Aldeídos

<p>2,4,5-Trimethoxybenzaldehyde is a natural compound that belongs to the group of sephadex g-100. It is used as an absorbent and has been shown to react with human immunoglobulin in the presence of tiglic acid. The reaction mechanism for this chemical is not well understood but it is believed that intermolecular hydrogen bonding may be occurring. 2,4,5-Trimethoxybenzaldehyde has been shown to have anti-inflammatory effects when tested on rats in a laboratory setting. This chemical has also been used as an analytical reagent for biological samples and biological studies as well as a preparative hplc column. Optical sensors have also been used to detect this chemical in various types of optical sensing experiments. X-ray crystal structures have also been obtained for this compound using synchrotron radiation.</p>

<p>4-Hydroxy-3-nitrobenzaldehyde (4NBA) is a chemical compound that belongs to the class of aromatic compounds. It is an intermediate in the synthesis of various pharmaceuticals, including benzocaine and nitroglycerin, and has been researched for its potential use in cancer diagnosis. 4NBA has shown optical properties that allow it to be used as a model system for studying the interactions between water and benzyl groups. It also possesses anti-inflammatory properties due to its ability to inhibit the production of inflammatory cytokines such as IL-1β, IL-6, and TNFα.</p>

<p>4-(Trifluoromethoxy)benzaldehyde is a chemical compound that is a substrate for tyrosinase and an inhibitor of the enzyme. It is also an anticancer compound that can be used to inhibit tumor growth by inhibiting protein synthesis. 4-(Trifluoromethoxy)benzaldehyde has been shown to have potent tyrosinase inhibition activity in vitro and in vivo, as well as binding activities with the CB2 receptor. This chemical has also been shown to inhibit virus replication, including HIV-1, and tuberculosis. 4-(Trifluoromethoxy)benzaldehyde can be used in assays to measure the potency of other compounds that are involved in tyrosinase activity or have anti-cancer properties. 4-(Trifluoromethoxy)benzaldehyde specifically binds to residues in the kinase domain of the enzyme tyrosinase, which is responsible for catalysis and regulation of this enzyme.</p>

<p>3-Bromo-5-chloro-2-hydroxybenzaldehyde is a molecule that contains nitrogen atoms. It has coordination geometry and a chelate ring. 3-Bromo-5-chloro-2-hydroxybenzaldehyde also has electrochemical properties, which can be studied by cyclic voltammetry. This molecule is a copper complex that exhibits fluorescence properties and dihedral angles. The magnetic resonance spectrum of 3-bromo-5-chloro-2 hydroxybenzaldehyde displays hydrogen bonding interactions and an imine nitrogen. 3BChBrOH also absorbs light at wavelengths of 280 nm (max) and 240 nm (min).</p>

<p>2-Hydroxy-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]benzaldehyde is a reaction component that is used in the synthesis of organic compounds. It has been shown to be an effective reagent and can be used in the synthesis of high quality compounds. CAS No. 308085-25-8, it is a research chemical that can be used as a useful scaffold or building block for other compounds. 2-Hydroxy-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]benzaldehyde may also be useful as an intermediate or building block in complex synthesis reactions.</p>

<p>5-Methylindole-3-carboxaldehyde (5MI) is a β-unsaturated aldehydes that is used as an analyte in assays for the detection of α,β-unsaturated aldehydes. It has been shown to be effective in degranulation of cells and induces cellular degranulation. 5MI has also been shown to be an analog of other β-unsaturated aldehydes and acts competitively with these compounds.</p>

2-Carboxy-3,4-dimethoxybenzaldehyde is a chemical that belongs to the class of compounds known as butyric acid derivatives. It is a colorless liquid with a pungent odor and can be used in pharmaceutical preparations as an antispasmodic or a sedative. 2-Carboxy-3,4-dimethoxybenzaldehyde has been shown to have radical scavenging activities in tissue culture systems and dry weight reaction products in the presence of hydrochloric acid and chloride ion. This compound can also act as an acid complexing agent for hydrogen chloride and depressant activity on animal behavior.

<p>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.</p>

<p>2-Phenoxybenzaldehyde is an organic compound that belongs to the heterocyclic aldehyde family. It is a white solid with a strong, pleasant odor. 2-Phenoxybenzaldehyde is used as an intermediate in organic synthesis, and has been shown to inhibit the receptor activity of human leukocyte antigen (HLA) class II molecules. The reaction mechanism for this inhibition is not known. The reaction of 2-phenoxybenzaldehyde with hydrochloric acid produces phenylhydroxylamine, which can be oxidized by inorganic acids to form phenyloxalic acid. This compound also inhibits the production of inflammatory cytokines such as TNFα and IL-1β in vitro and in vivo.</p>

<p>2,5-Dimethoxy-4-methylbenzaldehyde is a bioactive chemical that has been shown to have anticancer activity. It has been shown to be an effective inhibitor of cancer cell growth in vitro and in vivo. 2,5-Dimethoxy-4-methylbenzaldehyde has also been shown to inhibit the formation of fatty acids and improve the uptake of glucose by cancer cells. This compound is a metabolite of the amino acid methionine and is used as a marker for mesenchymal cells. The structure of 2,5-dimethoxy-4-methylbenzaldehyde consists of two methoxy groups connected with an aliphatic chain consisting of one or more carbon atoms. This functional group may provide the anticancer activity through radical scavenging activities.</p>

