Building Blocks
Esta sección contiene productos fundamentales para la síntesis de compuestos orgánicos y biológicos. Building blocks son los materiales de partida esenciales utilizados para construir moléculas complejas a través de diversas reacciones químicas. Desempeñan un papel crítico en el descubrimiento de fármacos, la ciencia de materiales y la investigación química. En CymitQuimica, ofrecemos una gama diversa de building blocks de alta calidad para apoyar sus investigaciones innovadoras y proyectos industriales, asegurando que tenga los componentes esenciales para una síntesis exitosa.
Subcategorías de "Building Blocks"
- Ácidos borónicos y derivados del ácido borónico(5.778 productos)
- Building Blocks quirales(1.243 productos)
- Building Blocks de hidrocarburos(6.097 productos)
- Building Blocks orgánicos(61.048 productos)
Se han encontrado 203115 productos de "Building Blocks"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Furo[2,3-b]pyridin-3(2H)-one
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C7H5NO2Pureza:Min. 95%Peso molecular:135.12 g/mol3-(2-Bromoacetyl)pyridin-2(1H)-one
CAS:Versatile small molecule scaffoldFórmula:C7H6BrNO2Pureza:Min. 95%Peso molecular:216.03 g/mol2-Methyl-6-oxo-1,4,5,6-tetrahydropyridine-3-carbonitrile
CAS:Versatile small molecule scaffoldFórmula:C7H8N2OPureza:Min. 95%Peso molecular:136.15 g/mol4-Hydroxy-2,5-dimethylbenzoic acid
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C9H10O3Pureza:Min. 95%Peso molecular:166.17 g/mol2-Amino-2-(furan-2-yl)ethan-1-ol
CAS:Versatile small molecule scaffoldFórmula:C6H9NO2Pureza:Min. 95%Peso molecular:127.14 g/mol2-(2-Amino-1-hydroxyethyl)furan
CAS:Versatile small molecule scaffoldFórmula:C6H9NO2Pureza:Min. 95%Peso molecular:127.14 g/molIsopropoxybenzene
CAS:<p>Isopropoxybenzene is an organic compound that belongs to the group of alkynylbenzenes. It is synthesized from ethyl diazoacetate and a terminal alkoxybenzene in the presence of a Friedel-Crafts catalyst. Isopropoxybenzene has been found to have potent anti-inflammatory effects and can be used for the treatment of bowel disease, such as ulcerative colitis. The biological properties of isopropoxybenzene are related to its ability to act as a potent antagonist of chloride channels. Isopropoxybenzene also has the potential to inhibit production of inflammatory factors by reducing oxidative stress in cells.</p>Fórmula:C9H12OPureza:Min. 95%Peso molecular:136.19 g/mol1-Benzyl-3,3-dimethylthiourea
CAS:Versatile small molecule scaffoldFórmula:C10H14N2SPureza:Min. 95%Peso molecular:194.3 g/mol3-Methyl-1-(naphthalen-1-yl)thiourea
CAS:Versatile small molecule scaffoldFórmula:C12H12N2SPureza:Min. 95%Peso molecular:216.3 g/mol1-Fluoro-4-(2-isothiocyanatoethyl)benzene
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C9H8FNSPureza:Min. 95%Peso molecular:181.23 g/mol1-(Isothiocyanatomethyl)-3-(trifluoromethyl)benzene
CAS:Versatile small molecule scaffoldFórmula:C9H6F3NSPureza:Min. 95%Peso molecular:217.21 g/mol2-Chlorophenyl Isothiocyanate
CAS:<p>2-Chlorophenyl Isothiocyanate is a molecule that has been shown to have cytotoxic activity against cancer cells. It is believed to work by inducing apoptosis and modulating the expression of certain genes. 2-Chlorophenyl Isothiocyanate has also been shown to induce cell death in fibroblast cells, which may be due to its ability to polarize these cells and cause them to become more susceptible to oxidative stress. It also has the ability to react with DNA via a dihedral mechanism. The thermodynamic data for this compound are high, as it can form strong hydrogen bonds and hydrophilic interactions with water molecules. This molecule also contains functional groups such as carbonyl and thiocarbonyl, which are reactive in biological systems. 2-Chlorophenyl Isothiocyanate's reaction mechanism is believed to involve electron transfer from an electron rich site on the molecule (such as a carbonyl)</p>Fórmula:C7H4ClNSPureza:Min. 95%Peso molecular:169.63 g/molOctaahydro-indolizin-3-one
