Naftalenos
Foram encontrados 2438 produtos de "Naftalenos"
3-(naphthalen-2-yl)-4,5-dihydro-1,2-oxazole-5-carboxylic acid
CAS:Pureza:95.0%Peso molecular:241.24600219726562Benzyl (2S)-4-(7-(8-chloronaphthalen-1-yl)-2-(methylsulfinyl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-yl)-2-(cyanomethyl)piperazine-1-carboxylate
CAS:Pureza:97%Peso molecular:615.15002441406255-[2-(naphthalen-2-yloxy)phenyl]-1H-1,2,3,4-tetrazole
CAS:Pureza:98%Peso molecular:288.309997558593756-Methyl-5-((3-(2-(methylthio)pyrimidin-4-yl)pyridin-2-yl)oxy)naphthalen-1-amine
CAS:Pureza:98%Peso molecular:374.45999145507811-(Naphthalen-2-yl)-3-(2-oxo-2-(pyrrolidin-1-yl)ethyl)urea
CAS:Pureza:98%Peso molecular:297.35800170898441-Naphthylamine
CAS:Applications 1-Naphthylamine is a reagent used to synthesize various dyes used in the textile industry.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Case, R., et al.: Brit. J. Ind. Med., 11, 75 (1954)Fórmula:C10H9NCor e Forma:Light Brown To Light PurplePeso molecular:143.19Naphthalene-d8
CAS:Produto ControladoApplications Naphthalene-d8, is the labeled analogue of Naphthalene, a polycyclic aromatic hydrocarbons as micropollutants.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Di Toro, D., et al.: Environ. Toxicol. Chem., 19, 1971 (2000), Vines, C., et al.: Aquat. Toxicol., 51, 225 (2000), Incardona, J., et al.: Toxicol. Appl. Pharmacol., 196, 191 (2004), Junghans, M., et al.: Aquat. Toxicol., 76, 93 (2006),Fórmula:C10D8Cor e Forma:WhitePeso molecular:136.222-(4-Bromonaphthalen-1-yl)-4,6-diphenyl-1,3,5-triazine
CAS:Pureza:97%Peso molecular:438.3280029296875N-(2-(4-oxo-4H-benzo[d][1,3]oxazin-2-yl)phenyl)naphthalene-2-sulfonamide
CAS:Pureza:97%Cor e Forma:SolidPeso molecular:428.45999145507814-(naphthalene-2-carbonyl)-8-propyl-1-oxa-4,8-diazaspiro[4.5]decane-3-carboxylic acid
CAS:Pureza:95.0%Peso molecular:382.45999145507812-(4-(tert-Butoxycarbonyl)piperazin-1-yl)-2-(naphthalen-2-yl)acetic acid
CAS:Pureza:96%Peso molecular:370.44900512695315-(Naphthalen-2-yl)-1-phenyl-1H-pyrazole-3-carboxylic acid
CAS:Pureza:95.0%Peso molecular:314.343994140625(R)-3-((tert-Butoxycarbonyl)amino)-3-(naphthalen-1-yl)propanoic acid
CAS:Pureza:98%Peso molecular:315.3689880371094Ref: 10-F466812
1gA consultar2gA consultar5gA consultar10gA consultar100mgA consultar250mgA consultar500mgA consultar2-{4-[4-(7-Hydroxy-naphthalen-1-yl)-piperazin-1-yl]-butyl}-4-methyl-2H-[1,2,4]triazine-3,5-dione
Pureza:95.0%Peso molecular:409.4899902343752-Naphthalenesulfonic acid
CAS:2-Naphthalenesulfonic acid is an activated sodium salt that is used to treat wastewater. It has been shown to react with malonic acid, a major component of wastewater, by forming a kinetic and thermodynamic acid complex. The reaction solution then reacts with epidermal growth factor to form benzalkonium chloride. 2-Naphthalenesulfonic acid has been shown to be effective in the treatment of wastewater due to its ability to remove organic materials and inhibit the growth of bacteria.
