Aminas
Subcategorias de "Aminas"
- Nitrosaminas(2.606 produtos)
- Aminas primárias(30.948 produtos)
- Catiões Quaternários de Amónio(1.100 produtos)
- Aminas secundárias(20.886 produtos)
- Aminas terciárias(17.195 produtos)
Foram encontrados 8786 produtos de "Aminas"
3-Hydroxy-4-amino-butyric acid
CAS:Produto Controlado3-Hydroxy-4-amino-butyric acid is a synthetase that catalyzes the formation of 3-hydroxy-4 amino butyric acid from 3-hydroxy butyric acid and ammonia. This reaction occurs in the presence of chloride ions, ethyl bromoacetate and butyric acid. The isolated yield of this reaction is 47%. The product can be converted to 3-amino butyric acid by dehydrating it with hydrochloric acid. 3-Hydroxy-4 amino butyric acid has been shown to have anticancer properties in vitro. It also has been shown to have antiinflammatory properties, which may be due to its ability to inhibit the production of prostaglandin E2, an inflammatory mediator.Fórmula:C4H9NO3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:119.12 g/mol[2-(5-Chloro-1H-indol-3-yl)-1-methylethyl]amine hydrochloride
CAS:Produto ControladoPlease enquire for more information about [2-(5-Chloro-1H-indol-3-yl)-1-methylethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C11H13ClN2Pureza:Min. 95%Peso molecular:208.69 g/mol3-Methylphenethylamine
CAS:Produto Controlado3-Methylphenethylamine is a synthetic amine that is used in the production of 3-methylphenethylamine hydrochloride. It has been shown to have a wide range of pharmacological effects, including increasing blood pressure, heart rate, and respiration. This drug also has an antitussive effect and can be used to treat asthma symptoms. 3-Methylphenethylamine can be synthesized by reacting phenylethylamine with formaldehyde and hydrogen chloride gas in the presence of alcohol or sodium hydroxide solution.Fórmula:C9H13NPureza:Min. 95%Peso molecular:135.21 g/mol3-Chloro-N-methylpropan-1-amine HCl
CAS:Please enquire for more information about 3-Chloro-N-methylpropan-1-amine HCl including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C4H11Cl2NPureza:Min. 95%Peso molecular:144.04 g/mol5-[3-(Dimethylamino)propyl]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol
CAS:Please enquire for more information about 5-[3-(Dimethylamino)propyl]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C20H25NOPureza:Min. 95%Cor e Forma:Beige SolidPeso molecular:295.42 g/molN-[3-Fluoro-4-[(methylamino)carbonyl]phenyl]-2-methylalanine
CAS:Please enquire for more information about N-[3-Fluoro-4-[(methylamino)carbonyl]phenyl]-2-methylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C12H15FN2O3Pureza:Min. 95%Peso molecular:254.26 g/mol(S)-2-Azido isovaleric acid cyclohexylammonium
CAS:Please enquire for more information about (S)-2-Azido isovaleric acid cyclohexylammonium including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C6H13N•C5H9N3O2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:242.32 g/mol4-Amino-3,5-difluorobenzonitrile
CAS:4-Amino-3,5-difluorobenzonitrile is a fine chemical used as a building block in research chemicals, reagent, and speciality chemical. It is versatile and can be used as a reaction component in the synthesis of complex compounds with various applications. CAS No. 110301-23-0 is an important intermediate for the synthesis of organic compounds and pharmaceuticals. 4-Amino-3,5-difluorobenzonitrile is also used as a scaffold for the synthesis of organic compounds.Fórmula:C7H4F2N2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:154.12 g/mol2-[(Dimethylamino)methylene]-5-(2,3,4-trimethoxyphenyl)cyclohexane-1,3-dione
CAS:Produto ControladoPlease enquire for more information about 2-[(Dimethylamino)methylene]-5-(2,3,4-trimethoxyphenyl)cyclohexane-1,3-dione including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C18H23NO5Pureza:Min. 95%Peso molecular:333.38 g/molcis-Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II)
CAS:Produto ControladoPlease enquire for more information about cis-Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II) including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C6H16Cl2N2PdPureza:Min. 95%Peso molecular:293.53 g/mol2-(tert-Butylamino)-4,6-dichloro-1,3,5-triazine
