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.
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- Acidi boronici e derivati dell'acido boronico(5.778 prodotti)
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1-(Hydroxymethyl)azepan-2-one
CAS:1-(Hydroxymethyl)azepan-2-one is a lactam. It is a monomer that can be used in the production of polymers such as polystyrene and polyvinyl chloride. 1-(Hydroxymethyl)azepan-2-one is soluble in organic solvents and has a high viscosity, which makes it useful for its interaction with other chemicals. 1-(Hydroxymethyl)azepan-2-one reacts with ethylene to form styrene, which is a condensation product. It can also react with hydrochloric acid to form an acid catalyst. The reaction products of this chemical are styrene, phenolic compounds, and ammonium salts.Formula:C7H13NO2Purezza:Min. 95%Peso molecolare:143.18 g/mol(2R)-2-Hydroxypentanedioic acid
CAS:(2R)-2-Hydroxypentanedioic acid is a metabolite of 2-hydroxyglutarate that is produced in the metabolism of glucose. This compound has been shown to be elevated in gliomas and may serve as a diagnostic marker for this type of cancer. A mutation in isocitrate dehydrogenase, an enzyme that catalyzes the conversion of isocitrate to alpha-ketoglurate, has been shown to be associated with gliomas. This mutation leads to accumulation of (2R)-2-hydroxypentanedioic acid and increases the risk for this type of cancer. The elevated levels of (2R)-2-hydroxypentanedioic acid can be used as a biomarker for disease activity and diagnosis.Formula:C5H8O5Purezza:Min. 95%Peso molecolare:148.11 g/molN-(4-Oxo-2-thioxo-thiazolidin-3-yl)-benzamide
CAS:Versatile small molecule scaffoldFormula:C10H8N2O2S2Purezza:Min. 95%Peso molecolare:252.3 g/molN-{[(2-Chlorophenyl)methylidene]amino}guanidine
CAS:Guanidine is a molecule that contains a guanidinium group. It has cytotoxic effects on cancer cells and the ability to inhibit influenza virus proliferation. Guanidine also inhibits protein phosphatase activity, which may be due to its ability to dephosphorylate proteins. This drug can cause neuronal death by dephosphorylating proteins in the endoplasmic reticulum, leading to increased levels of calcium ions in the cytosol.Formula:C8H9ClN4Purezza:Min. 95%Peso molecolare:196.64 g/mol6-Chloro-2,2-dimethyl-2,3-dihydro-1H-inden-1-one
CAS:Versatile small molecule scaffold
Formula:C11H11ClOPurezza:Min. 95%Peso molecolare:194.66 g/mol1-(3-Methylfuran-2-yl)ethan-1-one
CAS:1-(3-Methylfuran-2-yl)ethan-1-one is a heterocyclic compound that can be found in the leaves and tubercles of Bignoniaceae plants. It is structurally related to an oxygen heterocycle, which is a class of organic compounds with oxygen in their molecular structures. 1-(3-Methylfuran-2-yl)ethan-1-one has been isolated from the leaves of Blechnum pennaefolium and the tubers of Tuberculosa leontopodioides by alkaline hydrolysis. It has shown antimicrobial activity against Gram positive bacteria. The diacetate form was isolated from the leaves of Bignonia colemanii and shown to have antiviral properties. Formylation reactions are also possible with this compound, as it has been shown to react with sodium methoxide or dimethyl sulfoxide to produce formaldehyde and methanal respectively.
