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
- Building Blocks Chirali
- Building Blocks Idrocarburici
- Building Blocks organici
Prodotti di "Building Blocks"
Ordinare per
3-Bromo-2-(cyclopentyloxy)pyridine
CAS:Versatile small molecule scaffoldFormula:C10H12BrNOPurezza:Min. 95%Peso molecolare:242.11 g/mol1-[4-(2-Methoxyethoxy)phenyl]ethan-1-one
CAS:Versatile small molecule scaffoldFormula:C11H14O3Purezza:Min. 95%Peso molecolare:194.23 g/mol2-(azetidin-3-yl)-7-Methyl-[1,2,4]triazolo[5,1-f]pyridin-5-ol
CAS:Please enquire for more information about 2-(azetidin-3-yl)-7-Methyl-[1,2,4]triazolo[5,1-f]pyridin-5-ol including the price, delivery time and more detailed product information at the technical inquiry form on this pagePurezza:Min. 95%(2-Cyclobutoxypyridin-4-yl)methanamine
CAS:Versatile small molecule scaffoldFormula:C10H14N2OPurezza:Min. 95%Peso molecolare:178.23 g/molS-Propyl Thioacetate
CAS:Formula:C5H10OSPurezza:>98.0%(GC)Colore e forma:Colorless to Light yellow clear liquidPeso molecolare:118.193-(4-Acetylphenyl)-1,2,3λ⁵-oxadiazol-3-ylium-5-olate
CAS:3-(4-Acetylphenyl)-1,2,3λ⁵-oxadiazol-3-ylium-5-olate is an antibacterial agent that reacts with thioacetamide to form a reactive intermediate. The reactant then undergoes a 1,3-dipolar cycloaddition with the azide group on the DNA of gram-negative bacteria. 3-(4-Acetylphenyl)-1,2,3λ⁵-oxadiazol-3-ylium-5-olate inhibits growth of organisms by acting as a competitive inhibitor rather than as an enzyme inhibitor. It has been shown to be effective against both gram negative and gram positive bacteria, but not fungi or viruses.Formula:C10H8N2O3Purezza:Min. 95%Peso molecolare:204.18 g/mol(2-Aminoethyl)(ethyl)(2-ethylbutyl)amine dihydrochloride
CAS:Versatile small molecule scaffoldFormula:C10H26Cl2N2Purezza:Min. 95%Peso molecolare:245.23 g/molN-(2-Aminoethyl)-2-cyclopentylacetamide
CAS:Versatile small molecule scaffoldFormula:C9H18N2OPurezza:Min. 95%Peso molecolare:170.25 g/mol2-Ethyl-1-hexanol
CAS:Formula:C8H18OPurezza:>99.5%(GC)Colore e forma:Colorless clear liquidPeso molecolare:130.23Lazabemide hydrochloride
CAS:Lazabemide hydrochloride is a drug that inhibits the action of monoamine oxidase (MAO) in the body. It is used to treat bowel disease, such as ulcerative colitis and Crohn's disease. Lazabemide hydrochloride has been shown to be a potent inhibitor of MAO-A and MAO-B and can be detected in maternal blood samples. Lazabemide hydrochloride inhibits the metabolism of monoamines, including serotonin and dopamine, which are neurotransmitters that regulate mood, appetite, sleep patterns, and sexual function. Lazabemide hydrochloride also has genotoxic activity in vitro and can cause mutations in DNA. This drug may interact with other drugs by inhibiting their action.Formula:C8H10ClN3O·HClPurezza:Min. 95%Peso molecolare:236.1 g/mol2-{[4-(tert-Butoxycarbonyl)piperazin-1-yl]carbonyl}cyclopropane-1-carboxylic acid
CAS:2-{[4-(tert-Butoxycarbonyl)piperazin-1-yl]carbonyl}cyclopropane-1-carboxylic acidPeso molecolare:298.33g/mol6-Oxa-2-azaspiro[3.4]octane HCl
CAS:Versatile small molecule scaffoldFormula:C6H12ClNOPurezza:Min. 95%Peso molecolare:149.62 g/mol4-Oxooxane-2-carboxylic acid
CAS:4-Oxooxane-2-carboxylic acid is a molecule that is involved in the stabilization of organic compounds. It is also used as a reaction rate catalyst for the ring-opening of orotic acid. 4-Oxooxane-2-carboxylic acid can stabilize carbanions and zwitterions, which are reactive intermediates in organic reactions. The mechanism of 4-Oxooxane-2-carboxylic acid's activity involves nucleophilic attack on the carbonyl carbon atom, leading to decarboxylation and formation of the corresponding carboxylate anion. This model system can be used to study nucleophilic reactions.Formula:C6H8O4Purezza:Min. 95%Peso molecolare:144.12 g/mol1-(3-Thienylmethyl)piperazine
CAS:Versatile small molecule scaffoldFormula:C9H14N2SPurezza:Min. 95%Peso molecolare:182.29 g/molEthyl 6,7-dichloro-3-hydroxyquinoxaline-2-carboxylate
CAS:Ethyl 6,7-dichloro-3-hydroxyquinoxaline-2-carboxylatePeso molecolare:287.10g/mol1,3-DIMETHYL-1H-THIENO[2,3-C]PYRAZOLE-5-CARBOXYLIC ACID
CAS:Formula:C8H8N2O2SPurezza:95%Colore e forma:SolidPeso molecolare:196.22634-Oxa-7λ⁶-thia-1-azabicyclo[3.2.1]octane-7,7-dione
CAS:Versatile small molecule scaffoldFormula:C5H9NO3SPurezza:Min. 95%Peso molecolare:163.2 g/mol4-(Azetidin-3-yloxy)-1-cyclopropyl-6-methylpyridin-2(1H)-one hydrochloride
CAS:Versatile small molecule scaffoldFormula:C12H17ClN2O2Purezza:Min. 95%Peso molecolare:256.73 g/mol3-Neopentylisoxazol-5-amine
CAS:Versatile small molecule scaffoldFormula:C8H14N2OPurezza:Min. 95%Peso molecolare:154.21 g/mol
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