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(61.038 prodotti)
Trovati 196817 prodotti di "Building Blocks"
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1-(4-Iodophenyl)ethan-1-ol
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H9IOPurezza:Min. 95%Peso molecolare:248.06 g/mol1-(Pyrimidin-5-yl)propan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H8N2OPurezza:Min. 95%Peso molecolare:136.15 g/mol1,3-Bis(bromomethyl)-5-iodobenzene
CAS:<p>Versatile small molecule scaffold</p>Formula:C8H7Br2IPurezza:Min. 95%Peso molecolare:389.85 g/mol4-(Dibromomethyl)-2(1H)-quinolinone
CAS:<p>Please enquire for more information about 4-(Dibromomethyl)-2(1H)-quinolinone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C10H7Br2NOPurezza:Min. 95%Peso molecolare:316.98 g/mol2,3-Epoxy-1-(1-ethoxyethoxy)propane
CAS:<p>2,3-Epoxy-1-(1-ethoxyethoxy)propane is a water-insoluble solid that has been shown to form stable complexes with metal ions. It is soluble in hydrochloric acid and is polymerized by cationic polymerization. 2,3-Epoxy-1-(1-ethoxyethoxy)propane reacts with the hydroxyl group of polymers to produce epoxides. The epoxide ring can be opened to produce ethers or oxiranes through ring opening reactions. 2,3-Epoxy-1-(1-ethoxyethoxy)propane is an acidic compound and reacts with water vapor to form hydroxy groups. This compound can also be synthesized by transfer reactions from 1,2,4,5-tetrahydrobenzene and ethylene oxide.</p>Formula:C7H14O3Purezza:Min. 95%Peso molecolare:146.18 g/molN-(5-bromo-4-chloro-1H-indol-3-yl)pyrazine-2-carboxamide
<p>Please enquire for more information about N-(5-bromo-4-chloro-1H-indol-3-yl)pyrazine-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C13H8BrClN4OPurezza:Min. 95%Colore e forma:PowderPeso molecolare:351.59 g/mol4-[(1,1-Dimethylethoxy)carbonyl]-2-thiomorpholineacetic acid
CAS:<p>Please enquire for more information about 4-[(1,1-Dimethylethoxy)carbonyl]-2-thiomorpholineacetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C11H19NO4SPurezza:Min. 95%Peso molecolare:261.34 g/mol2,6-Di-tert-butyl-4-(morpholinomethyl)phenol
CAS:<p>Please enquire for more information about 2,6-Di-tert-butyl-4-(morpholinomethyl)phenol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C19H31NO2Purezza:Min. 95%Peso molecolare:305.46 g/mol6-Bromo-3-methyl-3H-imidazo[4,5-c]pyridine
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H6BrN3Purezza:Min. 95%Peso molecolare:212.05 g/mol1H-Pyrrole-2,3,4,5-tetracarboxylic acid
CAS:<p>Please enquire for more information about 1H-Pyrrole-2,3,4,5-tetracarboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C8H5NO8Purezza:Min. 95%Peso molecolare:243.13 g/mol1,1-Dimethylethyl 4-[3-[[4-[[[2-[(2S)-2-cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]amino]carbonyl]-6-quinolinyl]methylamino]propy l]-1-piperazinecarboxylate
CAS:<p>Please enquire for more information about 1,1-Dimethylethyl 4-[3-[[4-[[[2-[(2S)-2-cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]amino]carbonyl]-6-quinolinyl]methylamino]propy l]-1-piperazinecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C30H39F2N7O4Purezza:Min. 95%Peso molecolare:599.67 g/mol2-(2,6-Dimethylpyridin-3-yl)propan-2-amine
CAS:<p>Please enquire for more information about 2-(2,6-Dimethylpyridin-3-yl)propan-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C10H16N2Purezza:Min. 95%Peso molecolare:164.25 g/mol5-Fluoro-UTP trisodium
CAS:<p>Please enquire for more information about 5-Fluoro-UTP trisodium including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C9H14FN2O15P3•Na3Purezza:Min. 95%Peso molecolare:571.1 g/molFmoc-2,6-dichloro-L-phenylalanine
CAS:<p>Please enquire for more information about Fmoc-2,6-dichloro-L-phenylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C24H19Cl2NO4Purezza:Min. 95%Peso molecolare:456.32 g/mol2-Cyclopentyl-2-oxoacetic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H10O3Purezza:Min. 95%Peso molecolare:142.15 g/molPiperyline
CAS:<p>Piperyline is an alkanoic acid that has shown to be effective against skin cancer. It also has antimicrobial properties, which may be due to its ability to bind metal ions and form polymeric compounds. Piperyline inhibits microbial growth by inhibiting the synthesis of proteins and nucleic acids. The antimicrobial activity is related to its cationic polymerization with hydroxyl groups, which forms a structure that can inhibit microbial enzymes and disrupt microbial cell membranes. This compound also interacts with the skin's natural lipids, making it difficult for microorganisms to attach and grow on the skin. Piperyline is synthesized in organic chemistry laboratories as an amide precursor of other pharmaceuticals such as penicillin.</p>Formula:C16H17NO3Purezza:Min. 95%Peso molecolare:271.31 g/molD-Carnosine
CAS:<p>Please enquire for more information about D-Carnosine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C9H14N4O3Purezza:Min. 95%Peso molecolare:226.23 g/molCarbamic acid (R)-1-(2-chlorophenyl)-2-(1H-tetrazol-1-yl)ethyl ester
CAS:<p>Please enquire for more information about Carbamic acid (R)-1-(2-chlorophenyl)-2-(1H-tetrazol-1-yl)ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C10H10ClN5O2Purezza:Min. 95%Peso molecolare:267.67 g/molDebacarb
CAS:<p>Debacarb is a subtilis mutant strain that produces the active substances debacarb and debacin. Debacarb inhibits the mitochondrial cytochrome b-245, which is an enzyme in the electron transport chain of mitochondria. It also inhibits bacterial growth by binding to nicotinic acetylcholine, which is an enzyme involved in the synthesis of bacterial cell walls. The target enzymes for this compound are not yet known. The bacterium Agrobacterium tumefaciens was found to be sensitive to Debacarb, but resistant strains were also obtained. Debacarb has been used as an agrochemical against bacterial strains such as Pseudomonas syringae and Erwinia carotovora. The effective dose for Debacarb varies depending on the bacterial strain. The most common effective doses are between 2 and 5 ppm, but higher concentrations may be needed against some bacteria.br> Debacarb can inhibit polymerase chain reactions, which</p>Formula:C14H19N3O4Purezza:Min. 95%Peso molecolare:293.32 g/mol5-Methyl-1-(piperidin-4-yl)-1H-pyrazole-4-carboxylic acid dihydrochloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C10H17Cl2N3O2Purezza:Min. 95%Peso molecolare:282.16 g/mol
