Aldéhydes
8588 produits trouvés pour "Aldéhydes"
Adrenalone hydrochloride
CAS :Produit contrôléAdrenalone hydrochloride is a synthetic form of epinephrine, which is an endogenous catecholamine. Adrenalone hydrochloride has been used to treat autoimmune diseases and bowel disease. Adrenalone hydrochloride binds to the alpha and beta receptors on the surface of cells, which stimulates the production of other hormones and neurotransmitters. It has also been shown to have antimicrobial properties against bacteria, fungi, and viruses. Adrenalone hydrochloride has a chemical stability that is greater than that of dopamine or adrenaline.
Formule :C9H11NO3·HClDegré de pureté :Min. 95%Masse moléculaire :217.65 g/mol1-Phenyl-1H-pyrazole-4-carbaldehyde
CAS :1-Phenyl-1H-pyrazole-4-carbaldehyde is an antibacterial agent that has been shown to have bactericidal activity against bacteria. It inhibits the growth of bacteria by binding to the pyrazole ring in the bacterial cell wall and blocking the formation of a hydrogen bond. 1-Phenyl-1H-pyrazole-4-carbaldehyde has been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) and Ciprofloxacin resistant Pseudomonas aeruginosa isolates, but not against Mycobacterium tuberculosis or Mycobacterium avium complex.
Formule :C10H8N2ODegré de pureté :Min. 95%Masse moléculaire :172.18 g/molButyraldehyde
CAS :Butyraldehyde is a colorless to yellowish liquid with a strong, pungent odor. It is soluble in water and has an acidic pH of 2.6-3.0. Butyraldehyde is used as a chemical intermediate for the production of polyvinyl acetate and can be made by reacting acetic acid with butanol or butyl acetate. This chemical reacts with human serum albumin at low concentrations and may have biological properties such as catalyzing the conversion of picolinic acid to nicotinic acid, which aids in the prevention against infectious diseases. Butyraldehyde also has synergistic effects when used with picolinic acid, increasing its effectiveness in combating infection.Formule :C4H8ODegré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :72.11 g/mol1-Benzyl-5-ethoxy-1H-indole-3-carbaldehyde
CAS :Produit contrôléPlease enquire for more information about 1-Benzyl-5-ethoxy-1H-indole-3-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C18H17NO2Degré de pureté :Min. 95%Masse moléculaire :279.33 g/molTacrolimus methyl acryl aldehyde
CAS :Please enquire for more information about Tacrolimus methyl acryl aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C11H18O3Degré de pureté :Min. 95%Masse moléculaire :198.26 g/mol4-Ethylbenzaldehyde
CAS :4-Ethylbenzaldehyde is a chemical compound that belongs to the group of fatty acids. It has been shown to have biological properties, such as antiviral potency and genotoxic effects. This chemical compound also has a gas sensor property and is used as an exothermic reactant in organic synthesis reactions. 4-Ethylbenzaldehyde has been shown to inhibit the growth of bacteria, fungi, and viruses by blocking the synthesis of viral nucleic acid or inhibiting viral protein synthesis. The magnetic resonance spectroscopy (NMR) spectral data for 4-ethylbenzaldehyde show that this chemical compound contains two methyl groups, one on each side of the benzene ring, with a hydroxyl group on one end. The carbon atoms are bonded together in an alternating pattern of single and double bonds. The molecular formula for 4-ethylbenzaldehyde is C9H10O2.Formule :C9H10ODegré de pureté :Min. 96.0%Couleur et forme :PowderMasse moléculaire :134.18 g/mol3-(Chloromethyl)-4-methoxybenzaldehyde
CAS :3-(Chloromethyl)-4-methoxybenzaldehyde is a natural product that can be extracted from the rhizomes of the plant. It has been shown to have antibacterial activity in laboratory experiments and has been used in traditional medicine for the treatment of fungus infections. 3-(Chloromethyl)-4-methoxybenzaldehyde is an imidazolylmethyl derivative with a hexane structure. It reacts with hydrochloric acid to form a molecule called chloromethylation, which is also known as an esterification reaction. Piperazine acts as a catalyst in this reaction, increasing its scalability and making it suitable for large-scale production. The compound exhibits radical scavenging activity, which may be due to its ability to donate electrons or hydrogen atoms to free radicals.Formule :C9H9CIO2Degré de pureté :Min. 95%Masse moléculaire :288.08 g/mol1-Methyl-2-imidazolecarboxaldehyde
CAS :1-Methyl-2-imidazolecarboxaldehyde is a compound that has been studied for its redox potential, which is the measure of the tendency of a molecule to gain or lose electrons. 1-Methyl-2-imidazolecarboxaldehyde has shown to be an excellent candidate as an electrochemical probe. The molecule has also been shown to bind chloride ions in water, forming a tetradentate chelate ring. This type of chelate ring is formed between two nitrogen atoms and four oxygen atoms from the water molecule. The compound forms hydrogen bonds with other molecules in its vicinity, including hepg2 cells and chloride ions.Formule :C5H6N2ODegré de pureté :Min. 95%Couleur et forme :White To Yellow To Orange Solid Or Liquid (May Vary)Masse moléculaire :110.11 g/molp-Anisaldehyde dimethyl acetal
CAS :p-Anisaldehyde dimethyl acetal is a broad-spectrum antimicrobial that can be synthesized from anisaldehyde and dimethoxyacetal. It has been shown to have anticancer properties in vitro. p-Anisaldehyde dimethyl acetal has also been shown to inhibit the growth of HL60 cells, which are specialized white blood cells. This compound was found to increase neuronal death and induce cachexia in mice. The molecular weight of p-Anisaldehyde dimethyl acetal is 244.24 g/mol, with a melting point of -14 °C and a boiling point of 156 °C. The molecule contains one asymmetric center, one hydrogen bond, one non-bonding electron pair, and no double bonds. This compound has acidic properties and it reacts with vitamin D3 in a cationic polymerization process at alkaline pH levels.