Formula:C7H8O2Purezza:Min. 95%Peso molecolare:124.14 g/mol(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.Formula:C7H12O3Purezza:Min. 95%Peso molecolare: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.Formula:C9H10O2Purezza:Min. 95%Peso molecolare:150.17 g/mol4-Chloro-3,3-dimethylbutan-2-one
CAS:Versatile small molecule scaffold
Formula:C6H11ClOPurezza:Min. 95%Peso molecolare:134.6 g/mol2-(4-Aminophenyl)-2-hydroxyacetic acid
CAS:Versatile small molecule scaffoldFormula:C8H9NO3Purezza:Min. 95%Peso molecolare: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.Formula:C9H10OPurezza:Min. 95%Peso molecolare:134.17 g/mol2-(3-Methyl-4H-1,2,4-triazol-4-yl)aniline
CAS:Versatile small molecule scaffoldFormula:C9H10N4Purezza:Min. 95%Peso molecolare: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.Formula:C9H10O3Purezza:Min. 95%Peso molecolare: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.Formula:C6H7N3OPurezza:Min. 95%Peso molecolare:137.14 g/molN-(2,3-Dimethylphenyl)urea
CAS:Versatile small molecule scaffoldFormula:C9H12N2OPurezza:Min. 95%Peso molecolare:164.2 g/molN-(2-Cyanophenyl)-nprime-phenylurea
CAS:Versatile small molecule scaffoldFormula:C14H11N3OPurezza:Min. 95%Peso molecolare:237.26 g/molEthyl 2-oxo-3-(quinolin-2-yl)propanoate
CAS:Versatile small molecule scaffold
Formula:C14H13NO3Purezza:Min. 95%Peso molecolare:243.26 g/molEthyl 2,3-dicyano-3-methylpropanoate
CAS:Versatile small molecule scaffoldFormula:C8H10N2O2Purezza:Min. 95%Peso molecolare:166.18 g/mol1-(3,4-Dichlorophenyl)-3-methyl-4,5-dihydro-1H-pyrazol-5-one
CAS:Versatile small molecule scaffoldFormula:C10H8Cl2N2OPurezza:Min. 95%Peso molecolare: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.Formula:C10H14O2Purezza:Min. 95%Peso molecolare:166.22 g/mol3-Thietanecarboxylicacid,1,1-dioxide
CAS:Versatile small molecule scaffold
Formula:C4H6O4SPurezza:Min. 95%Peso molecolare:150.15 g/mol2-(Acetylamino)-4,5-dimethylthiophene-3-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C9H11NO3SPurezza:Min. 95%Peso molecolare: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 scaffoldFormula:C11H11NO2SPurezza:Min. 95%Peso molecolare: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.Formula:C9H7BrN2Purezza:Min. 95%Peso molecolare: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.
Formula:C10H9N3Purezza:Min. 95%Peso molecolare: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.
Formula:C10H8O3SPurezza:Min. 95%Peso molecolare:208.23 g/molMethyl 5-nitro-1H-pyrrole-2-carboxylate
CAS:Versatile small molecule scaffoldFormula:C6H6N2O4Purezza:Min. 95%Peso molecolare:170.12 g/mol1H-pyrrole-2-carboxylic acid, 1-methyl-5-nitro-, methyl ester
CAS:Versatile small molecule scaffoldFormula:C7H8N2O4Purezza:Min. 95%Peso molecolare:184.15 g/mol1-Methyl-4-nitro-1H-pyrrole-2-carboxamide
CAS:Versatile small molecule scaffoldFormula:C6H7N3O3Purezza:Min. 95%Peso molecolare:169.14 g/mol1-Methyl-4-nitro-1H-pyrrole-2-carboxylic acid
CAS:1-Methyl-4-nitro-1H-pyrrole-2-carboxylic acid is a molecule that has been shown to be cytotoxic to cancer cells. It interacts with the DNA at the sequences that are responsible for the production of amino acids and inhibits the synthesis of proteins. This drug also interacts with a chromophore, which is an organic molecule that absorbs light, and it can be conjugated to other molecules in order to increase its cytotoxicity. The anticancer activity of 1MNP was found to be bimodal, meaning it has different effects on different types of cancer cells.Formula:C6H6N2O4Purezza:Min. 95%Peso molecolare:170.12 g/mol2-Acetyl-1,3-thiazole-4-carboxylic acid
CAS:2-Acetyl-1,3-thiazole-4-carboxylic acid is a carbonyl compound that is structurally related to other algicides. It has been shown to be effective against marine bacteria and organisms, including algae, bacteria and fungi. The 2-acetyl derivative of 1,3-thiazole has been found to have the highest activity among the derivatives tested. The chemical structure of this compound is similar to that of methyl ester and can be easily hydrolyzed by alkaline solutions. 2-Acetyl-1,3-thiazole-4-carboxylic acid also reacts with oxygen in air to form an unstable oxide which decomposes into water and carbon dioxide. This characteristic makes it suitable for use as an algicide because it can be easily decomposed by sunlight or UV light.Formula:C6H5NO3SPurezza:Min. 95%Peso molecolare:171.18 g/mol2-Oxononanoic acid
CAS:2-Oxononanoic acid is a fatty acid that inhibits the binding of diagnostic agents to interleukin receptors. 2-Oxononanoic acid has been shown to inhibit the production of reactive oxygen species, which may be due to its acidic pH. This compound also inhibits the release of inflammatory mediators, such as cytokines and arachidonic acid metabolites. 2-Oxononanoic acid has been shown to have therapeutic potential in autoimmune diseases and infectious diseases, such as HIV/AIDS. 2-Oxononanoic acid is an affinity ligand for fatty acids and can be used in conjugates with antibodies or antigens for diagnostic purposes or therapy.
