Building Blocks
Subcategorías de "Building Blocks"
- Ácidos borónicos y derivados del ácido borónico(5.778 productos)
- Building Blocks quirales(1.243 productos)
- Building Blocks de hidrocarburos(6.099 productos)
- Building Blocks orgánicos(61.038 productos)
Se han encontrado 205376 productos de "Building Blocks"
N-(2-Phenylethyl)benzenesulfonamide
CAS:N-(2-Phenylethyl)benzenesulfonamide is a biodegradable and aerobic catalyst that is used in the production of nitrates. It can be recycled and has a high solubility, which allows for efficient extraction from wastewater effluents. The reactor system can be operated at an aerobic or anaerobic conditions. N-(2-Phenylethyl)benzenesulfonamide is soluble in water and can be hydrolyzed by acids or bases to release ammonia gas. The process can also be sustainable due to the use of renewable energy sources such as solar, wind, tidal, or biomass power.
Fórmula:C14H15NO2SPureza:Min. 95%Peso molecular:261.34 g/mol2-[Ethyl(propan-2-yl)amino]ethan-1-ol
CAS:Producto controladoVersatile small molecule scaffold
Fórmula:C7H17NOPureza:Min. 95%Peso molecular:131.22 g/mol3-Bromo-2-(methylthio)pyridine
CAS:Versatile small molecule scaffold
Fórmula:C6H6BrNSPureza:Min. 95%Peso molecular:204.09 g/mol2-Methylbenzene-1,3-dicarbaldehyde
CAS:2-Methylbenzene-1,3-dicarbaldehyde is a divalent hydrocarbon that has an oxidation catalyst. This compound is used as an intermediate in the production of drugs and pharmaceuticals. It has been shown to have cardiovascular disorders, such as vasodilatation and hypotension. The mechanism of action is not fully understood but may be related to its ability to act as a nitrovasodilator by increasing nitric oxide (NO) release. 2-Methylbenzene-1,3-dicarbaldehyde also produces psychotic disorders when long term exposure occurs. This compound has been shown to have neurotoxic effects in animal models with long term exposure.
Fórmula:C9H8O2Pureza:Min. 95%Peso molecular:148.16 g/mol4-Acetylmorpholine
CAS:4-Acetylmorpholine is a recycled amide that is synthesized from an alkanolamine and an acylation reaction. It has been used in the dehydrating of organic compounds, such as reaction solution, and for the preparation of acrylamide. 4-Acetylmorpholine is also used as a viscosity control agent in the extraction of aromatic hydrocarbons. Its chemical structure consists of a carbonyl group and an aromatic hydrocarbon. 4-Acetylmorpholine can be synthesized by reacting acetaldehyde with ammonia or thiourea with methyl chloride or ethylene oxide.
Fórmula:C6H3D8NO2Pureza:Min. 95%Peso molecular:137.21 g/mol4-Hydroxy-2-naphthoic acid
CAS:4-Hydroxy-2-naphthoic acid is a hydrocarbon with a carboxylic acid group. It can act as an antagonist to the hydrocarbon receptor (HCR). 4-Hydroxy-2-naphthoic acid has been shown to be effective in treating colon cancer cells in vitro, and has been shown to inhibit the growth of cancer cells in vivo. This compound is also effective at inhibiting the proliferation of human colon cancer cells (Caco2) that have been exposed to benzo(a)pyrene, an aromatic hydrocarbon found in cigarette smoke. The mechanism by which this drug inhibits cell proliferation is not fully understood but may involve inhibition of cytochrome P450 1A1 (CYP1A1), which metabolizes benzo(a)pyrene into carcinogenic intermediates. 4-Hydroxy-2-naphthoic acid has also been shown to be anisotropic and microreactor, meaning
Fórmula:C11H8O3Pureza:Min. 95%Peso molecular:188.17 g/mol3-Fluorobenzene-1-sulfonyl fluoride
CAS:3-Fluorobenzene-1-sulfonyl fluoride is a chemical compound that can be used as a catalyst to synthesize organic compounds. It is a colorless liquid, which is soluble in water and organic solvents. This catalyst has been shown to be more efficient than the traditional catalysts, such as tetraphenylphosphonium chloride, potassium fluoride or sodium borohydride. 3-Fluorobenzene-1-sulfonyl fluoride also reacts with nitro groups to produce dinitro compounds, which are valuable synthetic intermediates for the production of dyes and pharmaceuticals. The synthesis of this compound can be carried out in high yields with stoichiometric amounts of reactants.