CAS:Please enquire for more information about 2-(tert-Butylamino)-4,6-dichloro-1,3,5-triazine including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C7H10Cl2N4Pureza:Min. 95%Peso molecular:221.09 g/mol2-Amino-7-Benzyl-1H-Purin-6(7H)-One
CAS:Please enquire for more information about 2-Amino-7-Benzyl-1H-Purin-6(7H)-One including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C12H11N5OPureza:Min. 95%Peso molecular:241.25 g/mol2-(2-Bromophenyl)ethanamine
CAS:Produto Controlado2-(2-Bromophenyl)ethanamine is a new and efficient method for the amination of imines with methyl groups. This process involves the use of catalytic amounts of N-bromosuccinimide (NBS) in the presence of 2,6-lutidine to form a cyclic imine intermediate. The reaction is carried out at room temperature and the yield can be as high as 99%. The reaction shown here is an example of an asymmetric amination reaction.Fórmula:C8H10BrNPureza:Min. 95%Cor e Forma:Colorless Clear LiquidPeso molecular:200.08 g/mol2-Chloro-3,4-dimethoxyphenethylamine HCl
CAS:Produto Controlado2-Chloro-3,4-dimethoxyphenethylamine is an intermediate in the synthesis of zepines. It can be synthesized by reduction of borohydride with 2-chloro-1,2,3,4-tetrahydrobenzaldehyde.Pureza:Min. 95%4-Aminoisoxazole
CAS:4-Aminoisoxazole is a triazole that has been found to be active against tumor cell lines. It is synthesized by reacting zinc powder with an acid solution containing 4-nitrobenzaldehyde, which results in the formation of 4-aminobenzonitrile, which subsequently undergoes nitration and reduction to form 4-aminoisoxazole. The synthesis of this compound can also be achieved by reacting ammonium nitrate with nitric acid in the presence of hydrochloric acid.Fórmula:C3H4N2OPureza:Min. 95%Peso molecular:84.08 g/molN-[1,1'-Biphenyl]-4-yl-9,9-dimethyl-9H-fluoren-2-amine
CAS:N-Biphenyl-4-yl-9,9-dimethyl-9H-fluoren-2-amine is a fluorescent probe that is used in fluorescence spectroscopy, chemiluminescence detection, and electron spin resonance. It has been shown to be selective for metal ions such as Cu(II), Fe(III), and Mn(II) in the presence of thioacetal. The probe can be synthesized by reacting 4-(phenylazo)benzoic acid with 9,9'-dimethoxybiphenyl. In addition to being a probe, N-Biphenyl-4-yl-9,9'-dimethyl-9H -fluoren 2 amine has been used as an herbal medicine to treat cancer and other diseases in China.
Fórmula:C27H23NPureza:Min. 95%Peso molecular:361.48 g/mol(1R,2R)-1-Amino-2-benzyloxycyclopentane
CAS:(1R,2R)-1-Amino-2-benzyloxycyclopentane is achiral. It is a synthetic chemical that has been used as an initiator for polymerization of amines and hexafluoroisopropanol. The synthesis of this compound can be achieved through a chiral technique known as interfacial polymerization. (1R,2R)-1-Amino-2-benzyloxycyclopentane is an initiator for the production of polymers with alternating helical chains. This process relies on the presence of achiral molecules to initiate the polymerization process.
Fórmula:C12H17NOPureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:191.27 g/mol2-(2-Aminoethoxy)ethanol
CAS:2-(2-Aminoethoxy)ethanol (2-AE) is a natural compound that has been synthesized from ethanol and 2-aminoethanol. It has been shown to react with sodium carbonate to form stable complexes that are resistant to hydrolysis by amines. The stability of the complex is attributed to the formation of an intermolecular hydrogen bond between the hydroxyl group on the 2-AE molecule and the carboxylate group on the sodium carbonate molecule. 2-AE reacts with benzalkonium chloride, a quaternary ammonium salt, in water vapor to produce an alcohol and a fatty acid, which is then hydrolyzed by glycol ethers into glycolates. This mechanism is similar to that of other reactions involving quaternary ammonium salts, such as those in fatty acids or glycol ethers.
Fórmula:C4H11NO2Pureza:Min. 95%Peso molecular:105.14 g/mol4-Benzyloxy-3-methoxy-N-methylphenethylamine hydrochloride
CAS:Produto ControladoPlease enquire for more information about 4-Benzyloxy-3-methoxy-N-methylphenethylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C17H22ClNO2Pureza:Min. 95%Peso molecular:307.81 g/mol(R)-1-Boc-3-(aminomethyl)pyrrolidine
CAS:Please enquire for more information about (R)-1-Boc-3-(aminomethyl)pyrrolidine including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C10H20N2O2Pureza:Min. 95%Peso molecular:200.28 g/mol
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