Fórmula:C10H8SO3Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:208.23 g/mol3,5-Dihydroxy-2-naphthoic acid
CAS:3,5-Dihydroxy-2-naphthoic acid (DHNA) is an organic compound with a red shift in the optical spectrum. DHNA is a regulatory domain found in functional groups, such as salicylic acid. It has been shown to inhibit bacterial growth and gram-negative organisms, including Escherichia coli and Pseudomonas aeruginosa. DHNA is also a potent inducer of triticum aestivum lysine carboxypeptidase A and B, which are proteases that function in protein digestion. This property may be due to its ability to bind to receptor subtypes of the epidermal growth factor type 2 receptor family.Fórmula:C11H8O4Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:204.18 g/mol2-Naphthylacetic acid
CAS:2-Naphthylacetic acid is a molecule that has been shown to inhibit serine proteases in humans and other mammals. It has been tested as a growth regulator for plants and has shown promising results in the prevention of root formation. 2-Naphthylacetic acid can be used to inhibit the activity of hydrogen bonding, which is required for chromatographic methods. The compound's chemical structure includes a naphthalene ring with two acetic acid groups on either side of it.Fórmula:C12H10O2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:186.21 g/mol1-Naphthol dihydrogen phosphate monosodium monohydrate
CAS:1-Naphthol dihydrogen phosphate monosodium salt monohydrate is an organic compound that is a useful scaffold for the synthesis of other organic compounds. It is also used as a reagent and building block in organic synthesis. 1-Naphthol dihydrogen phosphate monosodium salt monohydrate has CAS No. 81012-89-7 and can be used as a reaction component, intermediate, or building block in the synthesis of complex compounds. This compound is soluble in water, ethanol, ethers, benzene, chloroform, and acetone. The purity level of 1-naphthol dihydrogen phosphate monosodium salt monohydrate ranges from 99% to 100%.Fórmula:C10H9O4P•Na•H2OPureza:Min. 98%Cor e Forma:PowderPeso molecular:265.16 g/mol8-Anilino-1-naphthalenesulfonic acid
CAS:8-Anilino-1-naphthalenesulfonic acid is a potent and selective inhibitor of the proteasome. It inhibits the activity of the proteasome and leads to neuronal death. 8-Anilino-1-naphthalenesulfonic acid has been shown to have antioxidative properties in a Langmuir adsorption isotherm study. This compound also has fluorescence, which makes it useful as a fluorescent probe for protein identification in human serum. 8-Anilino-1-naphthalenesulfonic acid binds to proteins with hydrophobic regions, such as lipids and phospholipids, due to its hydrophobic effect. It can be used as an analytical method for determining the protein content in water samples.
Fórmula:C16H13NO3SPureza:Min. 95 Area-%Cor e Forma:Brown Green PowderPeso molecular:299.35 g/molNaphthol AS phosphate
CAS:Naphthol AS phosphate is a food additive that is used as an anti-aromatase agent. It inhibits the enzyme aromatase, which converts androgens to estrogens. This inhibition prevents the development of estrogen-dependent cancers such as breast cancer in women and prostate cancer in men. Naphthol AS phosphate also has inhibitory effects on inflammatory diseases and other diseases involving cell proliferation.Fórmula:C17H14NO5PPureza:Min. 95%Cor e Forma:PowderPeso molecular:343.27 g/mol1-Hydroxy-2-naphthoic acid
CAS:1-Hydroxy-2-naphthoic acid is a chemical compound that belongs to the group of carboxylic acids. It is used in the treatment of malonic acidemia and as a reagent for the structural analysis of organic compounds. 1-Hydroxy-2-naphthoic acid has been shown to react with protonated malonic acid in a synchronous fluorescence experiment. The reaction mechanism involves an intramolecular hydrogen transfer from the carboxylate group to the naphthalene ring, leading to formation of a methyl ethyl cation. This cation can then either react with another malonic acid molecule or be deprotonated by water, depending on pH and concentration. 1-Hydroxy-2-naphthoic acid has also shown photochemical properties and can be used for wastewater treatment due to its ability to degrade organic pollutants such as phenols and amines.Fórmula:C11H8O3Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:188.18 g/molNaphthalene-1,4,5,8-tetracarboxylic dianhydride
CAS:Naphthalene-1,4,5,8-tetracarboxylic dianhydride is a molecule that contains two carboxylic acid groups and one tetracarboxylic acid group. It is an adsorbent material that is used to remove water vapor from the atmosphere. Naphthalene-1,4,5,8-tetracarboxylic dianhydride is also used in wastewater treatment processes because it has high chemical stability and can be regenerated with anhydrous sodium. The transport properties of naphthalene-1,4,5,8-tetracarboxylic dianhydride are well suited for use as a model system for studying the kinetics of proton exchange membrane fuel cells (PEMFC). This compound has been studied using electrochemical impedance spectroscopy to determine its kinetic data.Fórmula:C14H4O6Pureza:Min. 95 Area-%Cor e Forma:Off-White PowderPeso molecular:268.18 g/molAzomethine-H monosodium salt monohydrate
CAS:Azomethine-H is a research chemical that is used as a versatile building block for the synthesis of other compounds. It has been shown to be an intermediate in the synthesis of many complex compounds, and can also be used as a reagent or speciality chemical. Azomethine-H is soluble in water and organic solvents, which makes it useful for reactions involving deprotection, extraction, or alkylation. The CAS registry number for this compound is 304655-82-1.Fórmula:C17H12NNaO8S2·H2OPureza:Min. 95.0 Area-%Cor e Forma:Yellow PowderPeso molecular:463.42 g/mol1-Naphthol
CAS:Derivative of naphthalene; used in the synthesis of various chemicals and as a precursor in the production of dyes, pigments, and pharmaceuticals. It is particularly important in the manufacture of azo dyes, where it serves as a coupling agent in the diazo coupling reaction to produce colored compounds.Fórmula:C10H7OHPureza:Min. 95%Cor e Forma:PowderPeso molecular:144.17 g/mol2-Chloronaphthalene
CAS:2-Chloronaphthalene is a polychlorinated naphthalene that has been shown to be an effective inducer of p450 activity, which is a cytochrome P450 enzyme. 2-Chloronaphthalene is also a structural analog of the polychlorinated biphenyls (PCBs), and has been shown to have similar toxic effects on the liver. 2-Chloronaphthalene is used as an intermediate in organic synthesis and as a precursor for other compounds. It can be used to synthesize malonic acid, which can be reacted with sodium hydroxide or carbon disulfide to produce polymeric matrices such as polyvinyl chloride.
