Building Blocks
Cette section contient des produits fondamentaux pour la synthèse de composés organiques et biologiques. Building blocks sont les matériaux de départ essentiels utilisés pour construire des molécules complexes à travers diverses réactions chimiques. Ils jouent un rôle crucial dans la découverte de médicaments, la science des matériaux et la recherche chimique. Chez CymitQuimica, nous offrons une gamme diversifiée de building blocks de haute qualité pour soutenir vos recherches innovantes et projets industriels, en vous assurant de disposer des composants essentiels pour une synthèse réussie.
Sous-catégories appartenant à la catégorie "Building Blocks"
- Acides boroniques et dérivés de l'acide boronique(5.780 produits)
- Building Blocks Chiraux(1.241 produits)
- Building Blocks Hydrocarbonés(6.100 produits)
- Building Blocks organiques(61.024 produits)
205297 produits trouvés pour "Building Blocks"
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(Tetrahydro-pyran-2-yl)-acetic acid
CAS :Tetrahydro-pyran-2-yl)-acetic acid is an unsaturated acetic acid that can be synthesized by esters of tetrahydro-pyran-2-yl)acetic acid. Tetrahydro-pyran-2-yl)-acetic acid is produced by the catalyzed cyclization of ethyl acetoacetate and pivalic acid chloride. The heptahydrate form has been shown to undergo hydrolysis in aqueous solution to produce the monohydrated form, which is soluble in water. This compound has been shown to react with benzene, acetone, and ethyl acetoacetate in the presence of a Lewis acid catalyst to form substituted tetrahydropyrans.Formule :C7H12O3Degré de pureté :Min. 95%Masse moléculaire :144.17 g/mol1-(3-Hydroxyphenyl)-1-propanone
CAS :1-(3-Hydroxyphenyl)-1-propanone is a monocyclic compound that has been shown to have antioxidative activity, which may be due to its ability to inhibit the formation of reactive oxygen species. It has been shown to be effective against E. coli cells and benzene degradation, as well as other dehydrogenases such as butyrophenone and trifluoroacetophenone. 1-(3-Hydroxyphenyl)-1-propanone also inhibits e. coli growth by acting on the propiophenone pathway (involving conversion of phenylalanine into propiophenone). The escherichia bacterium can convert 1-(3-hydroxyphenyl)-1-propanone into the vicinal diol, 2,2-diphenyldi(3H)oxazole.Formule :C9H10O2Degré de pureté :Min. 95%Masse moléculaire :150.17 g/mol4-Chloro-3,3-dimethylbutan-2-one
CAS :Versatile small molecule scaffold
Formule :C6H11ClODegré de pureté :Min. 95%Masse moléculaire :134.6 g/mol2-(4-Aminophenyl)-2-hydroxyacetic acid
CAS :Versatile small molecule scaffoldFormule :C8H9NO3Degré de pureté :Min. 95%Masse moléculaire :167.16 g/mol2-(4-Methylphenyl)oxirane
CAS :2-(4-Methylphenyl)oxirane (2MPO) is an epoxide that belongs to the group of reactive compounds. It has been shown to react with nucleic acids, forming a covalent linkage with guanosine. 2MPO also reacts with styrene, forming a covalent bond and producing reactive metabolites. The reaction products are hydroxylated by hydroxyl groups on the ring structure, which catalyzes the reaction. Additives can be used to alter the rate of this reaction. 2MPO is also known to react with pluronic F127, forming a covalently linked adduct. This bond is cleaved by hydrolysis in water and exposure to light, releasing 2MPO and regenerating pluronic F127.Formule :C9H10ODegré de pureté :Min. 95%Masse moléculaire :134.17 g/mol2-(3-Methyl-4H-1,2,4-triazol-4-yl)aniline
CAS :Versatile small molecule scaffoldFormule :C9H10N4Degré de pureté :Min. 95%Masse moléculaire :174.2 g/mol(2S)-2-Hydroxy-2-phenylpropanoic acid
CAS :(2S)-2-Hydroxy-2-phenylpropanoic acid is a chiral compound that can be synthesized from the corresponding racemic mixture. The structure of (2S)-2-hydroxy-2-phenylpropanoic acid was elucidated by x-ray crystallography, revealing an asymmetric dimaleate. The molecule shows anti-inflammatory and analgesic effects in rats, which are likely due to its inhibition of prostaglandin synthesis.Formule :C9H10O3Degré de pureté :Min. 95%Masse moléculaire :166.17 g/mol(Pyridin-3-yl)urea
