in the synthesis of fatty acids and as an intermediate for other compounds. This chemical has significant cytotoxicity against leukemia cells, and is used in the production of acrylonitrile. 2,6-Dimethylbenzaldehyde can be synthesized by reacting an amine with an acyl chloride, followed by hydrolysis of the resulting ester. A contactor is usually added to facilitate the reaction. The reaction can also be carried out in the presence of a phosphorane or organic solvent.<br>2,6-Dimethylbenzaldehyde can be hydrogenated to produce 2,4-dimethylaniline and 2,4,6-trimethylaniline.</p>

<p>3-Methoxy-4-(difluoromethoxy)benzaldehyde is a chemical compound that has been found to have anti-tumor properties. It inhibits tumor cells by inducing cell apoptosis. 3-Methoxy-4-(difluoromethoxy)benzaldehyde induces apoptosis in human carcinoma cells, with optimal activity at doses of 10 micromolar and higher. This chemical can be used as an anti-tumor agent because it shows no genotoxic effects, and has high yield with a low toxicity profile. When this compound is exposed to UV radiation, the formation of reactive oxygen species (ROS) increases the rate of cell death. 3-Methoxy-4-(difluoromethoxy)benzaldehyde also has anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>(E)-2-Hexadecenal is an asymmetric molecule that is a reactive and carcinogenic compound. It has been shown to induce c-Jun phosphorylation in the human carcinoma cell lines, leading to physiological changes. (E)-2-Hexadecenal has also been used to induce chemiluminescence in vitro, which can be used for analytical chemistry. It is made by a hydroxyl group on a fatty acid with a biofuel reaction. This molecule may also have pro-apoptotic properties due to its chemical biology and ability to affect mitochondrial membrane potentials.</p>

<p>4-Chloro-1H-pyrazole-3-carboxaldehyde is a fine chemical that is used as a building block in research and development. The CAS number is 623570-54-7. This compound has been found to be useful in the synthesis of complex compounds and versatile scaffolds.</p>

<p>Betulinaldehyde is a natural compound that belongs to the group of betulinic acid. It has been shown to have antimicrobial activity against oral pathogens and has been shown to inhibit the growth of bacteria by reacting with their cell walls. Betulinaldehyde has also been shown to have an effect on autoimmune diseases such as multiple sclerosis, as well as infectious diseases such as HIV and tuberculosis. Betulinaldehyde can be extracted from the bark of birch trees using acetate, which is then reacted with hydrogen peroxide in a reaction solution. The resulting product is purified using preparative high-performance liquid chromatography (HPLC).</p>

<p>6-Hydroxy-2-naphthaldehyde is a reactive compound that is used to measure the fluorescence resonance of mitochondria. It is a fluorophore that has been used as a probe for the measurement of membrane permeability, and as a hydroxyl group it can be converted into 6-hydroxy-2-naphthalenecarboxylic acid which is used in the production of dyes. 6-Hydroxy-2-naphthaldehyde has been shown to have congestive heart effects in mice, but this effect may be due to its ability to induce naphthalene and formamide.</p>

<p>2,6-Dibromobenzaldehyde is an imidazole derivative that has been shown to be a potent inhibitor of tyrosine kinase. It has been shown to inhibit the replication of virus type-1 and is effective in the treatment of pain models. 2,6-Dibromobenzaldehyde also inhibits the activity of enzymes, such as phosphodiesterases and protein kinases. This compound has shown promising results in animal studies for the treatment of human immunodeficiency virus type 1 (HIV-1) infection. The pharmacokinetic properties of 2,6-dibromobenzaldehyde have been studied in rats and dogs with oral administration and found to be linear and rapid with high bioavailability.</p>

<p>3-Ethynylbenzaldehyde is a tryptic, nitro compound that contains terminal alkynes and has functional groups. The functional theory of this compound suggests that it may be used as a chemosensor for the detection of acidic compounds. 3-Ethynylbenzaldehyde reacts with sodium trifluoroacetate to form an aldehyde, which is then oxidized to an acid by the addition of water. This acid can be detected using NMR spectroscopy. 3-Ethynylbenzaldehyde has been shown to react with sodium trifluoroacetate in solid form at room temperature and above. The resulting product is a yellow crystalline solid that can be identified by its UV spectrum.</p>

<p>5-Chloro-2-(trifluoromethyl)benzaldehyde is a fine chemical that can be used as a versatile building block for organic synthesis. It has CAS number 90381-07-0 and is an intermediate in the synthesis of a variety of organic compounds. 5-Chloro-2-(trifluoromethyl)benzaldehyde is also an effective reagent for the preparation of complex compounds. It is soluble in polar solvents, such as chloroform, ethanol, ether, acetone, and benzene.</p>

<p>5-Bromo thiophene-2-aldehyde is a trifluoroacetic acid derivative used as an activatable probe for the study of biomolecular interactions. This compound has been shown to be biocompatible and has a low cytotoxicity. 5-Bromo thiophene-2-aldehyde binds to malonic acid in the presence of x-ray radiation and forms a complex that can be detected by electrochemical impedance spectroscopy. The structure of this complex was determined by x-ray crystal structures. This probe is also able to bind to nitrogen atoms in proteins, which can be used to diagnose cancer resistance through protease activity. 5-Bromo thiophene-2-aldehyde is isolated as its hydrochloride salt, which can be purified with a suzuki coupling reaction.</p>

<p>Intermediate in the synthesis of ipragliflozin</p>

<p>3-Allyl salicylaldehyde is a fluorescent probe that is used to measure the mitochondrial membrane potential. It can be used as an amine-reactive fluorescence probe for the detection of amines such as histamine and serotonin. 3-Allyl salicylaldehyde has been shown to bind to metal complexes, such as palladium complexes, immobilized on silica gel. The cavity of the immobilized metal complex acts as an adsorption site for 3-allyl salicylaldehyde, which binds to the cavity by means of a metal chelate mechanism. This binding results in an alteration in the absorption spectra and x-ray absorption properties of 3-allyl salicylaldehyde. The hydroxyl group of 3-allyl salicylaldehyde is not involved in this binding process with the immobilized metal complex, while its carbonyl group is important for this interaction.</p>

<p>3,4,5-Trifluorobenzaldehyde is an aldehyde that can be synthesized in the laboratory. It reacts with ammonium nitrate and fatty alcohols to form 3,4,5-trifluoro-1-(alkyloxy)benzene. This reaction proceeds via a dipole mechanism and produces an intermediate called 2-amino-2-nitroethanol. This intermediate then undergoes dehydrogenation to produce 3,4,5-trifluoroethanol and ammonia. The reaction time for this process varies depending on the immobilization of the reactants and the temperature of the reaction.</p>