Formula:C9H16O3Purezza:Min. 95%Peso molecolare:172.22 g/mol3-(3-Hydroxyphenyl)-1-phenylurea
CAS:Versatile small molecule scaffold
Formula:C13H12N2O2Purezza:Min. 95%Peso molecolare:228.25 g/mol(2-Methoxy-5-nitrophenyl)urea
CAS:Versatile small molecule scaffoldFormula:C8H9N3O4Purezza:Min. 95%Peso molecolare:211.17 g/mol4-(Morpholin-4-yl)-N-(propan-2-yl)aniline
CAS:Versatile small molecule scaffoldFormula:C13H20N2OPurezza:Min. 95%Peso molecolare:220.31 g/mol2-Amino-6-methoxy-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile
CAS:Versatile small molecule scaffoldFormula:C10H12N2OSPurezza:Min. 95%Peso molecolare:208.28 g/mol2-Ethyl-[1,3,4]oxadiazole
CAS:Versatile small molecule scaffold
Formula:C4H6N2OPurezza:Min. 95%Peso molecolare:98.1 g/mol2-Methylcyclohex-1-ene-1-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C8H12O2Purezza:Min. 95%Peso molecolare:140.18 g/mol1-Methanesulfinyl-3-methylbenzene
CAS:1-Methanesulfinyl-3-methylbenzene is a white crystalline solid that belongs to the class of aromatic compounds. It has a melting point of 134° C and a boiling point of 350° C. 1-Methanesulfinyl-3-methylbenzene has been shown to have an x-ray crystal structure with four asymmetric units. This compound has also been analyzed by elemental analyses, which showed it contains hydrogen (H), carbon (C), sulfur (S), and oxygen (O) elements. 1-Methanesulfinyl-3-methylbenzene is soluble in organic solvents such as ethyl acetate, but insoluble in water or alcohols. It can be recrystallized from solvents such as ethyl acetate or diethyl ether. 1-Methanesulfinyl-3-methylbenzene is used for the synthesis of other organic compounds and for research purposes.Formula:C8H10OSPurezza:Min. 95%Peso molecolare:154.23 g/mol1-Methanesulfinyl-3-methoxybenzene
CAS:Versatile small molecule scaffoldFormula:C8H10O2SPurezza:Min. 95%Peso molecolare:170.23 g/mol2-Nitrocyclooctan-1-one
CAS:Versatile small molecule scaffoldFormula:C8H13NO3Purezza:Min. 95%Peso molecolare:171.2 g/mol2-Chloro-N-(2-phenylethyl)propanamide
CAS:2-Chloro-N-(2-phenylethyl)propanamide is an isoquinoline ring that has been synthesized and tested for its ability to inhibit the biosynthesis of ergosterol. It was found to be more effective than other known inhibitors, such as tetraethyl pyrophosphate, in inhibiting this compound. 2-Chloro-N-(2-phenylethyl)propanamide may be a potential drug candidate for the treatment of fungal diseases. The mechanism for inhibition is not yet known.
Formula:C11H14ClNOPurezza:Min. 95%Peso molecolare:211.69 g/mol4,4,4-Trichloro-3-hydroxybutanoic acid
CAS:4,4,4-Trichloro-3-hydroxybutanoic acid is a benzyl ester of the fatty acid 4,4,4-trichloro-3-hydroxybutanoic acid. The molecule has an optical isomer that can be synthesized from the corresponding symmetrical compound. The synthesis of 4,4,4-trichloro-3-hydroxybutanoic acid involves the reaction of benzyl alcohol with trichloromethyl chloride in the presence of an acid catalyst. This reaction yields two isomers: one of which has the same configuration as the starting material and one that is an optical isomer. The latter can be converted to its antipode by hydrogenation or by heating with sodium methoxide in methanol.Formula:C4H5Cl3O3Purezza:Min. 95%Peso molecolare:207.43 g/mol2-{[(3-Chlorophenyl)amino]methyl}phenol
CAS:Versatile small molecule scaffoldFormula:C13H12ClNOPurezza:Min. 95%Peso molecolare:233.69 g/mol4-Amino-N-pyridin-3-ylbenzamide
CAS:Versatile small molecule scaffold
Formula:C12H11N3OPurezza:Min. 95%Peso molecolare:213.24 g/mol2-Bromohexanamide
CAS:2-Bromohexanamide is a receptor binding molecule that binds to the 5-HT2A receptor. 2-Bromohexanamide has been shown to be effective in treating autoimmune diseases, including psoriasis and rheumatoid arthritis. It is also used for the treatment of cancer, specifically for the prevention of chemotherapy-induced nausea and vomiting. 2-Bromohexanamide has been shown to bind to the 5-HT7 receptor, which is involved in regulating mood and appetite. The drug has a hydroxyl group that reacts with nucleophilic attack at the amide bond to form an acid complex. This reaction mechanism results in a molecule that can bind to receptors and cause receptor activity.Formula:C6H12BrNOPurezza:Min. 95%Peso molecolare:194.07 g/mol7-Chloro-2,3-dihydro-3-phenyl-2-thioxo-1H-quinazolin-4-one
CAS:Versatile small molecule scaffoldFormula:C14H9ClN2OSPurezza:Min. 95%Peso molecolare:288.75 g/mol2-Methoxybenzene-1-sulfinic acid
CAS:2-Methoxybenzene-1-sulfinic acid is a synthetic drug that has been used as an anti-schistosomiasis agent. It is structurally related to the natural substrate of the enzyme schistosomal beta-ketoacyl synthase, and has been shown to inhibit this enzyme in vivo with a potency similar to that of praziquantel.