Fórmula:C6H4F2O2SPureza:Min. 95%Peso molecular:178.16 g/molN-(2-Chlorophenyl)-2-(2-ethoxy-4-formylphenoxy)acetamide
CAS:Versatile small molecule scaffold
Fórmula:C17H16ClNO4Pureza:Min. 95%Peso molecular:333.8 g/mol2-(6-Aminopyridin-2-yl)acetonitrile
CAS:Versatile small molecule scaffold
Fórmula:C7H7N3Pureza:Min. 95%Peso molecular:133.15 g/molRef: 3D-ARA77668
Producto descatalogado4-(3,4,5-Trifluorophenyl)benzoic acid
CAS:Versatile small molecule scaffold
Fórmula:C13H7F3O2Pureza:Min. 95%Peso molecular:252.19 g/mol4-(2,4-Dichlorophenoxy)benzoic acid
CAS:Versatile small molecule scaffold
Fórmula:C13H8Cl2O3Pureza:Min. 95%Peso molecular:283.1 g/mol(4-Aminopyridin-2-yl)methanol
CAS:Versatile small molecule scaffold
Fórmula:C6H8N2OPureza:Min. 95%Peso molecular:124.14 g/mol5,6-Dimethylpyridazin-3(2H)-one
CAS:Versatile small molecule scaffold
Fórmula:C6H8N2OPureza:Min. 95%Peso molecular:124.14 g/mol1-Cyclobutyl-2-methylpropan-1-one
CAS:Versatile small molecule scaffold
Fórmula:C8H14OPureza:Min. 95%Peso molecular:126.2 g/mol1,1,1-Trifluoro-3-methylbutan-2-ol
CAS:Versatile small molecule scaffold
Fórmula:C5H9F3OPureza:Min. 95%Peso molecular:142.12 g/mol2-(4-Fluorophenyl)acetamide
CAS:2-(4-Fluorophenyl)acetamide (FFAA) is a broad-spectrum antiviral drug that has been evaluated against picornavirus, enterovirus, and rhinovirus. FFAA has been shown to be effective in the treatment of acute enterovirus infections in mice. This compound was also found to have a cytopathic effect on cells infected with enteroviruses in culture. It binds to the virus's RNA-dependent RNA polymerase and prevents viral replication. FFAA is not active against influenza A or B viruses, but it is active against influenza C virus. This compound has also been found to have medicinal properties, as it can inhibit the growth of human lung cancer cells in culture and may be useful for treating cancers such as leukemia.
Fórmula:C8H8FNOPureza:Min. 95%Peso molecular:153.15 g/molBenzo[d][1,2,3]thiadiazole
CAS:Benzo[d][1,2,3]thiadiazole is a benzothiadiazole with a redox potential of -0.25 V that is stable in the absence of oxygen and light. It can be used to synthesize chemical pesticides by reacting with hydrochloric acid. The reaction mechanism of benzo[d][1,2,3]thiadiazole has been determined using nuclear magnetic resonance spectroscopy and quantum chemical calculations. This compound reacts with hydrogen bond acceptors on the enzyme active site to form covalent bonds. It also interacts with the enzyme's steric environment by forming hydrogen bonds and van der Waals forces. Benzo[d][1,2,3]thiadiazole also emits light when it reacts with nitric oxide in solution.
