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(5.778 prodotti)
- Building Blocks Chirali(1.243 prodotti)
- Building Blocks Idrocarburici(6.097 prodotti)
- Building Blocks organici(61.048 prodotti)
Trovati 203115 prodotti di "Building Blocks"
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2-Bromo-4,5,6,7-tetrahydrothiazolo[4,5-c]pyridine
CAS:<p>2-Bromo-4,5,6,7-tetrahydrothiazolo[4,5-c]pyridine</p>Formula:C6H7BrN2SPurezza:95%Colore e forma:SolidPeso molecolare:219.10g/mol2,3,5,6-Tetrafluoropyridine
CAS:2,3,5,6-TetrafluoropyridineFormula:C5HF4NPurezza:98%Colore e forma: clear. colourless liquidPeso molecolare:151.06g/mol1-(Trifluoroacetyl)piperidin-4-one
CAS:<p>1-(Trifluoroacetyl)piperidin-4-one</p>Purezza:95%Peso molecolare:195.14g/mol1-(2,6-Difluorobenzoyl)piperidin-4-one
CAS:<p>1-(2,6-Difluorobenzoyl)piperidin-4-one</p>Purezza:95+%Peso molecolare:239.22g/molRef: 54-PC446094
Prodotto fuori produzione5-Amino-2-phenyl-2H-1,2,3-triazole-4-carboxamide
CAS:5-Amino-2-phenyl-2H-1,2,3-triazole-4-carboxamidePurezza:≥95%Peso molecolare:203.20g/molRef: 54-OR13277
Prodotto fuori produzioneα-Amino-3-pyridineacetonitrile (>85%)
CAS:Prodotto controllatoFormula:C7H7N3Purezza:>85%Colore e forma:NeatPeso molecolare:133.151Acrolein (stabilized with Hydroquinone)
CAS:Formula:C3H4OColore e forma:Colourless to Pale Yellow OilPeso molecolare:56.062-(4-Methylphenyl)piperidine
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H17NPurezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:175.27 g/molQuinoline 2,4-dicarboxylic acid
CAS:<p>Quinoline 2,4-dicarboxylic acid (QDA) is a novel cytotoxic agent that targets cervical cancer cells. It inhibits the uptake of glucose and other nutrients by cervical cancer cells, leading to cell death through apoptosis. QDA also inhibits the expression of genes involved in cross-linking reactions, which are important for the structural integrity of proteins. This agent has been shown to inhibit the growth of aniline-induced breast cancer cells and glutamate-stimulated PC12 cells. QDA binds to DNA and forms covalent bonds with nucleotide bases, inhibiting DNA synthesis, as well as interfering with protein synthesis and cell division. The QDA mechanism is similar to that of benzoquinolines and estrone sulfate.</p>Formula:C11H7NO4Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:217.18 g/mol5-Butylpyridine-2-carboxamide
CAS:<p>5-Butylpyridine-2-carboxamide is a copper complex that has been shown to inhibit dopamine β-hydroxylase. It is used in clinical studies to measure the effects of dopamine on proximal tubules and pharmaceutical dosage. 5-Butylpyridine-2-carboxamide has a chemical stability that can be measured by picolinic acid. This drug is also used for the diagnosis of polymeric matrix glomerular filtration rate, as well as uv absorption. The hydrogen bonds between the drug and fatty acids are responsible for its cardiac activity.</p>Formula:C10H14N2OPurezza:Min. 95%Colore e forma:PowderPeso molecolare:178.23 g/mol3-Hydroxy-3,4-dihydro-2H-1-benzopyran-4-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H8O3Purezza:Min. 95%Colore e forma:PowderPeso molecolare:164.16 g/mol3,3',5,5'-Tetramethylbenzidine, free base
CAS:<p>Please enquire for more information about 3,3',5,5'-Tetramethylbenzidine, free base including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C16H20N2Purezza:Min. 99.0 Area-%Peso molecolare:240.35 g/mol7-Azaindole
