Benzamides

4-Hydroxybenzamide is a fatty acid with the hydroxyl group at the 4 position. It has been shown to inhibit the activity of human protein by interfering with hydrogen bonding and amide formation. The chemical structures of 4-hydroxybenzamide have been studied by electrochemical impedance spectroscopy (EIS) and found to be a competitive inhibitor of 1-hydroxy-2-naphthoic acid, an adenosine receptor antagonist, and p-hydroxybenzoic acid. This compound has also been shown to be acutely toxic in rats at high doses.

TMB is an excellent colorimetric substrate for detection of horseradish peroxidase labelled probes and is used with peroxidase and peroxidase coupled systems, particularly in ELISA techniques. It produces a soluble end product, which is blue in color and can be read spectrophotometrically. TMB has also been used in the quantitative determination of hemoglobin and in cytochemical staining for peroxidase. TMB is a hepatitis B antigen.

The reaction mechanism of 2,4-di-tert-butylaniline hydrochloride is the alkylation of anilines with protonated tert-butyl chloride. This reaction proceeds by a substitution process in which one or more hydrogen atoms are replaced by the substituent. The selectivity of this reaction depends on the parameters and conditions used to carry it out. The reaction can be carried out under autogenous conditions or with the addition of a catalyst such as nickel (Ni), palladium (Pd) or platinum (Pt). The product obtained can be modified by changing the catalyst, solvent, temperature, pressure and other parameters. Reaction kinetics is affected by additives such as water, alcohols and acids that may be added during the reaction process. The size and shape of nanoparticles can also affect kinetic properties. 2,4-di-tert-Butylaniline hydrochloride has been shown to have high activity for organic synthesis in hom

2-Iodoaniline is a nucleophilic compound that reacts with electrophiles to form alkyl halides. It is used in the synthesis of β-aminoesters, which are used as γ-secretase inhibitors for the treatment of Alzheimer's disease. 2-Iodoaniline has been shown to be an effective inhibitor of protozoan parasites, such as Leishmania major and Trypanosoma cruzi, by blocking the conversion of pyruvate to oxaloacetate via enzymatic action. The chloride ion stabilizes the phenoxide anion intermediate and facilitates nucleophilic attack on the aromatic ring. 2-Iodoaniline has also been shown to be a competitive inhibitor of acylation reactions, due to its ability to bind covalently with acyl groups and inhibit their formation.

Please enquire for more information about 2-Fluoro-5-pivalamidobenzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Sulfabenzamide is a sulfa drug that has been used in the treatment of infectious diseases. It inhibits microbial growth by inhibiting synthesis of folic acid, which is essential for bacterial growth. Sulfabenzamide has been shown to have antimicrobial effects against a number of microorganisms, including several Gram-positive and Gram-negative bacteria. This drug also has anti-inflammatory properties and can be used in the treatment of bowel disease, such as ulcerative colitis. Sulfabenzamide is used to treat choroidal neovascularization in patients with age-related macular degeneration. This drug binds to glycol esters on the surface of human erythrocytes and can be extracted using dispersive solid-phase extraction (DSPE). The DSPE extract was analyzed by a LC-MS/MS method and found to contain sulfabenzamide and sulfadiazine.

4,5-Difluoro-2-methylaniline is a chemical intermediate that is used as a reaction component in the synthesis of organic compounds. It is a fine chemical with CAS No. 875664-57-6, and it can be used as a building block for the synthesis of complex organic molecules. This reagent is useful for the production of pharmaceuticals, agrochemicals, and other specialty chemicals. 4,5-Difluoro-2-methylaniline has been shown to act as an intermediate for the synthesis of many different types of compounds, including complex compounds such as imidazole derivatives and N-(4-fluorophenyl)benzo[d]oxazole derivatives.

2-Amino-5-chlorobenzamide is a fluorescence probe that has been shown to react with anthranilic acid, which is a structural component of many active substances. It is used in organic solvents as an indicator for the presence of active oxygen. 2-Amino-5-chlorobenzamide can be used as a linker to connect different molecules and can be activated by dehydrating agents, such as sodium sulfite. This compound has been demonstrated to have a linear response over a wide range of concentrations. The molecular target of 2-amino-5-chlorobenzamide is unknown at this time, but it has been suggested that it may interact with amino acids or proteins. The structural formula for 2-amino-5-chlorobenzamide is C6H4ClN2O2.

N,N-Diisobutyl-2-(octylphenylphosphoryl)acetamide is a redox active extractant that is used for the extraction of metals from acidic solutions. It has been shown to have an adsorption mechanism that includes hydrogen bonding and intramolecular hydrogen bonding. N,N-Diisobutyl-2-(octylphenylphosphoryl)acetamide also has a high redox potential and fluorescence properties. This extractant can be used as a metal chelate to extract copper from hydroxide or carbonate solutions. It can also be used in titration calorimetry experiments.