Formula:C7H8O3SPurezza:Min. 95%Peso molecolare:172.2 g/mol1,2,3,4,5-Pentamethyl-6-nitrobenzene
CAS:The chemical name for 1,2,3,4,5-Pentamethyl-6-nitrobenzene is 6-Nitroso-1,1′-(3,3′-dimethylpropyl)-1,2,3,-4,5-pentamethylbenzene. It is a colorless liquid that has a boiling point of 190 °C and density of 1.0 g/mL. 6NMN is soluble in acetone and ethanol but insoluble in water. This compound has been shown to be an effective antihypertensive agent with reversible vasodilator properties. Clinical development of 6NMN has been hindered by the lack of a suitable animal model for congestive heart failure (CHF). There are no known functional groups on this molecule; however it does have a phenolic group at the para position and hydroxyl group at the meta position on the benzene ring. The compound also has two nitro groups thatFormula:C11H15NO2Purezza:Min. 95%Peso molecolare:193.24 g/molBenzenemethanamine, N-cyclohexyl-3,4-dimethoxy-, hydrochloride
CAS:Versatile small molecule scaffoldFormula:C15H24ClNO2Purezza:Min. 95%Peso molecolare:285.81 g/molTetrafluoropyrazine
CAS:Tetrafluoropyrazine is a fluorinated electrophilic compound that serves as an oxygen nucleophile. It reacts with hydrochloric acid and chlorine to form hydrogen chloride and tetrafluoropyrazine hydrochloride, respectively. Tetrafluoropyrazine has been shown to bind to the 5-HT7 receptor in rat brains, which may be due to its chemical similarity to serotonin. Magnetic resonance spectroscopy revealed that tetrafluoropyrazine contains nitrogen atoms in its structure. The polymer film structure of this molecule was determined by X-ray crystallography. Tetrafluoropyrazine also has the ability to oxidize polyethylene glycols and polypropylene glycols, which may be due to its ability to act as an electron acceptor.Formula:C4F4N2Purezza:Min. 95%Peso molecolare:152.05 g/mol1-(Oxan-2-yl)propan-2-one
CAS:Versatile small molecule scaffoldFormula:C8H14O2Purezza:Min. 95%Peso molecolare:142.2 g/mol4-Oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C16H11NO3Purezza:Min. 95%Peso molecolare:265.26 g/mol4-Hydroxy-2-(iso-propyl)quinazoline
CAS:Versatile small molecule scaffoldFormula:C11H12N2OPurezza:Min. 95%Peso molecolare:188.23 g/molN-Phenyl-1H-imidazole-5-carboxamide
CAS:Versatile small molecule scaffold
Formula:C10H9N3OPurezza:Min. 95%Peso molecolare:187.2 g/mol2,3-Ddihydro-2,2-dimethyl-4H-1-benzothiopyran-4-one 1-oxide
CAS:Versatile small molecule scaffoldFormula:C11H12O2SPurezza:Min. 95%Peso molecolare:208.28 g/mol5-Cyclohexylthiophene-3-carboxylic acid
CAS:Versatile small molecule scaffoldFormula:C11H14O2SPurezza:Min. 95%Peso molecolare:210.29 g/mol2-Hydroxy-2,3-dihydro-1H-indene-2-carboxylic acid
CAS:Versatile small molecule scaffold
Formula:C10H10O3Purezza:Min. 95%Peso molecolare:178.18 g/mol2-chloro-5-nitrothiophene
CAS:2-Chloro-5-nitrothiophene is a nucleophilic compound that reacts with acetonitrile, which is a nucleophile. The inhibitory concentration of 2-chloro-5-nitrothiophene has been shown to be lower than that of thiophenes in general, and the compound can be used as a tool for evaluating the biological activity of thiophenes. 2-Chloro-5-nitrothiophene has been shown to have good inhibitory effects on Escherichia coli and other organisms. This compound also induces a number of different reactions: heterocyclic ring formation, synthesis of acetonitrile, and biomolecule evaluation.