CAS :(Pyridin-3-yl)urea is a coordination compound that has a molecular formula of C5H5N. It has the ability to form hydrogen bonds with other molecules. The compound belongs to the class of supramolecular compounds, which are made up of more than one type of molecule. (Pyridin-3-yl)urea can form hydrogen bonds with sulfate salts and assemble into a supramolecular complex with water molecules. This complex is able to encapsulate sulfate ions, forming tripodal structures. These tripodal structures can be used as an alternative to standard methods for the removal of sulfates from wastewater.Formule :C6H7N3ODegré de pureté :Min. 95%Masse moléculaire :137.14 g/molN-(2,3-Dimethylphenyl)urea
CAS :Versatile small molecule scaffoldFormule :C9H12N2ODegré de pureté :Min. 95%Masse moléculaire :164.2 g/molN-(2-Cyanophenyl)-nprime-phenylurea
CAS :Versatile small molecule scaffoldFormule :C14H11N3ODegré de pureté :Min. 95%Masse moléculaire :237.26 g/molEthyl 2-oxo-3-(quinolin-2-yl)propanoate
CAS :Versatile small molecule scaffold
Formule :C14H13NO3Degré de pureté :Min. 95%Masse moléculaire :243.26 g/molEthyl 2,3-dicyano-3-methylpropanoate
CAS :Versatile small molecule scaffoldFormule :C8H10N2O2Degré de pureté :Min. 95%Masse moléculaire :166.18 g/mol1-(3,4-Dichlorophenyl)-3-methyl-4,5-dihydro-1H-pyrazol-5-one
CAS :Versatile small molecule scaffoldFormule :C10H8Cl2N2ODegré de pureté :Min. 95%Masse moléculaire :243.09 g/mol3-Methoxy-1-phenylpropan-1-ol
CAS :3-Methoxy-1-phenylpropan-1-ol is a colorless liquid with a fruity odor. It is used in the synthesis of organic compounds and as an intermediate for other organic syntheses. 3-Methoxy-1-phenylpropan-1-ol is a precursor to methoxyphenols, which are used in the manufacture of pesticides, pharmaceuticals and dyes. Methoxyphenols are also precursors to phenolic resins, which are used as binders for paints and coatings. 3-Methoxypropane can be prepared by electrolysis of methanol or by carbonate hydrolysis of methyl acetate in the presence of sodium methoxide. The methanol reacts with sodium methoxide to form methyl acetate and methanolic hydrochloric acid.Formule :C10H14O2Degré de pureté :Min. 95%Masse moléculaire :166.22 g/mol3-Thietanecarboxylicacid,1,1-dioxide
CAS :Versatile small molecule scaffoldFormule :C4H6O4SDegré de pureté :Min. 95%Masse moléculaire :150.15 g/mol2-(Acetylamino)-4,5-dimethylthiophene-3-carboxylic acid
CAS :Versatile small molecule scaffoldFormule :C9H11NO3SDegré de pureté :Min. 95%Masse moléculaire :213.25 g/mol5-Methyl-4-oxa-8-thia-6-azatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),5-trien-3-one
CAS :Versatile small molecule scaffoldFormule :C11H11NO2SDegré de pureté :Min. 95%Masse moléculaire :221.28 g/mol1-Bromoisoquinolin-3-amine
CAS :1-Bromoisoquinolin-3-amine is a naphthyridine that can be synthesized by the reaction of 1-chloroisonicotinic acid with sodium azide and bromine. This compound has the potential to be used for the synthesis of other compounds, such as thiazolopyrimidines and benzothiazoles. Irradiation of 1-Bromoisoquinolin-3-amine in a nitrogen atmosphere yields an isomer with a phosphite group at C2. The tricycle structure of this isomer makes it reactive towards nucleophilic substitution reactions, making it useful for synthetic purposes.Formule :C9H7BrN2Degré de pureté :Min. 95%Masse moléculaire :223.07 g/molN-Phenylpyrazin-2-amine
CAS :N-Phenylpyrazin-2-amine is a tetrazole that has been shown to have an axial configuration. It is also a polymorph of the molecule, which means it can exist in different crystalline structures. N-Phenylpyrazin-2-amine has been shown to form hydrogen bonds with chlorine and hydrogen bonds with benzotriazole. The nitrogen atom in this compound is bonded to two phenyltetrazole rings and one carbon atom. This chain crystal structure was found to be monoclinic in nature.
Formule :C10H9N3Degré de pureté :Min. 95%Masse moléculaire :171.2 g/molMethyl 3-hydroxybenzo[b]thiophene-2-carboxylate
CAS :Methyl 3-hydroxybenzo[b]thiophene-2-carboxylate is an intermediate in the synthesis of nitrobenzene. It is also a synthon for benzothiophene esters and functionalized derivatives.
Formule :C10H8O3SDegré de pureté :Min. 95%Masse moléculaire :208.23 g/mol
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