Please enquire for more information about 3-Chloro-4-fluoroaniline including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Bromo-2-chloroaniline (4BCA) is an exciplex that forms in the presence of hydrogen peroxide and chloride ions. It is unreactive with fluconazole and other related molecules, but is able to photoreduce hydrogen peroxide. The molecular mechanism of 4BCA is a result of its ability to form a covalent bond with DNA containing pyrimidine bases. This reaction results in the formation of pyrimidine dimers, which can lead to cell death through the inhibition of DNA synthesis and repair. 4BCA has been shown to be effective against cancer cells at high concentrations, but does not affect healthy cells. The effectiveness against cancer cells may be due to the fact that this exciplex reacts with uv irradiation and irradiation, which leads to a higher concentration of reactive oxygen species (ROS).

3,5-Dimethoxybenzamide belongs to the class of quinolone drugs. It is a potentiator of nabilone, which is a synthetic cannabinoid similar to THC. 3,5-Dimethoxybenzamide has been shown to be an electron-deficient compound that reacts with 5-hydroxytryptamine (serotonin) in vitro. This reaction leads to the formation of hydrogen bonds and modifications in the structure of serotonin molecules. 3,5-Dimethoxybenzamide also has grignard reagent activity and can be used as a carboxyamide or amide precursor in organic synthesis.

Aniline derivative; analgesic; anti-pyretic; electroosmotic flow marker

Aniline is an aromatic amine and is a clear to slightly yellow liquid with a characteristic odor. Aniline is an important precursor in the production of a wide range of industrial chemicals, including polyurethane foams, agricultural chemicals, and dyes. Aniline is also used in the manufacture of pharmaceuticals, rubber processing chemicals, and antioxidants. Due to its widespread industrial use, aniline can be found in various environmental matrices, including water, wastewater, and air.

2-Bromoaniline is a chemical compound that can be prepared by the acylation reaction of an amine with a bromoacetic acid. It has been used as an antimicrobial agent and as a growth factor in tissue culture. 2-Bromoaniline has been shown to inhibit the growth of multi-walled carbon nanotubes, which are known to cause toxicity to cells. 2-Bromoaniline has also been shown to have cytotoxic activity against epidermal growth factor receptor (EGFR) and natural compounds such as morphine, which may be due to its ability to bind with amines and diazonium salt.

5-Chloro-2-methylaniline is an organic compound that is a member of the amines class. It has been shown to be genotoxic and carcinogenic in vivo. 5-Chloro-2-methylaniline binds to DNA and inhibits the synthesis of RNA, leading to cell death. It is also toxic to aquatic organisms by inhibiting cellular respiration and causing mutations. 5-Chloro-2-methylaniline has been shown to be genotoxic in vitro and in vivo, with chronic oral toxicity observed at dietary concentrations of 0.1% (10 ppm) in animals. The toxicity of this compound may be due to its ability to form hydrogen chloride when mixed with water or other acids.

3-Amino-4-methoxybenzamide (3AMB) is a transcriptional regulator that inhibits the expression of genes encoding for the synthesis of aminoglycoside antibiotics. 3AMB binds to DNA, forming a heteromer with the transcription factor HANATX, which prevents RNA polymerase from binding to DNA. This in turn inhibits gene expression and bacterial growth. 3AMB has been shown to trigger diabetic neuropathy by inhibiting xylitol dehydrogenase, an enzyme required for neuron protection against oxidative stress. The drug also has a high affinity for nucleophiles and can bind to various substrates such as sulfhydryl groups or hydroxyl groups.

3-Methylbenzamide is an organic compound that belongs to the class of benzamides. It has been shown to cause a decrease in blood pressure and a decrease in viscosity, as well as an increase in blood flow to the testes. 3-Methylbenzamide has also been shown to inhibit the enzyme that catalyzes the conversion of tyrosine into dopamine and may be used for the treatment of Parkinson's disease with mild symptoms. The chemical ionization technique was used to study the binding of 3-methylbenzamide with rat plasma proteins and showed that this molecule binds with high affinity to albumin and alpha 1-acid glycoprotein. This binding was found to be reversible, which suggests that 3-methylbenzamide may not be metabolized by liver enzymes.

4-(1-Adamantyl)aniline is a monomer with electron-deficient properties. It can be synthesized from 1-adamantanol and trifluoroacetic acid, followed by hydrolysis to remove the trifluoromethyl group. 4-(1-Adamantyl)aniline has been shown to have high cytotoxicity against tumor cells in vitro. This compound also inhibits the production of necrosis factor, an inflammatory cytokine that plays an important role in many pathological processes, such as septic shock and acute respiratory distress syndrome.

3-Fluoro-4-methoxyaniline is a chemical intermediate. It is an aminopyridine that is used in the synthesis of bosutinib, an anticancer drug. 3-Fluoro-4-methoxyaniline binds to the ATP binding site of the cell's mitochondria and prevents the release of cytochrome c from the mitochondria, which leads to apoptosis. 3-Fluoro-4-methoxyaniline also has antimitotic effects and can inhibit the growth of tumor cells. 3-Fluoro-4-methoxyaniline has been shown to have poor cellular uptake, which may be due to its interaction with positron emission tomography (PET) agents such as cyanuric acid or glycopeptide. This chemical has also been shown to be a good surrogate for chloride ions in studies on transfected tumor cells.