Formula:C4H2ClNO2SPurezza:Min. 95%Peso molecolare:163.58 g/mol4-(Ethylthio)benzoic acid
CAS:4-(Ethylthio)benzoic acid is a stabilizer and biotransformation product of salicylic acid. It is synthesized by the demethylation of 4-hydroxybenzoic acid, which is an intermediate in the synthesis of salicylic acid. 4-(Ethylthio)benzoic acid has been shown to be a potent inhibitor of bacterial cytochrome P450 enzymes and may be useful as an antibacterial agent against bacteria that are resistant to other antibiotics. The nature and mechanism of its action on bacterial cytochrome P450 enzymes is not well understood at this time.Formula:C9H10O2SPurezza:Min. 95%Peso molecolare:182.24 g/mol4-(Isopropylsulfanyl)benzoic acid
CAS:4-(Isopropylsulfanyl)benzoic acid is a disubstituted benzoic acid with a 4-isopropylsulfanyl substituent. The compound is an analog of 4-methoxybenzoic acid and has been shown to be complementary to the same target site. Analogously, it also has been shown to have similar regiochemistry and ortho substitution as 4-methoxybenzoic acid.Formula:C10H12O2SPurezza:Min. 95%Peso molecolare:196.27 g/mol2-Bromo-2-methylpropanal
CAS:2-Bromo-2-methylpropionaldehyde is an organic compound that belongs to the class of propionates. It is a primary amine that can be synthesized from acetone and chloroform. 2-Bromo-2-methylpropionaldehyde has been used as a disinfectant for skin and mucous membranes. It also lowers blood pressure by dilating the veins, which can help to prevent strokes and heart attacks. 2-Bromo-2-methylpropionaldehyde is more labile than its parent compound, propionic acid, because it lacks the hydrogens on the methyl group. It is susceptible to oxidation by hypobromous acid or chloride ions, which can lead to the formation of phenacyl bromide. Phenacyl bromide has been shown to have antiseptic properties and can be used as an intermediate in organic synthesis. END>>Formula:C4H7OBrPurezza:Min. 95%Peso molecolare:151 g/mol3-(Hydroxyimino)-7-methyl-2,3-dihydro-1H-indol-2-one
CAS:Versatile small molecule scaffold
Formula:C9H8N2O2Purezza:Min. 95%Peso molecolare:176.17 g/mol3,3-Dimethylbicyclo[2.2.1]heptan-2-one
CAS:3,3-Dimethylbicyclo[2.2.1]heptan-2-one is a reactive compound that belongs to the group of psychostimulants. It has been shown to be effective against cancer cells and is used in the treatment of cancer patients. There are two possible reaction mechanisms: 1) the formation of an intermediate (a cation), which then reacts with water vapor, and 2) a direct reaction between 3,3-dimethylbicyclo[2.2.1]heptan-2-one and water vapor. The former mechanism is more probable because it requires less energy input than the latter one. The quantum theory states that 3,3-dimethylbicyclo[2.2.1]heptan-2-one has an activation energy of ˜120 kJ/mol (or ˜135 kJ/mol).Formula:C9H14OPurezza:Min. 95%Peso molecolare:138.21 g/mol1,4-Dihydrobenzo[d][1,3]oxazin-2-one
CAS:1,4-Dihydrobenzo[d][1,3]oxazin-2-one is an organic solvent that can be used in the synthesis of quinoline derivatives. It is a carbamate that has been used as an efficient method for preparing chloroformates. In addition, 1,4-Dihydrobenzo[d][1,3]oxazin-2-one has been shown to be a potent progesterone receptor modulator.Formula:C8H7NO2Purezza:Min. 95%Peso molecolare:149.15 g/mol4-Phenylbutylamine
CAS:4-Phenylbutylamine is a chemical that is found in natural compounds. It is a monoclonal antibody that binds to insulin-stimulated glucose, which is a type of protein. This binding inhibits the activity of 4-hydroxycinnamic acid and other enzymes, thereby reducing the amount of kinetic energy generated by these reactions. The binding also reduces the number of amines present in the sample. 4-Phenylbutylamine can be used for kinetic studies because it has low molecular weight and high stability.Formula:C10H15NPurezza:Min. 95%Peso molecolare:149.24 g/molrac-(2R,3R)-3-Phenyloxolane-2-carboxylic acid
CAS:Versatile small molecule scaffold
Formula:C11H12O3Purezza:Min. 95%Peso molecolare:192.21 g/mol6-Methoxy-3-methyl-2,3,4,9-tetrahydro-1H-carbazole
CAS:Versatile small molecule scaffoldFormula:C14H17NOPurezza:Min. 95%Peso molecolare:215.29 g/mol2-Bromo-5,7-dimethyl[1,2,4]triazolo[1,5-a]pyrimidine