<p>3-Hydroxybenzaldehyde (3HBA) is an organic molecule that belongs to the group of substituted benzaldehydes. It has been shown to induce muscle cell proliferation in vitro and in vivo, as well as increased levels of activated caspase-3 in vitro. 3HBA also has a high resistance to hydrochloric acid, hydrogen bond, and chemical structures. It also shows properties of intramolecular hydrogen bonding and aldehyde groups. 3HBA has been shown to be active against malonic acid-induced pulmonary edema in rats, which may be due to its ability to inhibit the release of erythrocytes from the bone marrow into the circulation.</p>

<p>Benzo[b]thiophene-2-carboxaldehyde is a compound that has optical properties with a dihedral angle of 90°. This compound also has a functional group of imine, which can be found in the amino acid histidine. Benzo[b]thiophene-2-carboxaldehyde has been shown to have cancer inhibiting properties by targeting the protease activity of at1 receptors. It inhibits the synthesis of protein and RNA by binding to them and preventing their production. This compound also inhibits the activity of proteases, which are enzymes that break down proteins. Benzo[b]thiophene-2-carboxaldehyde is synthesized through metathesis reactions, which are reactions that involve the exchange of atoms between two compounds. The yield is isolated at about 95%.</p>

<p>1-Methyl-1H-imidazole-4-carbaldehyde is an Imidazole derivative. Imidazoles are the most prominent heterocyclic scaffolds found in medical molecules and natural products. Due to the peculiar structural characteristics of imidazole, it is advantageous for imidazole groups to combine with various receptors and enzymes in biological systems, through diverse weak interactions. 1-Methyl-1H-imidazole-4-carbaldehyde is one of many imidazole derivatives that are used as building blocks for a wide variety of target compounds.</p>

<p>4-Methoxy-2-methylbenzaldehyde (4MMBA) is a synthetic chemical that is used as an antifungal agent. It interacts with the cellular membranes of fungi and disrupts their ability to maintain homeostasis. 4MMBA inhibits the growth of invasive aspergillosis by inhibiting protein synthesis, which leads to cell death. The mechanism of action for 4MMBA is not well understood, but it has been shown to inhibit the growth of fungi in a model system. It also inhibits the production of pyrylium, which may be responsible for its activity against fungi.</p>

<p>2-Fluoro-6-(trifluoromethyl)benzaldehyde is a chemical compound that is used in the synthesis of other organic compounds. It can be synthesized by reacting benzaldehyde with sodium trifluoromethanesulfinate in liquid ammonia solution at a temperature of -78°C. The reaction produces 2-fluoro-6-(trifluoromethyl)benzaldehyde, which is isolated by evaporating the reaction liquid and recrystallizing the product from methanol. The yield of this reaction is high and there are no major byproducts.</p>

<p>2,4,6-Trimethoxybenzaldehyde is a chemical compound that is used as an intermediate in organic chemistry. It has been shown to have antiviral effects on influenza A virus by inhibiting the enzyme neuraminidase. This inhibition prevents the release of viruses from infected cells and thus prevents viral replication. 2,4,6-Trimethoxybenzaldehyde also inhibits the growth of cancer cells in vitro and has minimal toxicity to normal cells. This chemical has been shown to inhibit the reaction mechanism of proton pumps in mammalian cells, which may be due to its ability to inhibit p2y receptors or nitrogen atoms. 2,4,6-Trimethoxybenzaldehyde can also be used as a solvent for pharmaceutical preparations and as a reagent in x-ray diffraction data analysis.</p>

<p>2,3-Dichlorobenzaldehyde oxime is a versatile building block and reagent in the synthesis of complex compounds. It is mainly used as a research chemical and speciality chemical. 2,3-Dichlorobenzaldehyde oxime has been widely used for the preparation of fine chemicals, pharmaceuticals, agrochemicals, and other organic compounds. This compound can be reacted with various reagents to produce useful scaffolds or reaction components.</p>

3-Iodobenzaldehyde is an atypical, isomeric, low energy, functional group. It has a fluorine atom in the 3-position and three different types of functional groups: alcohol, aldehyde and carboxylic acid. This compound has been studied for its ability to bind to receptors. 3-Iodobenzaldehyde can be synthesized by reacting benzalchohde with iodine and hydrochloric acid. The technique used to produce this compound is called Grignard reaction. 3-Iodobenzaldehyde can also be prepared by heating the corresponding nitrobenzene with sodium iodide in dry ether or under refluxing conditions. This compound has a low boiling point and melts at about 170 degrees Celsius. The frequency of this molecule ranges from 98 to 102 megahertz

<p>4-N-Octylbenzaldehyde is a nitro compound which is used as an immunosuppressive agent. It has been shown to inhibit the activity of diphenolase, which plays an important role in the metabolism of fatty acids. 4-N-Octylbenzaldehyde also has an oil extractant that can be used to extract and separate different types of organic compounds from oils, fats, or greases. In addition, 4-N-octylbenzaldehyde inhibits the synthesis of prostaglandin E2 and thromboxane A2 by inhibiting cyclooxygenase enzymes. It has been shown to possess anti-inflammatory properties and has been found to be useful in treating rheumatoid arthritis.</p>

Phloroglucinol aldehyde triethyl ether is a high quality, research chemical, speciality chemical and versatile building block. It is used in the synthesis of complex compounds that are useful as intermediates or fine chemicals. The CAS No. for this compound is 59652-88-9.