Building Blocks
Questa sezione contiene prodotti fondamentali per la sintesi di composti organici e biologici. Building blocks sono i materiali di partenza essenziali utilizzati per costruire molecole complesse attraverso varie reazioni chimiche. Svolgono un ruolo critico nella scoperta di farmaci, nella scienza dei materiali e nella ricerca chimica. Presso CymitQuimica, offriamo una gamma diversificata di building blocks di alta qualità per supportare le tue ricerche innovative e progetti industriali, assicurandoti di avere i componenti essenziali per una sintesi di successo.
Sottocategorie di "Building Blocks"
- Acidi boronici e derivati dell'acido boronico(5.756 prodotti)
- Building Blocks Chirali(1.242 prodotti)
- Building Blocks Idrocarburici(6.095 prodotti)
- Building Blocks organici(61.051 prodotti)
Trovati 199813 prodotti di "Building Blocks"
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6-Bromo-2-oxo-2,3-dihydro-1H-indole-3-carbaldehyde
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H6BrNO2Purezza:Min. 95%Peso molecolare:240.05 g/mol1-(3-tert-Butyl-1,2,4-oxadiazol-5-yl)cyclohexan-1-amine hydrochloride
CAS:Prodotto controllato<p>Versatile small molecule scaffold</p>Formula:C12H22ClN3OPurezza:Min. 95%Peso molecolare:259.77 g/mol2-Chloro-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H13ClN2O3Purezza:Min. 95%Peso molecolare:256.68 g/mol2,6-Dichloro-N'-hydroxybenzene-1-carboximidamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H6Cl2N2OPurezza:Min. 95%Peso molecolare:205.04 g/molN-Methyl-4-phenoxyaniline
CAS:<p>N-Methyl-4-phenoxyaniline is a molecule that inhibits chitinase, an enzyme that catalyzes the hydrolysis of chitin, and molting. N-Methyl-4-phenoxyaniline has been shown to be potent inhibitor of the enzyme amide in vitro. It also inhibits onchocerca volvulus and in vivo, which may be due to its ability to inhibit the synthesis of fatty acids. This drug has not been tested against other parasites or mammals, but it is an anthelmintic drug.</p>Formula:C13H13NOPurezza:Min. 95%Peso molecolare:199.25 g/mol2-(2-Phenoxyacetamido)propanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H13NO4Purezza:Min. 95%Peso molecolare:223.22 g/molMethyl 4-(4-bromo-2-fluorophenoxy)butanoate
CAS:Prodotto controllato<p>Versatile small molecule scaffold</p>Formula:C11H12BrFO3Purezza:Min. 95%Peso molecolare:291.11 g/mol3-{[3-(Trifluoromethyl)-1H-pyrazol-1-yl]methyl}benzoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H9F3N2O2Purezza:Min. 95%Peso molecolare:270.21 g/mol4-bromo-1-hydroxynaphthalene-2-carboxylic acid
CAS:<p>4-Bromo-1-hydroxynaphthalene-2-carboxylic acid (4BHN) is a spectroscopic compound that has been used as a radioligand to study the binding of dopamine and dopamine D3 receptors. This compound binds to the d3 receptor with high affinity and specificity, but it does not interact with the d1 or d2 receptors. 4BHN has been shown to act as an agonist at the dopamine D3 receptor. It also acts as an antagonist at the piperidine site of the dopamine D2 receptor. The effects of 4BHN are reversible, which means that it can be displaced by unlabeled 4BHN or other compounds that bind to the same site on the receptor. This technique is useful for studying drug interactions and for determining whether drugs have a subtype selectivity profile.</p>Formula:C11H7BrO3Purezza:Min. 95%Peso molecolare:267.1 g/mol5-(1-Methylcyclopropyl)-1,2-oxazol-3-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H10N2OPurezza:Min. 95%Peso molecolare:138.17 g/mol1-(2,2-Dimethylcyclopropyl)butan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H16OPurezza:Min. 95%Peso molecolare:140.22 g/mol2-Bromo-3,3,3-trifluoro-1-propene
CAS:Prodotto controllato<p>2-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%.</p>Formula:C3H2BrF3Purezza:Min. 95%Colore e forma:Colorless PowderPeso molecolare:174.95 g/mol3-Boc-3-azabicyclo[3.2.1]octan-8-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H22N2O2Purezza:Min. 95%Peso molecolare:226.32 g/mol
![2-Chloro-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethan-1-one](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FEEB57887.webp&w=3840&q=75)
![3-{[3-(Trifluoromethyl)-1H-pyrazol-1-yl]methyl}benzoic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FEQB64362.webp&w=3840&q=75)
![3-Boc-3-azabicyclo[3.2.1]octan-8-amine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FFDC76351.webp&w=3840&q=75)