Fórmula:C6H4N2SPureza:Min. 95%Peso molecular:136.17 g/moltert-Butyl (2,2-difluoro-3-hydroxypropyl)carbamate
CAS:Versatile small molecule scaffoldFórmula:C10H13NO4Pureza:Min. 95%Peso molecular:211.21 g/mol1-Hydroxycyclopentane-1-carbonitrile
CAS:1-Hydroxycyclopentane-1-carbonitrile is a monomer that is hydrolyzed to form benzoin and cyanohydrins. It can be used in the production of scifinder as a monomer or dimerizer.
Fórmula:C6H9NOPureza:Min. 95%Peso molecular:111.14 g/mol4,5-Dihydro-1H-imidazol-2-amine hydrochloride
CAS:Please enquire for more information about 4,5-Dihydro-1H-imidazol-2-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C3H7N3•HClPureza:Min. 95%Peso molecular:121.57 g/molRef: 3D-FD183639
Producto descatalogado2-Bromo-3,3,3-trifluoro-1-propene
CAS:Producto controlado2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.
Fórmula:C3H2BrF3Pureza:Min. 95%Forma y color:Colorless PowderPeso molecular:174.95 g/mol8-Bromo-2-methylimidazo[1,2-a]pyridine
CAS:Versatile small molecule scaffold
Fórmula:C8H7N2BrPureza:Min. 95%Peso molecular:211.05 g/mol3-Hydroxy-5-methylpyridine
CAS:3-Hydroxy-5-methylpyridine (3HMP) is a chemical substance that has been classified as an amine. It is a product of the metabolism of purines, which are nitrogenous bases found in DNA and RNA. 3HMP is produced by aerogenic bacteria (such as Enterobacter), and can be used to estimate the number of these bacteria present in water samples. 3HMP has been shown to have antiviral properties against influenza virus, and can be used as a biomarker for the presence of other viruses in animals. 3HMP also has mineralization properties, which have been studied extensively, particularly with regards to pancreatic disease.
Fórmula:C6H7NOPureza:Min. 95%Forma y color:PowderPeso molecular:109.13 g/molRef: 3D-FH16174
Producto descatalogado4-Chloro-2-hydroxy-6-methylphenylboronic acid
CAS:Versatile small molecule scaffoldFórmula:C7H8BClO3Pureza:Min. 95%Peso molecular:186.4 g/mol4,5-Dihydroxy-2,3-Pentanedione
CAS:4,5-Dihydroxy-2,3-pentanedione is a carbonyl compound that is the product of the oxidation of ascorbic acid. It is used in wastewater treatment and has antimicrobial properties against infectious diseases. This compound has been shown to inhibit protein synthesis by binding to the ribosome and preventing the formation of peptide bonds between amino acids. 4,5-Dihydroxy-2,3-pentanedione has also been shown to bind to plasma proteins, which may be due to its acyl chain structure. 4,5-Dihydroxy-2,3-pentanedione can be synthesized in a catalytic mechanism that involves dehydroascorbic acid and molecular oxygen.
Fórmula:C5H8O4Pureza:Min. 95%Forma y color:PowderPeso molecular:132.11 g/molRef: 3D-FD180770
Producto descatalogadoPiperyline
CAS:Piperyline is an alkanoic acid that has shown to be effective against skin cancer. It also has antimicrobial properties, which may be due to its ability to bind metal ions and form polymeric compounds. Piperyline inhibits microbial growth by inhibiting the synthesis of proteins and nucleic acids. The antimicrobial activity is related to its cationic polymerization with hydroxyl groups, which forms a structure that can inhibit microbial enzymes and disrupt microbial cell membranes. This compound also interacts with the skin's natural lipids, making it difficult for microorganisms to attach and grow on the skin. Piperyline is synthesized in organic chemistry laboratories as an amide precursor of other pharmaceuticals such as penicillin.
Fórmula:C16H17NO3Pureza:Min. 95%Peso molecular:271.31 g/mol
