Building Blocks

5-Amino-2-phenyl-2H-1,2,3-triazole-4-carboxamide

<p>1-(Trifluoroacetyl)piperidin-4-one</p>

<p>2,6-Dichloro-N-(N,N-dimethylcarbamimidoyl)isonicotinamide</p>

<p>Piperidin-4-one hydrochloride hydrate</p>

<p>4-(3-Pentyl)pyridine</p>

<p>1-(2,6-Difluorobenzoyl)piperidin-4-one</p>

2,3,5,6-Tetrafluoropyridine

<p>5-(4-Nitrophenyl)-2H-tetrazole-2-acetic acid</p>

<p>5-(2,3-Dichlorophenyl)-1H-tetrazole</p>

<p>2-Bromo-4,5,6,7-tetrahydrothiazolo[4,5-c]pyridine</p>

<p>Piperidin-4-one, N-BOC protected</p>

<p>Thiophene</p>

4,4'-Bipyridine dihydrochloride

<p>1-Benzoylpiperidin-4-one</p>

4-Bromo-5-methylisatin

<p>Imipenem monohydrate</p>

<p>N-Acetylpiperidin-4-one</p>

<p>Piperidin-4-one, N-CBZ protected</p>

(Piperidin-1-yl)acetic acid hydrochloride

<p>5-Hydroxyindole-2-carboxylic acid ethyl ester is a fluorescent probe that is used in the detection of hepatitis C virus by micropet assay. The compound reacts with amines and undergoes fluorescence quenching, and can be used to quantitate their concentration. 5-Hydroxyindole-2-carboxylic acid ethyl ester is also used for the determination of the kinetics of amines and other compounds that are involved in the metabolism of drugs and biogenic amines. It can be applied to chromatographic analysis or sample preparation prior to analysis by analytical chemistry methods such as gas chromatography or liquid chromatography.</p>

<p>1,2,3,6-Tetrahydropyridine is an experimental drug that acts as a dopamine receptor antagonist. It has been shown to induce neuronal death in the presence of excess dopamine by inhibiting the uptake of dopamine by neurons. The nitrogen atom in position 6 may be involved in binding to the receptor and initiating the conformational change needed for activation. Tetrahydropyridine binds to the D1 and D2 receptors with high affinity, but it does not bind to D4 receptors. Tetrahydropyridine can also inhibit locomotor activity in mice and rats.</p>

<p>Diphenylmethane is a chemical that has been used in the synthesis of pharmaceuticals and other organic compounds. It is also a useful reagent for the preparation of synthetic amines. Diphenylmethane can be used to synthesize drugs such as epidermal growth factor, which stimulates the growth and differentiation of keratinocytes. This chemical also has a number of potential therapeutic uses for metabolic disorders and infectious diseases, including hepatitis. The mechanism by which this compound reacts with nitrogen atoms is not fully understood, but it may involve the formation of diphenylmethanesulfinic acid.</p>

<p>7-Azaindole is a reactive chemical that has been shown to be effective in the treatment of skin cancer, as well as hepatic steatosis. The compound can promote the transfer of hydrogen atoms and form a dimer with protonated nitrogen. 7-Azaindole reacts rapidly with nucleophiles such as amines, alcohols, and thiols to form covalent bonds. The reaction mechanism is characterized by an initial protonation step followed by nucleophilic attack or hydrogen transfer from the nucleophile to 7-azaindole. Kinetic studies have demonstrated that the rate of this reaction depends on the concentration of both reactants.</p>

<p>6-Azaindole is a fine chemical that can be used as a reagent, building block, and intermediate. It is a versatile compound that has been shown to have high quality and complex chemistry. 6-Azaindole is an important reaction component in the synthesis of other compounds with pharmaceutical applications such as amide synthons, amino acid esters, and pharmaceutical intermediates. 6-Azaindole can also be used as a scaffold for the preparation of indoles. CAS No: 271-29-4</p>

<p>N-Acetyl-L-alanine is the N-acetylated form of L-alanine and is a nonessential amino acid. It is an amide containing one nitrogen atom and two carbonyl groups. The nitrogen can be found in either the alpha or beta position on the amide. The biological properties of N-acetyl-L-alanine are similar to those of L-alanine, as it is used as a substrate for protein synthesis and has been shown to inhibit p21 and epidermal growth factor. The conformational properties of N-acetyl-L-alanine are different from that of L-alanine due to its changed shape, which may affect its biological activity.</p>

<p>2'-Methoxyacetophenone is a member of the class of halogenated phenols that exhibits anti-inflammatory activities. It inhibits protease activity in vitro and has been shown to have anti-inflammatory effects in vivo. 2'-Methoxyacetophenone is a ruthenium complex with hydrochloride salt that has been shown to be an efficient catalyst for acylation reactions. This compound also inhibits the transfer of the nerve impulse from the trigeminal nerve to the brain, which may be due to its ability to inhibit lipid peroxidation and protein autoxidation. 2'-Methoxyacetophenone has also been shown to have antimicrobial activity against gram-negative bacterial species, such as Proteus vulgaris, Escherichia coli, Pseudomonas aeruginosa, and Salmonella enterica.</p>

<p>Please enquire for more information about 3,3',5,5'-Tetramethylbenzidine, free base including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>