CAS:Please enquire for more information about 2-Bromo-5,7-dimethyl[1,2,4]triazolo[1,5-a]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C7H7BrN4Purezza:Min. 95%Peso molecolare:227.06 g/mol[1,2,4]Triazolo[1,5-a]pyrimidin-2-ylamine
CAS:[1,2,4]Triazolo[1,5-a]pyrimidin-2-ylamine is a heterocyclic compound that is used to treat hematological and inflammatory diseases. It has been shown to have a long-term effect in treating autoimmune diseases and neurodegenerative diseases. It is also an aromatic hydrocarbon that can be used as a drug for the treatment of gastroenterological conditions such as ulcers or Crohn's disease.Formula:C5H5N5Purezza:Min. 95%Peso molecolare:135.13 g/mol2-(Prop-2-yn-1-yl)oxane
CAS:Versatile small molecule scaffoldFormula:C8H12OPurezza:Min. 95%Peso molecolare:124.2 g/molmethyl 2-amino-2-(4-methoxyphenyl)acetate hydrochloride
CAS:Versatile small molecule scaffoldFormula:C10H14ClNO3Purezza:Min. 95%Peso molecolare:231.7 g/molMethyl 2-amino-2-(naphthalen-1-yl)acetate hydrochloride
CAS:Versatile small molecule scaffoldFormula:C13H14ClNO2Purezza:Min. 95%Peso molecolare:251.71 g/mol3-Bromo-1-(3,4-dichlorophenyl)pyrrolidin-2-one
CAS:Versatile small molecule scaffoldFormula:C10H8BrCl2NOPurezza:Min. 95%Peso molecolare:308.98 g/mol2-Hydrazinyl-5-phenyl-1,3,4-thiadiazole
CAS:Versatile small molecule scaffoldFormula:C8H8N4SPurezza:Min. 95%Peso molecolare:192.24 g/molN-Methyl-N-phenylmethanesulfonamide
CAS:N-Methyl-N-phenylmethanesulfonamide (NMPSA) is a small molecule that has been used as an anticancer agent in human cell cultures. NMPSA inhibits the growth of cancer cells by inducing apoptosis and arrest of the cell cycle, which may be due to its ability to inhibit tyrosine kinase activity. It also inhibits the production of reactive oxygen species (ROS), which are thought to play a role in tumorigenesis. NMPSA has been shown to be more potent than other anticancer drugs on a per weight basis, with an EC50 value of 0.1 μM.Formula:C8H11NO2SPurezza:Min. 95%Peso molecolare:185.25 g/mol6-Methoxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one
CAS:Versatile small molecule scaffoldFormula:C12H14O3Purezza:Min. 95%Peso molecolare:206.24 g/mol4-Nitro-1-propyl-1H-imidazole
CAS:Versatile small molecule scaffold
Formula:C6H9N3O2Purezza:Min. 95%Peso molecolare:155.15 g/mol2,5-Dimethoxybenzene-1,4-diol
CAS:2,5-Dimethoxybenzene-1,4-diol is an intermediate in the synthesis of salicylic acid. It is a reagent that is used to produce hydrogen peroxide and can be used for the determination of salicylic acid. 2,5-Dimethoxybenzene-1,4-diol can be used as a reducing agent and chelator. It also exhibits anti-fungal properties and has been shown to have anti-inflammatory effects. The mechanism by which 2,5-dimethoxybenzene-1,4-diol reduces radicals is not well understood but may involve the conversion of hydrogen peroxide into water and oxygen gas.Formula:C8H10O4Purezza:Min. 95%Peso molecolare:170.16 g/mol4-Aminoanisole-3-sulfonic acid
CAS:4-Aminoanisole-3-sulfonic acid is a nitro compound that is used as a buffer and pH stabilizer. It is synthesized by the reaction of methoxyaniline with sulfonic acids. 4-Aminoanisole-3-sulfonic acid has been shown to react with x-rays, forming an optical sensor. This chemical can also be used to synthesize other sulfonated compounds such as sulfonates and sulfites. This compound can be prepared by the addition of hydrochloric acid to zinc powder followed by the addition of hydrogen sulfate, which gives the final product in a chlorinated form.Formula:C7H9NO4SPurezza:Min. 95%Peso molecolare:203.22 g/mol2,4-Bis(benzyloxy)benzaldehyde
CAS:2,4-Bis(benzyloxy)benzaldehyde is a prenylated aromatic compound that has been shown to have potent tyrosinase inhibitory activity. This effect was seen in murine melanoma cells and was found to be reversible. 2,4-Bis(benzyloxy)benzaldehyde also showed an inhibitory effect on the production of phytoalexins in plants. When combined with hydrochloric acid, 2,4-Bis(benzyloxy)benzaldehyde inhibits tyrosinase activity by interacting with the chloride ion on the enzyme's active site.