CAS:Octahydro-indolizin-3-one is a peptidomimetic with a hypervalent structure. It has been shown to bind to the pancreatic enzyme cck-a with high affinity, and it can inhibit the production of proinflammatory cytokines. Octahydro-indolizin-3-one has also been shown to be selective for the receptor subtype that binds amido groups, which is important for its activity. This compound also shows stereoselectivity in binding to ornithine, which may be responsible for its biological activities.Fórmula:C8H13NOPureza:Min. 95%Peso molecular:139.19 g/mol1,2,3,4-Tetrahydroquinoline-1-carbaldehyde
CAS:<p>Tetrahydroquinoline-1-carbaldehyde is extracted from the seeds of the plant Cyperus rotundus. It has been shown to have trackable results in laboratory mice.</p>Fórmula:C10H11NOPureza:Min. 95%Peso molecular:161.2 g/molEthyl(3-methylbutan-2-yl)amine hydrochloride
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C7H18ClNPureza:Min. 95%Peso molecular:151.68 g/mol7-Hydroxy-8-methyl-2H-1-benzopyran-2-one
CAS:The 7-hydroxy-8-methyl-2H-1-benzopyran-2-one is a fluorescent probe that is used in the imaging of DNA and RNA. It has been shown to bind to nucleic acids with high affinity, and can be used to identify the location of specific sequences on DNA or RNA. The fluorescence of this probe can be detected using a microscope, which makes it useful for identifying specific regions of DNA or RNA.Fórmula:C10H8O3Pureza:Min. 95%Peso molecular:176.17 g/mol2-(4-Fluorophenyl)-1-(4-methoxyphenyl)ethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C15H13FO2Pureza:Min. 95%Peso molecular:244.26 g/mol1-Bromo-3-((trifluoromethyl)sulfonyl)benzene
CAS:<p>Versatile small molecule scaffold</p>Fórmula:C7H4BrF3O2SPureza:Min. 95%Peso molecular:289.07 g/mol5-tert-Butyl-2-hydroxybenzaldehyde
CAS:<p>5-tert-Butyl-2-hydroxybenzaldehyde is a synthetic compound that has been used in wastewater treatment. It is a hydrogen donor, which helps to remove organic matter and other contaminants from wastewater. The hydrogen bonding properties of 5-tert-Butyl-2-hydroxybenzaldehyde have been studied systematically using hydrogen chloride and hydrogen ions. This compound reacts with the acidic ph, removing hydrogen ions and forming chloride. The fluorescence lifetimes of this compound have been shown to vary with structural changes. Oxidation products of 5-tert-Butyl-2-hydroxybenzaldehyde have also been synthesized, studied crystallographically, and structurally characterized.</p>Fórmula:C11H14O2Pureza:Min. 95%Peso molecular:178.23 g/mol1-Methyl-3-phenyl thiourea
CAS:1-Methyl-3-phenyl thiourea is a homologous compound that has been shown to produce an increase in cerebral blood flow and a decrease in hematocrit. 1-Methyl-3-phenyl thiourea also has an empirically derived rat dose, which is 100 mg/kg. This drug has been shown to produce dihedral angles of approximately 180 degrees and unsymmetrical conformation. 1-Methyl-3-phenyl thiourea is a good example of a molecule with centrosymmetrical conformation.Fórmula:C8H10N2SPureza:Min. 95%Peso molecular:166.24 g/mol
