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
- Building Blocks quirales
- Building Blocks de hidrocarburos
- Building Blocks orgánicos
Productos de "Building Blocks"
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2-Phenylpent-4-en-1-amine
CAS:Producto controlado2-Phenylpent-4-en-1-amine is an organic compound that is synthesized by the bond cleavage of an amine and a terminal alkyne. It has been used in ligand design, which is the process of creating molecules to bind to a specific biological target. 2-Phenylpent-4-en-1-amine can be used as a chiral catalyst for asymmetric synthesis, making it enantiopure and optically active. The crystal structure of 2-phenylpentaene was determined by X-ray crystallography, which revealed that it has a c-h bond between its two phenyl groups. This bond may have been formed from an interaction with zirconium.Fórmula:C11H15NPureza:Min. 95%Peso molecular:161.24 g/mol3,5-Difluoro-2-methoxyphenylacetic acid
CAS:Versatile small molecule scaffoldFórmula:C9H8F2O3Pureza:Min. 95%Peso molecular:202.16 g/mol3-Methyl-2-(trifluoromethyl)morpholine
CAS:Versatile small molecule scaffoldFórmula:C6H10F3NOPureza:Min. 95%Peso molecular:169.14 g/mol4H,5H,6H,7H-Thieno[3,2-c]pyridine-4-thione
CAS:Versatile small molecule scaffoldFórmula:C7H7NS2Pureza:Min. 95%Peso molecular:169.3 g/mol5-Hydroxy-1-(prop-2-yn-1-yl)piperidin-2-one
CAS:Versatile small molecule scaffoldFórmula:C8H11NO2Pureza:Min. 95%Peso molecular:153.2 g/mol2-Amino-3-fluoro-4-methoxybenzoic acid
CAS:Versatile small molecule scaffoldFórmula:C8H8FNO3Pureza:Min. 95%Peso molecular:185.15 g/mol3-N-Cyclopentylpyridine-2,3-diamine
CAS:Versatile small molecule scaffoldFórmula:C10H15N3Pureza:Min. 95%Peso molecular:177.25 g/mol(5-bromo-3-chloropyridin-2-yl)methanol
CAS:Versatile small molecule scaffoldFórmula:C6H5BrClNOPureza:Min. 95%Peso molecular:222.47 g/mol6-Bromo-4-fluoro-2-methyl-2,3-dihydro-1H-inden-1-one
CAS:Versatile small molecule scaffoldFórmula:C10H8BrFOPureza:Min. 95%Peso molecular:243.07 g/molN-[2-(4-Fluorophenyl)ethyl]-4,5-dihydro-1,3-thiazol-2-amine
CAS:Versatile small molecule scaffoldFórmula:C11H13FN2SPureza:Min. 95%Peso molecular:224.3 g/molEthyl 1-isocyanatocyclobutane-1-carboxylate
CAS:Versatile small molecule scaffoldFórmula:C8H11NO3Pureza:Min. 95%Peso molecular:169.18 g/mol2-[(Prop-2-yn-1-yl)carbamoyl]acetic acid
CAS:Versatile small molecule scaffoldFórmula:C6H7NO3Pureza:Min. 95%Peso molecular:141.12 g/mol4-Morpholinoaniline
CAS:4-Morpholinoaniline is a synthetic substrate that reacts with hydrochloric acid and sodium nitrite to form the reactive intermediate 4-morpholinonitrosobenzene. The reaction mechanism is proposed to proceed through an initial electron transfer from the substrate to the nitrosobenzene intermediate, followed by protonation of the nitrosobenzene nitrogen atom. The resulting 4-nitrophenyl radical abstracts hydrogen from the substrate to give 4-hydroxyphenyl radical. This radical undergoes a nucleophilic attack on the aromatic ring of the substrate molecule, and cleavage of the disulfide bond in the aromatic ring leads to formation of a cyanohydrin product. Studies have been conducted on rat liver microsomes and hepatitis C virus (HCV) to investigate this reaction mechanism.Fórmula:C10H14N2OPureza:Min. 98.5 Area-%Forma y color:Red PowderPeso molecular:178.23 g/mol3-(2-Methoxyphenoxy)pyrrolidine
CAS:Versatile small molecule scaffoldFórmula:C11H15NO2Pureza:Min. 95%Peso molecular:193.24 g/mol2-sec-Butylphenol
CAS:2-sec-Butylphenol is an organic compound that is used as a solvent and has been used in the production of polymers. It can be synthesized from phenol and 2-butanol by cationic polymerization. The reaction mechanism for this process is similar to that of polyethylene, which involves the formation of monomers with reactive double bonds. Aromatase inhibition was observed in a kinetic study of 2-sec-butylphenol with human placental microsomes. This was attributed to the benzene ring substitution at position two on the phenyl group. The genotoxic potential of 2-sec-butylphenol has been investigated by exposing cells to different concentrations and observing DNA damage as measured by comet assay. Solubility data for 2-sec-butylphenol show that it is soluble up to 1g/L in water and up to 1g/L in acetone or ethanol. Low energy is required for polymerFórmula:C10H14OPureza:Min. 95%Peso molecular:150.22 g/mol2,6-Dichlorophenylhydrazine Hydrochloride
CAS:Fórmula:C6H6Cl2N2·HClPureza:>98.0%(T)(HPLC)Forma y color:White to Light yellow to Light orange powder to crystalPeso molecular:213.492-(Aminomethyl)-4-methyl-1,3-thiazole-5-carboxylic acid hydrochloride
CAS:Versatile small molecule scaffoldFórmula:C6H9ClN2O2SPureza:Min. 95%Peso molecular:208.67 g/mol4-[1-(Methoxyimino)ethyl]-2-methylphenol
CAS:Versatile small molecule scaffoldFórmula:C10H13NO2Pureza:Min. 95%Peso molecular:179.22 g/mol
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