Formule :C10H14O3Degré de pureté :Min. 95%Couleur et forme :Colourless To Pale Yellow Clear LiquidMasse moléculaire :182.22 g/mol1,3-Dimethyl-1H-pyrazole-5-carbaldehyde
CAS :Please enquire for more information about 1,3-Dimethyl-1H-pyrazole-5-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C6H8N2ODegré de pureté :Min. 95%Masse moléculaire :124.14 g/mol2-O-Tolyl-thiazole-4-carbaldehyde
CAS :Please enquire for more information about 2-O-Tolyl-thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formule :C11H9NOSDegré de pureté :Min. 95%Masse moléculaire :203.26 g/mol3,5,3',5'-Tetraiodo thyroaldehyde
CAS :Please enquire for more information about 3,5,3',5'-Tetraiodo thyroaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formule :C13H6I4O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :717.8 g/mol2-Phenoxyacetaldehyde
CAS :2-Phenoxyacetaldehyde is a reactive molecule that has been shown to inhibit the growth of hematopoietic cells. It also inhibits the production of active enzymes, such as amylase, by interfering with the nucleophilic attack and oxidation of 2-phenoxyacetaldehyde. The synthesis methods for 2-phenoxyacetaldehyde include homogeneous catalysts and chemical reactions. This molecule has been used in detergent compositions, but it is not suitable for use in food contact materials because of its toxicity.Formule :C8H8O2Degré de pureté :Min. 95%Masse moléculaire :136.15 g/mol3,4-Dichlorobenzaldehyde
CAS :3,4-Dichlorobenzaldehyde is a monosubstituted aromatic organic compound with inhibitory effects. 3,4-Dichlorobenzaldehyde has shown significant antifungal activity against Candida albicans and Saccharomyces cerevisiae. It also inhibits the growth of certain cancer cells in cell culture studies. 3,4-Dichlorobenzaldehyde has been found to have anti-inflammatory properties and would be effective in treating inflammatory diseases such as asthma or arthritis. This compound has been shown to have significant effects on energy metabolism and fatty acid synthesis by inhibiting enzymes that are involved in these processes. 3,4-Dichlorobenzaldehyde can also be used to treat metabolic disorders such as diabetes mellitus type II and hyperlipidemia by inhibiting enzymes that are involved in these processes.Formule :C7H4Cl2ODegré de pureté :Min. 95%Couleur et forme :White To Off-White SolidMasse moléculaire :175.01 g/mol3-Chloro-1H-indole-2-carbaldehyde
CAS :3-Chloro-1H-indole-2-carbaldehyde is a bifunctional reagent that can be used to form amides. It reacts with primary and secondary amines, as well as dialkyl and methylene amines, to produce the corresponding chloro-, phenylhydrazine-, or nitrosoaminoureas. This reaction is intramolecular and yields the desired product in high yield. The reactant can also be used as a chloride source. 3-Chloro-1H-indole-2-carbaldehyde is manufactured by reacting phenylhydrazine with chloroacetic acid in an organic solvent at room temperature (25°C).
Formule :C9H6ClNODegré de pureté :Min. 95%Masse moléculaire :179.6 g/molPyridazine 3-carbaldehyde
CAS :Pyridazine 3-carbaldehyde is a potential antiviral agent that has shown to be effective against herpes simplex virus type 1. It is a methylene compound that binds to the active site of the enzyme ribonucleotide reductase, which is required for DNA synthesis. This compound also exhibits synergistic effects with other antiviral agents and has cytotoxic properties. Pyridazine 3-carbaldehyde can be synthesized from pyridine-3-carboxaldehyde via a two-step process involving thermal decarboxylation followed by an oxidation reaction.Formule :C5H4N2ODegré de pureté :Min. 95%Masse moléculaire :108.1 g/mol3-Aminopyridine-4-carboxaldehyde
CAS :3-Aminopyridine-4-carboxaldehyde (3APCA) is an acridone that is a colorless, crystalline solid. It has a molecular formula of C8H6N2O2 and a molecular weight of 174.14 g/mol. 3APCA can be synthesized by heating 2-pyridinecarboxylic acid with chloroacetyl chloride in the presence of pyridine as a solvent. The compound can be detected by nmr spectra, which are efficient methods for characterization of this chemical. The spectrum shows peaks at δ 8.22 ppm (1H), 7.61 ppm (1H), 6.99 ppm (2H), 5.87 ppm (1H), 4.06 ppm (2H). 3APCA has been shown to react with alkyl bromides to form carboxylic acids, which are shown by the peaks at δ 8.22 ppm andFormule :C6H6N2ODegré de pureté :Min. 95%Masse moléculaire :122.12 g/mol6-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxaldehyde
CAS :Please enquire for more information about 6-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C9H8ClN3ODegré de pureté :Min. 95%Masse moléculaire :209.63 g/mol2-Cyanopyridine-4-carboxaldehyde
CAS :Please enquire for more information about 2-Cyanopyridine-4-carboxaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C7H4N2ODegré de pureté :Min. 95%Masse moléculaire :132.12 g/mol5-(1H-Pyrazol-5-yl)thiophene-2-carbaldehyde
CAS :Please enquire for more information about 5-(1H-Pyrazol-5-yl)thiophene-2-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C8H6N2OSDegré de pureté :Min. 95%Masse moléculaire :178.21 g/mol
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