Formula:C21H18O3Purezza:Min. 95%Peso molecolare:318.37 g/molEthyl 2,4-dioxohexanoate
CAS:Ethyl 2,4-dioxohexanoate (EDOH) is a bioactive molecule that can be used as a disinfectant. It reacts with propionyl to form an acid carboxylate, which has been shown to have antimicrobial activity against bacteria and fungi. EDOH is also used in the synthesis of heterocyclic compounds such as tebufenpyrad. The reaction yield and time depend on the solvent used. For instance, EDOH reacts better in dimethylformamide than in water or methanol. Reaction of EDOH with phenoxy leads to amide formation and subsequent cyclization to form a new ring system.Formula:C8H12O4Purezza:Min. 95%Peso molecolare:172.18 g/mol1-(2-Bromoethoxy)naphthalene
CAS:Versatile small molecule scaffold
Formula:C12H11BrOPurezza:Min. 95%Peso molecolare:251.12 g/mol2-(2-bromoethoxy)naphthalene
CAS:2-(2-bromoethoxy)naphthalene (2BEEN) is a white or light yellow crystalline solid. It has a molecular weight of 198.8 and an empirical formula of C14H16BrO. 2BEEN is structurally related to piperazine, but the bromine atom at the 2 position in 2BEEN provides a linkage with the ethoxy group at the 4 position, which can orient in two possible orientations. The compound exhibits cis-trans conformational torsion and dihedral angles that are similar to those found in piperazine.Formula:C12H11OBrPurezza:Min. 95%Peso molecolare:251.11 g/mol3-(1,3-Dioxolan-2-yl)thiophene-2-carbaldehyde
CAS:Versatile small molecule scaffoldFormula:C8H8O3SPurezza:Min. 95%Peso molecolare:184.21 g/mol2,3-Thiophenedimethanol
CAS:Versatile small molecule scaffoldFormula:C6H8O2SPurezza:Min. 95%Peso molecolare:144.19 g/molEthyl 4-hydroxy-7-methyl-1,8-naphthyridine-3-carboxylate
CAS:Versatile small molecule scaffold
Formula:C12H12N2O3Purezza:Min. 95%Peso molecolare:232.23 g/mol4-Hydroxy-7-methyl-[1,8]naphthyridine-3-carboxylic acid
CAS:4-Hydroxy-7-methyl-[1,8]naphthyridine-3-carboxylic acid is a compound that has been shown to be an antibacterial agent. It has been shown to selectively inhibit the growth of Gram-positive bacteria by binding to the bacterial cell wall. 4-Hydroxy-7-methyl-[1,8]naphthyridine-3-carboxylic acid binds to amino acids in the peptidoglycan layer of the bacterial cell wall and inhibits the crosslinking of these amino acids with divalent ions such as calcium and magnesium. This leads to changes in solvation structures and decreases in hydrogen bonding interactions, which reduces the stability of the peptidoglycan layer. The spectrum for this molecule is anharmonic, which means that it does not have a harmonic frequency but instead has many frequencies that are related by integer numbers. The molecule can exist in three different forms: two tautomers (keto formFormula:C10H8N2O3Purezza:Min. 95%Peso molecolare:204.18 g/mol[1,2,4]Triazolo[4,3-a]pyrazin-3-amine
CAS:Versatile small molecule scaffold
Formula:C5H5N5Purezza:Min. 95%Peso molecolare:135.13 g/mol8-Aminonaphthalene-2-sulfonamide
CAS:Versatile small molecule scaffold
Formula:C10H10N2O2SPurezza:Min. 95%Peso molecolare:222.3 g/mol(Pyridin-4-yl)urea
CAS:(Pyridin-4-yl)urea is a ligand with affinity for the neurohormonal receptor urotensin. The binding affinity of this ligand to the urotensin receptor is in the low nanomolar range. (Pyridin-4-yl)urea binds to the urotensin receptor with a higher affinity than its natural ligands, which are small peptides. This compound has been shown to act as a potent antagonist of urotensin, inhibiting its function and blocking the release of its natural agonists, vasopressin and oxytocin. (Pyridin-4-yl)urea has also been shown to inhibit the binding of vasopressin or oxytocin to their specific receptors on cells, which may lead to an increased production of these hormones in vitro.Formula:C6H7N3OPurezza:Min. 95%Peso molecolare:137.14 g/mol(2-Phenylphenyl)urea
CAS:Versatile small molecule scaffoldFormula:C13H12N2OPurezza:Min. 95%Peso molecolare:212.25 g/mol(4-Phenylphenyl)urea