CAS:<p>7-Azaindole is a reactive chemical that has been shown to be effective in the treatment of skin cancer, as well as hepatic steatosis. The compound can promote the transfer of hydrogen atoms and form a dimer with protonated nitrogen. 7-Azaindole reacts rapidly with nucleophiles such as amines, alcohols, and thiols to form covalent bonds. The reaction mechanism is characterized by an initial protonation step followed by nucleophilic attack or hydrogen transfer from the nucleophile to 7-azaindole. Kinetic studies have demonstrated that the rate of this reaction depends on the concentration of both reactants.</p>Formula:C7H6N2Colore e forma:PowderPeso molecolare:118.14 g/mol2,6-Dimethoxy-4-propylphenol
CAS:<p>2,6-Dimethoxy-4-propylphenol is an organic solvent that is used in the synthesis of pharmaceuticals and agricultural chemicals. It is also a precursor for lignin, a natural polymer found in plants. 2,6-Dimethoxy-4-propylphenol can be converted to 2,6-dimethoxyphenol by hydrolysis with water vapor or an acid catalyst. The skeleton of 2,6-dimethoxy-4-propylphenol is a carbon chain with ether linkages that are susceptible to hydrolysis reactions. These reactions produce monomers and fatty acids.</p>Formula:C11H16O3Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:196.24 g/molN-Acetyl-L-alanine
CAS:<p>N-Acetyl-L-alanine is the N-acetylated form of L-alanine and is a nonessential amino acid. It is an amide containing one nitrogen atom and two carbonyl groups. The nitrogen can be found in either the alpha or beta position on the amide. The biological properties of N-acetyl-L-alanine are similar to those of L-alanine, as it is used as a substrate for protein synthesis and has been shown to inhibit p21 and epidermal growth factor. The conformational properties of N-acetyl-L-alanine are different from that of L-alanine due to its changed shape, which may affect its biological activity.</p>Formula:C5H9NO3Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:131.13 g/mol3,3',5,5'-Tetramethylbenzidine, free base
CAS:<p>3,3',5,5'-Tetramethylbenzidine is a high quality chemical that has been used as a research chemical and in the synthesis of other chemicals. It is also used as an intermediate in the synthesis of various building blocks such as benzylidene-p-dioxanone, 3-chloro-2-methylbenzoyl chloride, and 3-phenylpropionitrile. The compound can be used to synthesize a wide range of compounds including pharmaceuticals, pesticides, dyes, and perfumes. It is also useful for the production of drugs such as haloperidol and chloroquine phosphate.</p>Formula:C16H20N2Peso molecolare:240.35 g/mol1,2,3,6-Tetrahydropyridine
CAS:<p>1,2,3,6-Tetrahydropyridine is an experimental drug that acts as a dopamine receptor antagonist. It has been shown to induce neuronal death in the presence of excess dopamine by inhibiting the uptake of dopamine by neurons. The nitrogen atom in position 6 may be involved in binding to the receptor and initiating the conformational change needed for activation. Tetrahydropyridine binds to the D1 and D2 receptors with high affinity, but it does not bind to D4 receptors. Tetrahydropyridine can also inhibit locomotor activity in mice and rats.</p>Formula:C5H9NPurezza:Min. 95%Colore e forma:Colorless Yellow Clear LiquidPeso molecolare:83.13 g/mol5-Hydroxyindole-2-carboxylic acid ethyl ester
CAS:<p>5-Hydroxyindole-2-carboxylic acid ethyl ester is a fluorescent probe that is used in the detection of hepatitis C virus by micropet assay. The compound reacts with amines and undergoes fluorescence quenching, and can be used to quantitate their concentration. 5-Hydroxyindole-2-carboxylic acid ethyl ester is also used for the determination of the kinetics of amines and other compounds that are involved in the metabolism of drugs and biogenic amines. It can be applied to chromatographic analysis or sample preparation prior to analysis by analytical chemistry methods such as gas chromatography or liquid chromatography.</p>Formula:C11H11NO3Purezza:Min. 95%Colore e forma:PowderPeso molecolare:205.21 g/molRef: 3D-FH30383
Prodotto fuori produzione