Fórmula:C10H7ClPureza:Min. 95%Cor e Forma:Colourless Or White To Pink SolidPeso molecular:162.62 g/mol(R)-1,1'-Bi-2-Naphthol
CAS:(R)-1,1'-Bi-2-Naphthol is an organic compound that is made from the hydrogenation of 2-naphthol. The sodium salts of this compound are chiral and can be used to synthesize racemic mixtures with a high degree of optical purity. The x-ray crystal structures of (R)-1,1'-Bi-2-Naphthol have been studied in detail and show that this molecule exhibits intermolecular hydrogen bonding interactions. It also has a steric interaction with the amine group which prevents rotation about the C3—C4 bond. Other interesting features include intramolecular hydrogen bonding interactions between the hydroxyl group and the alkanoic acid. This molecule also has a hydrophobic region consisting of three methyl groups that are connected to fatty acids.Fórmula:C20H14O2Pureza:Min. 98.5 Area-%Cor e Forma:White Off-White PowderPeso molecular:286.32 g/mol1-Naphthoic acid
CAS:1-Naphthoic acid is a phenolic antioxidant that is used in the treatment of inflammatory bowel disease. It has been shown to reduce the production of inflammatory cytokines and improve symptoms of bowel disease. 1-Naphthoic acid, as a fluorescence probe, can be used to detect and quantify hydroxycinnamic acids in biological fluids such as serum and urine. 1-Naphthoic acid also inhibits serine protease activity, which is involved in autoimmune diseases such as lupus erythematosus. It also inhibits the activity of hydrolytic enzymes that are associated with metabolic disorders such as diabetes mellitus. In addition, 1-naphthoic acid can act as an agonist at certain receptors including muscarinic receptors and α2A receptors. It has also been shown to increase levels of retinoic acid and inhibit the formation of hydrogen peroxide by bacteria like H. pylori due to its abilityFórmula:C11H8O2Pureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:172.18 g/molPamoic acid
CAS:Pamoic acid is a natural compound that has been found to exhibit antimicrobial activity against a variety of microorganisms. Pamoic acid is also used in the treatment of infectious diseases, such as leprosy, tuberculosis, and AIDS. The biological properties of pamoic acid are due to its ability to bind with peptide hormones and act as a pharmacological agent. Pamoic acid is able to inhibit the synthesis of peptide hormones by binding to their receptors on the cell surface. This inhibition can lead to immunosuppression (e.g., autoimmune diseases) and mitochondrial membrane depolarization. Pamoic acid is also able to bind with benzalkonium chloride, which may account for some of its antimicrobial activity.
Pamoic acid is synthesized from pantothenic acid (vitamin B5) and caproic acid by means of an enzymatic process called transamination.Fórmula:C23H16O6Pureza:Min. 95%Cor e Forma:Yellow PowderPeso molecular:388.37 g/mol2-Naphthaldehyde
CAS:2-Naphthaldehyde is an antimicrobial agent that has been shown to inhibit the growth of bacteria in vitro. It has been shown to inhibit the synthesis of DNA, RNA and protein. 2-Naphthaldehyde is an intramolecular hydrogen acceptor and a substrate for coumarin derivatives. The reaction mechanism of 2-napthalaldehyde is not yet fully understood, but it has been proposed that 2-napthalaldehyde reacts with sodium carbonate to form sodium phenolate and acetone. 2-Naphthaldehyde also shows genotoxic activity, as it has been shown to induce structural aberrations in bacterial DNA. This chemical compound also forms coordination geometry complexes with metal ions such as copper and zinc.Fórmula:C11H8OPureza:Min. 98%Cor e Forma:Beige PowderPeso molecular:156.18 g/mol
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