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(6.099 prodotti)
- Building Blocks organici(61.038 prodotti)
Trovati 205376 prodotti di "Building Blocks"
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Dibromoethane-d4
CAS:Prodotto controllatoPlease enquire for more information about Dibromoethane-d4 including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C2H4Br2Purezza:Min. 95%Peso molecolare:191.89 g/mol3-Bromo-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazine-5-carboxylic acid tert-butyl ester
CAS:Versatile small molecule scaffold
Formula:C11H16BrN3O2Purezza:Min. 95%Peso molecolare:302.17 g/mol2-Bromocyclopentanone
CAS:2-Bromocyclopentanone is an organic molecule that is used in the synthesis of epoxides. It is also a potential precursor for the synthesis of polymers, dyes, and pharmaceuticals. 2-Bromocyclopentanone has been shown to undergo photolysis when irradiated with ultraviolet light or through chemical reaction with acetonitrile. This product has two conformers with different rotational barriers and corresponding spectral properties. The two conformers can be distinguished by their ultraviolet spectra. The synthetic methods for 2-bromocyclopentanone involve halogenation followed by hydrolysis to yield bromoacetic acid, which is then converted to the desired product by acylation or alkylation.
Formula:C5H7BrOPurezza:Min. 95%Peso molecolare:163.01 g/mol(4R)-5,7-Difluoro-3,4-dihydro-2H-1-benzopyran-4-ol
CAS:Versatile small molecule scaffoldFormula:C9H8F2O2Purezza:Min. 95%Peso molecolare:186.15 g/mol1-(piperazin-1-yl)butan-1-one
CAS:1-(Piperazin-1-yl)butan-1-one is a neoplastic cell growth inhibitor that inhibits the proliferation of myeloid, k562 and HL60 cells. It has been shown to inhibit the growth of tumor cells in vitro. 1-(Piperazin-1-yl)butan-1-one is an analog of piperazine, which is known to be a cytotoxic agent with anticancer activity. The mechanism of action is not known, but it may be due to its ability to inhibit DNA synthesis or its inhibition of protein synthesis.Formula:C8H16N2OPurezza:Min. 95%Peso molecolare:156.23 g/molMethyl 2-(6-chloropyridin-3-yl)acetate
CAS:Versatile small molecule scaffold
Formula:C8H8ClNO2Purezza:Min. 95%Peso molecolare:185.61 g/mol1-(3,5-Dichloro-phenyl)-propan-1-one
CAS:Versatile small molecule scaffold
Formula:C9H8Cl2OPurezza:Min. 95%Peso molecolare:203.07 g/mol(R)-2-(Methoxymethyl)-morpholine hydrochloride
CAS:Versatile small molecule scaffoldFormula:C6H14ClNO2Purezza:Min. 95%Peso molecolare:167.63 g/molMethyl amino(2-chlorophenyl)acetate hydrochloride
CAS:Versatile small molecule scaffoldFormula:C9H11Cl2NO2Purezza:Min. 95%Peso molecolare:236.1 g/mol6,6-difluoro-1,4-oxazepane hydrochloride
CAS:Versatile small molecule scaffoldFormula:C5H10ClF2NOPurezza:Min. 95%Peso molecolare:173.6 g/mol(2S)-3-Hydroxy-2-phenylpropanoic acid
CAS:(2S)-3-Hydroxy-2-phenylpropanoic acid is an unlabelled, naturally occurring compound. It is the citric acid analog of L-phenylalanine. The structure of (2S)-3-Hydroxy-2-phenylpropanoic acid is a skeleton that consists of one hydroxyl group and one carboxylic acid group. The carboxylic acid group has a double bond in the alpha position to the carboxyl carbon, which gives this molecule an acidic character. The chloride ion is also present in this structure. This molecule can be synthesized by a kinetic reaction that involves fatty acids and brugmansia as catalysts. It can also be synthesized through a catalysed reaction using thionyl chloride as a catalyst.Formula:C9H10O3Purezza:Min. 95%Peso molecolare:166.17 g/mol2-Hydroxy-3-(1-methylethyl)-butanedioic acid
