Ácidos Benzóicos

2-Iodobenzoic acid is a synthetic compound that is used in the treatment of wastewater. It is produced by the reaction of benzoate and nitrite in the presence of sodium hydroxide. The intramolecular hydrogen atom transfer from the 2-iodobenzoic acid to benzoate is a reversible reaction. This process can be catalyzed by palladium, which has been shown to be effective in coupling 2-iodobenzoic acid with other compounds to produce cyclic peptides. The use of 2-iodobenzoic acid as a contraceptive has been investigated for its ability to inhibit acetylcholinesterase activity, which may lead to increased levels of acetylcholine and inhibition of muscle contractions.

4-Hydrazinobenzoic acid hydrochloride is a chemical species that has an oxidative effect on DNA. It is a reactive oxygen species (ROS) that changes the hydrogen spectrum of water. The hydrogen bond is broken and the electrons in the molecule are excited to a higher energy level, which results in ROS formation. 4-Hydrazinobenzoic acid hydrochloride also inhibits mitochondrial function and causes heart disease by increasing blood pressure and weakening the heart muscle. This compound can be used as a cancer treatment for human cells, because it suppresses genes that promote cell growth. In addition, 4-hydrazinobenzoic acid hydrochloride may inhibit endothelial cell proliferation in animal experiments.

Ethyl 4-nitrobenzoate is a compound that is used to synthesize other drugs, such as erythromycin. It is also an intermediate in the synthesis of some pesticides and dyes. The second-order rate constant for the reaction of ethyl 4-nitrobenzoate with phosphotungstic acid has been measured at 0.058/min at 25°C. This reaction is catalyzed by recombinant cytochrome P450 (P450) enzymes from human liver preparations and cationic surfactants such as nitrobenzene or sodium carbonate, which are known to form hydrogen bonds with the protonated nitrogen atom on the aromatic ring of ethyl 4-nitrobenzoate. Ethyl 4-nitrobenzoate is also used clinically to treat gastric ulcers, although it can be toxic if taken in large doses or over a long period of time.

Ethyl 3,5-dichloro-4-methoxybenzoate is an organic compound that has a variety of uses. It is an intermediate in the synthesis of various other compounds and as a reagent, it reacts with amines to form ureas. Ethyl 3,5-dichloro-4-methoxybenzoate can also be used as a complex building block for synthesizing other compounds. This chemical can be used as a speciality chemical or research chemical. As a versatile building block, ethyl 3,5-dichloro-4-methoxybenzoate can be used to make reaction components for synthesizing polymers or pharmaceuticals.

5-Amino-2-chlorobenzoic acid is a carboxylate that has antiproliferative effects. It is synthesized through the reaction of morpholine and malonic acid. 5-Amino-2-chlorobenzoic acid has been shown to have an optimal reaction with UV light, which may be due to its structure activity relationship with other carboxylates. It also has a high affinity for metal ions such as magnesium and chloride, which are thought to be important in cancer cell proliferation. 5-Amino-2-chlorobenzoic acid can be used in analytical methods because it is soluble in water and can be obtained through gravimetric analysis.

4-Vinylbenzoic acid is a water-insoluble polymer that has been shown to have bacteriostatic and fungistatic properties. 4-Vinylbenzoic acid inhibits bacterial growth by binding to the enzyme diphenolase, which is involved in the synthesis of cell wall precursors. This polymer also binds to cationic surfactants and is soluble in organic solvents such as ethanol and acetone. The mechanism of inhibition of fungal growth is not known, but it may be due to hydrogen bonding interactions with the cell membrane.
4-Vinylbenzoic acid has been shown to be effective against human serum, although it does not inhibit bacterial growth in this medium.

3-Amino-2-chlorobenzoic acid is a molecule that belongs to the group of acidic compounds. It has been shown to induce apoptosis and inhibit cell proliferation in human immunodeficient virus (HIV) cells, as well as inhibit the growth of cancer cells. 3-Amino-2-chlorobenzoic acid also inhibits histone deacetylase, which is an enzyme that controls gene expression by removing acetyl groups from lysine residues on the N-terminal tails of histones. This inhibition may be responsible for its anticancer activity. 3-Amino-2-chlorobenzoic acid is metabolized by oxidation to chlorinated derivatives and excreted via the kidneys. It has been shown to have a pharmacokinetic profile in rats similar to that observed with other triazines such as atrazine and simazine. The elimination half-life of 3-amino-2-chlorob

Organic anion transporter inhibitor; pannexin 1 channel inhibitor

4-Chloro-2-fluorophenyl)acetic acid ethyl ester is a fine chemical that can be used as a scaffold for building more complex molecules, or it can be used as a versatile building block in the synthesis of research chemicals. It is also an intermediate in many reactions and can be used as a speciality chemical. 4-Chloro-2-fluorophenyl)acetic acid ethyl ester has been shown to have high quality and it is useful for research on complex compounds. It can also be used as a reagent in organic synthesis.

4-(Acetylamino)-2-nitrobenzoic acid (AAANB) is a versatile building block that can be used in the synthesis of a wide range of organic and pharmaceutical compounds. AAANB is an intermediate in the preparation of 4-Amino-3-nitrophenol, which is an important research chemical. This compound is a useful scaffold for the synthesis of organic compounds with various biological activities. The CAS number for this product is 21573-29-5.