Aldéhydes

<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-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>5-(4-Acetylphenyl)-2-furaldehyde is a fine chemical that is a versatile building block for synthesis of complex compounds. It has been used as an intermediate in the production of polyurethanes and polyesters. This compound has also been shown to be an effective reaction component in the preparation of research chemicals, such as 2,5-diacetylbenzoic acid and 4-acetamidophenol. 5-(4-Acetylphenyl)-2-furaldehyde is a high quality reagent with CAS No. 57268-39-0 that can be used in the synthesis of speciality chemicals.</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>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>5-Chloro-2-fluorobenzaldehyde is an efficient method for synthesizing substituted benzoic acid derivatives. It is a useful reagent in the acylation reaction. 5-Chloro-2-fluorobenzaldehyde also has high yields and can be used as a substitute for other more toxic or expensive compounds.</p>

<p>4-Methoxy-3-(trifluoromethyl)benzaldehyde is a fine chemical that can be used as a building block for pharmaceuticals and other organic compounds. It is also used in research for the synthesis of complex compounds. This chemical has been reported to be a useful intermediate or scaffold for organic syntheses. 4-Methoxy-3-(trifluoromethyl)benzaldehyde is soluble in water and ethanol, and insoluble in ether. It has a melting point of 140°C, boiling point of 249°C, density 1.096 g/cm³, and refractive index (20°C) 1.567.</p>

<p>Quinoxaline-5-carboxaldehyde is a versatile building block and reagent for organic chemistry. It is a complex compound that can be used as a research chemical or as a speciality chemical, with high quality and a useful scaffold. This compound has been shown to be an intermediate in the synthesis of other compounds, such as quinoxaline-5-carboxylic acid.</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>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>4-Methoxy-2-nitrobenzaldehyde is a chemical that is used in the synthesis of many pharmaceuticals. It has been shown to be an effective agent in the treatment of cancer cells and is activated by chloride ions. 4-Methoxy-2-nitrobenzaldehyde reacts with nucleophiles such as hydroxide, amines, or thiols in order to form alkylating agents. This reaction can be used for the synthesis of many drugs including antihistamines, antidiabetic drugs, and antipsychotics. The rate of this reaction increases with increasing temperature. It also undergoes demethylation when exposed to nitrous acid, which may lead to a different product.</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>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>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>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>Isoquinoline-6-carbaldehyde is a fine chemical that belongs to the group of research chemicals. It can be used as a reagent for organic synthesis, a speciality chemical, or a building block in complex organic molecules. Isoquinoline-6-carbaldehyde is also an intermediate for the synthesis of many pharmaceuticals and other useful compounds. Isoquinoline-6-carbaldehyde has been shown to react with 2-aminoethanol to form (2E)-3-(4-(1,1'-biphenyl)-2-yl)butanal, which is an important reaction component in the synthesis of nitroaromatics. Isoquinoline-6-carbaldehyde is also a versatile scaffold for the synthesis of other fine chemicals.</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>3-Bromothiophene-2-carbaldehyde is an organic compound that has been shown to have antibacterial activity. It can be synthesized by reacting triethyl orthoformate with methyl ketones in the presence of a photocatalyst such as titanium dioxide or zinc oxide. This reaction produces 3-bromothiophene-2-carboxylic acid which reacts with ammonia and hydrogen bromide to form 3-bromothiophene-2-carbaldehyde. 3-Bromothiophene-2-carbaldehyde has been shown to inhibit the growth of cancer cells and induce apoptosis, which may be due to its ability to inhibit angiogenesis. The anticancer properties are most likely due to its ability to bind DNA and inhibit protein synthesis, leading to cell death.</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>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>8-Hydroxy-5-nitroquinoline-2-carbaldehyde is a high quality, versatile building block that can be used as a reaction intermediate or to synthesize heterocycles. It is also a useful scaffold for the synthesis of complex compounds. The CAS number of this chemical is 884497-63-6.</p>

<p>6-Methoxy-1-methyl-1H-indole-3-carbaldehyde is a high quality chemical that is used as a reagent, complex compound, useful intermediate, and speciality chemical. It is a fine chemical that has been shown to be useful as a building block in the synthesis of many other compounds. 6-Methoxy-1-methyl-1H-indole-3-carbaldehyde is also versatile and can be used in reactions involving nucleophilic substitution, reductive amination, and oxidative coupling.</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>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>3,4-Difluorobenzaldehyde is a chemical inhibitor that has been shown to be effective in the treatment of cancer. It inhibits the activity of an enzyme called tyrosine kinase by reacting with its functional group, leading to decreased production of growth factors and cell proliferation. 3,4-Difluorobenzaldehyde has been shown to have a high reaction yield in animal health studies, and it can be used as a drug for treating carcinoma cells. This compound also has strong liquid crystal properties and can be used as a component of diphenyl ether molecules. 3,4-Difluorobenzaldehyde is metabolized by the liver or excreted through urine. The pharmacokinetic properties of this compound are similar to those of other drugs that are metabolized by humans.</p>

<p>2-Chloro-3,4-dimethoxy-6-nitrobenzaldehyde is a fine chemical with a CAS number of 82330-54-9. It is a versatile building block that can be used as a reagent or intermediate for the production of other chemicals. This product has been shown to have many different reactions. It is useful in the synthesis of complex compounds and offers high quality and purity.</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>2,5-Dimethoxyterephthalaldehyde (2,5DMP) is a protonated molecule that can be used in sample preparation for analytical methods. 2,5DMP has been used as a dispersive solid-phase extraction solvent and an adsorbent material. This compound has been shown to exhibit strong hydrophobic interactions with the carbonyl group of aromatic compounds and to have a high chemical stability. 2,5DMP also has an electrochemical impedance spectroscopy (EIS) property that can be used for monitoring the electrochemical behaviour of molecules and magnetic particles in the solution. The EIS property has been enhanced by hydrogen bonding between the protonated molecules and metal ions in the solution.</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>3,6-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'-Methyl-2,2'-bipyridine-4-carboxaldehyde is a heterocyclic compound that contains a nitro group. It has the chemical formula C8H6N2O and the molecular weight of 122.15 g/mol. This compound belongs to the class of formyl compounds and it is composed of two formyl groups and one hydrogen atom. The bipyridines are linked by a methylene bridge to form a six-membered ring. The compound can be used as an intermediate for the synthesis of other organic compounds such as pharmaceuticals, dyes, water repellents, pesticides, and herbicides.</p>

<p>5-Chloro-2-methoxybenzaldehyde is a potent inhibitor of the bacterial enzyme acetylcholinesterase. It has been shown to have an interaction with biomolecules, such as chalcones, and can be used in the manufacture of antibacterial agents. 5-Chloro-2-methoxybenzaldehyde has been found to have potent inhibitory activity against organocatalytic aldehydes and atypical aldehydes and can be used as an active ingredient in the synthesis of novel compounds with antibacterial activity.</p>

<p>2,5-Dibromoterephthalaldehyde is a red fluorescent compound that has been shown to have potential as a cancer therapy. The compound is able to bind to the electron acceptor 2,5-dibromoterephthalate (DBT) and can be used in photocatalytic reactions. It has been shown that 2,5-dibromoterephthalaldehyde can cause high levels of cell death in cancer cells with low levels of toxicity to healthy cells. This property may be due to its ability to target cancerous cells by binding with their mitochondria. The compound is also fluorescent and emits light when excited with UV light. 2,5-Dibromoterephthalaldehyde has been shown to form structured metallacycles in the presence of copper ions.<br>!--</p>