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(6.093 prodotti)
- Building Blocks organici(60.522 prodotti)
Trovati 195533 prodotti di "Building Blocks"
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2-Chloro-4-mercaptobenzonitrile
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H4ClNSPurezza:Min. 95%Peso molecolare:169.6 g/molMethyl-2-benzyl-5-methyl-octahydro-1H-pyrrolo[3,4-c]pyridine-7a-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C17H24N2O2Purezza:Min. 95%Peso molecolare:288.4 g/mol[2-(Piperidin-1-yl)pyridin-3-yl]methanamine dihydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H19Cl2N3Purezza:Min. 95%Peso molecolare:264.19 g/molNaphthalene-2-carboximidamide
CAS:<p>Naphthalene-2-carboximidamide is a benzamidine derivative that interacts with the active site of serine proteases. It was shown to have potent inhibitory potency against a number of proteinases, including urokinase-type plasminogen activator (uPA), matrix metalloproteinase-9 (MMP-9), and cathepsin G. The interaction of naphthalene-2-carboximidamide with uPA was specific and led to inhibition of its catalytic activity. Naphthalene-2-carboximidamide has been tested in clinical trials for the treatment of influenza.</p>Formula:C11H10N2Purezza:Min. 95%Peso molecolare:170.21 g/mol2-(Oxan-4-yl)butanoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H16O3Purezza:Min. 95%Peso molecolare:172.22 g/molMethyl 5-hydrazinyl-2-methylbenzoate dihydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H14Cl2N2O2Purezza:Min. 95%Peso molecolare:253.12 g/mol(1-Bromocyclopentyl)(phenyl)methanone
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13BrOPurezza:Min. 95%Peso molecolare:253.13 g/mol2-Isocyanato-1-methoxybutane
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H11NO2Purezza:Min. 95%Peso molecolare:129.2 g/mol2-Cyclopropylbenzaldehyde
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H10OPurezza:Min. 95%Peso molecolare:146.19 g/mol(4-Methyl-2-piperazinyl)methanol
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H14N2OPurezza:Min. 95%Peso molecolare:130.19 g/mol1-(2-Methylpyrimidin-4-yl)ethan-1-amine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H11N3Purezza:Min. 95%Peso molecolare:137.18 g/mol2-Cyano-5-fluorophenol
CAS:<p>2-Cyano-5-fluorophenol is an organic compound that is used as a precursor to medicines and other chemicals. It reacts with calcium hydroxide in water to form 2-cyano-5-hydroxyfluorobenzene, which can be hydrolyzed to form 2-cyano-5-chlorofluorobenzene. This compound can also react with sodium hydroxide to produce sodium cyanate, which can be hydrolyzed to form sodium chloride and hydrogen cyanide gas. The alkali metal ions are needed for this reaction, which is why the product should not be exposed to water or moisture. 2-Cyano-5-fluorophenol has been shown to have liquid crystal properties and is used in the production of certain types of polymers. 2Cyano-5Fluorophenol crystals are also used in some medicines such as acetaminophen (paracetamol).</p>Formula:C7H4FNOPurezza:Min. 95%Peso molecolare:137.11 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/mol
![Methyl-2-benzyl-5-methyl-octahydro-1H-pyrrolo[3,4-c]pyridine-7a-carboxylate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FVXC57025.webp&w=3840&q=75)
![[2-(Piperidin-1-yl)pyridin-3-yl]methanamine dihydrochloride](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FFDD50657.webp&w=3840&q=75)