CAS:The molecular formula of 4-Phenylphenyl)urea is C8H7N3O2 and its molecular weight is 186.19 g/mol. The chemical name for 4-Phenylphenyl)urea is (4-phenylphenyl) urea. It has a melting point of 192°C, a boiling point of 334°C, and a density of 1.12 g/cm3. 4-Phenylphenyl)urea crystallizes in the orthorhombic system with space group Pbca and lattice constants a = 8.068 Å, b = 7.957 Å, c = 12.096 Å and β = 116°. It has hydrogen bonds to water molecules as well as to itself through hydrogen bonds with the amide NH groups on the urea moiety and the phenyl ring on one molecule forming hydrogen bonds with other phenyl rings on adjacent molecules.Formula:C13H12N2OPurezza:Min. 95%Peso molecolare:212.25 g/molN-(Chloroacetyl)allylamine
CAS:Versatile small molecule scaffold
Formula:C5H8ClNOPurezza:Min. 95%Peso molecolare:133.58 g/mol2-(2-Bromophenyl)-1H-benzimidazole
CAS:2-(2-Bromophenyl)-1H-benzimidazole is a halogenated aromatic compound that has been used in electrochemical studies. It can be synthesized by the reaction of bromine with 2,4-dinitrobenzene. The compound exhibits a number of functional groups including nitro and bromo groups. One of the most notable properties of this compound is its ability to act as an efficient electrocatalyst for the reduction of chloride ions to hydrogen gas. 2-(2-Bromophenyl)-1H-benzimidazole also has potentiodynamic polarization properties and has been shown to catalyze the reduction of a number of organic compounds including propane, butane, pentane, hexane and heptane. This compound is also used in microscopy simulations to study unsymmetrical molecules.Formula:C13H9BrN2Purezza:Min. 95%Peso molecolare:273.13 g/mol3-Hydroxy-3-phenylpentanoic acid
CAS:3-Hydroxy-3-phenylpentanoic acid is a chiral compound with two stereoisomers, the L and D configurations. The L form has been shown to be an enantiomer of propiophenone, which is an ester that reacts in the presence of acetate and hydrogen chloride to form 3-hydroxy-3-phenylpentanoic acid acetate. This reaction is a condensation reaction. The D form has been shown to be an enantiomer of propiophenone, which is an ester that reacts in the presence of acetate and hydrogen chloride to form 3-hydroxy-3-phenylpentanoic acid acetate. This reaction is a condensation reaction. 3HPP can also be synthesized by asymmetric synthesis or hydrolysis.Formula:C11H14O3Purezza:Min. 95%Peso molecolare:194.23 g/mol2-[(2-Methoxyphenyl)amino]benzoic acid
CAS:Versatile small molecule scaffoldFormula:C14H13NO3Purezza:Min. 95%Peso molecolare:243.26 g/mol4-(4-Methylphenyl)-3-thiosemicarbazide
CAS:4-(4-Methylphenyl)-3-thiosemicarbazide is a carbonyl compound. It has been shown to be an inhibitor of acetylcholinesterase, an enzyme that breaks down the neurotransmitter acetylcholine, which is involved in muscle contraction. This inhibition causes paralysis and death in insects. 4-(4-Methylphenyl)-3-thiosemicarbazide has also been shown to be active against gram-negative bacteria. The structure of this molecule was determined by its vibrational spectra and multinuclear NMR data. 4-(4-Methylphenyl)-3-thiosemicarbazide stabilizes the dihedral angle between two nitrogen atoms, which are necessary for formation rate.
Formula:C8H11N3SPurezza:Min. 95%Peso molecolare:181.26 g/mol4-Bromobut-2-yn-1-ol
CAS:4-Bromobut-2-yn-1-ol is a chemical compound belonging to the group of thyroid hormones. It is a potent thyromimetic that has been used in cancer research and genetic disease studies. 4-Bromobut-2-yn-1-ol binds to hormone receptors, thereby initiating a response in cells. This compound has been shown to induce mutations in colorectal adenocarcinoma cells, as well as gene expression changes in mutant cells. 4-Bromobut-2-yn-1-ol is also cardiotoxic, with an ID50 value of 0.06 mg/kg body weight.Formula:C4H5BrOPurezza:Min. 95%Peso molecolare:148.99 g/molMethyl 2,2-dibromo-2-cyanoacetate
CAS:Versatile small molecule scaffoldFormula:C4H3Br2NO2Purezza:Min. 95%Peso molecolare:256.88 g/mol
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