CAS:2-Hydroxy-3-(1-methylethyl)-butanedioic acid is an organic compound that is a metabolite of the amino acid methionine. It is formed by the oxidation of the methyl group on the 2 position in methionine. The protein subunits are expressed in liver cells and it has been shown to have antioxidant properties. The analytical methods used for this compound include LC-MS/MS, which separates it into its individual isomers. This method can be used to determine the purity of 2-hydroxy-3-(1-methylethyl)-butanedioic acid. The carbonyl group in this molecule makes it susceptible to steric interactions with other molecules, which may lead to it being oxidized or reduced. It has been found that 2-hydroxy-3-(1-methylethyl)-butanedioic acid shows thermophilic and enterocolitic properties.Formula:C7H12O5Purezza:Min. 95%Peso molecolare:176.17 g/mol5-bromo-3-methoxy-1h-pyrazole
CAS:Versatile small molecule scaffoldFormula:C4H5BrN2OPurezza:Min. 95%Peso molecolare:177 g/mol(1S,3R,4R)-3-(Boc-amino)-4-hydroxy-cyclohexanecarboxylic acid ethyl ester
CAS:Versatile small molecule scaffold
Formula:C14H25NO5Purezza:Min. 95%Peso molecolare:287.35 g/mol2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]-benzonitrile
CAS:2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]-benzonitrile is an antibacterial agent that belongs to the group of nitro compounds. It inhibits bacterial growth by blocking the synthesis of proteins and DNA. 2-[(6-Chloro-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl)methyl]-benzonitrile has been shown to be active against a wide range of bacteria including Gram positive and Gram negative organisms. This compound also exhibits metal ion chelating properties and can be used for the removal of heavy metals from water. The square planar geometry of 2-[(6-Chloro-3,4-(dihydro)-3-(methyl)-2,4-(dioxo)-1Formula:C13H10ClN3O2Purezza:Min. 95%Peso molecolare:275.69 g/mol3-(4-Hydroxyphenyl)hex-4-ynoic acid
CAS:Versatile small molecule scaffoldFormula:C12H12O3Purezza:Min. 95%Peso molecolare:204.22 g/molThiophen-3-ylmethanamine hydrochloride
CAS:Versatile small molecule scaffold
Formula:C5H8ClNSPurezza:Min. 95%Peso molecolare:149.64 g/mol5-(3-Hydroxyphenyl)-1H-pyrazole-3-carboxylic acid
CAS:Versatile small molecule scaffold
Formula:C10H8N2O3Purezza:Min. 95%Peso molecolare:204.18 g/mol2-(2,4-dimethoxyphenyl)ethan-1-amine
CAS:Prodotto controllatoVersatile small molecule scaffoldFormula:C10H15NO2Purezza:Min. 95%Peso molecolare:181.24 g/mol5-Chloro-2-ethoxy-phenylamine
CAS:5-Chloro-2-ethoxy-phenylamine is an enzyme inhibitor that binds to the active site of glucocerebrosidase, the enzyme that catalyzes the hydrolysis of glucocerebroside to glucose and ceramide. This compound has been shown to be a selective inhibitor against this enzyme and not affect other hydrolases or chaperones. It was also found that 5-chloro-2-ethoxy-phenylamine can act as a chemical chaperone by stabilizing protein folding in vitro. 5-Chloro-2-ethoxy phenylamine is a new analogue of 3-(3,4,-dichlorophenyl)-1-[(1R,2S)-2-(5,6,-dichloropyridin-3 yl)ethenyl]-1H-pyrazole. It is an inhibitor of Gaucher disease caused by gluFormula:C8H10ClNOPurezza:Min. 95%Peso molecolare:171.63 g/mol
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