Carboxylic Acids

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<p>2-(Chloromethyl)benzoic acid (CMBA) is a reactive chemical that can be used as an oxidant or a carbanion. CMBA is activated by sulfinyl, alicyclic, and sulfoxides, which are organic compounds with one or more sulfur atoms. These reactions may be either alkylation or condensation reactions. The activated CMBA can then react with chlorine to form chlorinated products. This reaction can be catalyzed by low energy sources, such as light or heat.</p>

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Medronic acid is a drug that is used for the treatment of chronic bowel disease. Medronic acid is a prodrug, which is converted to its active form, meclofenamic acid, by esterases in the bowel. Medronic acid has been shown to inhibit the activity of 5-lipoxygenase and cyclooxygenase-2 enzymes, and thereby reduce inflammation. It also decreases the production of prostaglandins and leukotrienes in humans. Medronic acid has been shown to be an effective treatment for bone cancer with no significant side effects. Medronic acid has been shown to inhibit the activity of 5-lipoxygenase and cyclooxygenase-2 enzymes, and thereby reduce inflammation. It also decreases the production of prostaglandins and leukotrienes in humans. Medronic acid has been shown to be an effective treatment for bone cancer with no significant side effects.

2,2,2-Trifluoroacetic acid 1-(2,4-dimethylphenyl)-2-[(3-methoxyphenyl)methylene]hydrazide is a neuroprotective drug that belongs to the class of hydrazides. It has been shown to have neurotrophic activity in vitro and in vivo and can be used for the treatment of conditions such as diabetic neuropathy or cancer tissues. 2,2,2-Trifluoroacetic acid 1-(2,4-dimethylphenyl)-2-[(3-methoxyphenyl)methylene]hydrazide also has anti-inflammatory properties and can be used for the treatment of autoimmune diseases. The drug's mechanism of action is not fully understood but is thought to involve monoamine neurotransmitters.

Comanic acid is an organic compound that is a derivative of pyridinium. It can be synthesized from acetyl chloride and pyridine by reaction with silver ions in the presence of ethyl esters. Comanic acid has been shown to have anticholinergic activity and inhibit prostatic hypertrophy in rats. It is metabolized to propantheline, which has been shown to be a molecule that binds to chemokine receptors, inhibiting chemotaxis of activated T lymphocytes.

Tert-butyl(8-anti)-3-azabicyclo[3.2.1]oct-8-ylcarbamate (tBAA) is a heterocycle that has been modified to enhance its pharmacokinetic properties. Tert-butyl(8-anti)-3-azabicyclo[3.2.1]oct-8-ylcarbamate was designed to be metabolically stable and have a high bioavailability and isosteric properties with phosphatidylinositol, which it uses as a substrate in the catalytic cycle. This modification also increased tBAA's stability in vivo, leading to an increase in efficacy. The covalent attachment of the phenyl ring on the tertiary amine nitrogen of tBAA provides additional protection against hepatic metabolism by CYP450 enzymes, making it more potent than other compounds with similar structures that are not covalently attached to the amine group.

<p>2-Bromo-5-methylbenzoic acid is an organic compound that can be synthesized in the laboratory. It is used as a starting material for synthesis of various quinazolinones, which are ionic liquid catalysts. 2-Bromo-5-methylbenzoic acid has also been shown to inhibit ethylene production from glycols and to act as a potential catalyst for the conversion of trifluoromethane into ionic liquids. The synthesis of 2-bromo-5-methylbenzoic acid is not well documented, but it can be made by reacting methyl bromide with benzaldehyde or acetone in the presence of sodium hydroxide or potassium hydroxide. This reaction produces bromobenzene, which reacts with phosphorus pentachloride to produce 2-bromo-5-methylbenzoic acid.</p>

<p>4-Bromobenzenesulfonic acid is a chemical used in the synthesis of organic molecules. It is an intermediate in the production of cyclopropylboronic acid, which is used as a building block in various organic syntheses. 4-Bromobenzenesulfonic acid can be prepared by reacting pyridine with acetic anhydride and then adding sodium carbonate to remove water. This reaction produces a molecule with two acid groups that are nucleophilic and can react with carboxylic acids to form esters. The yield for this reaction is high and it does not require any special equipment or conditions. This chemical is also used as a linker for other compounds during synthesis reactions, such as diazonium salts or dioxane. 4-Bromobenzenesulfonic acid reacts with triethylphosphite to give disulfides, which are important for protein structure.</p>

<p>Please enquire for more information about 4-(2-Hydroxyethyl)-1H-pyrrole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic acid, sodium salt (AITC-S) is a stilbene derivative with inhibitory properties. It has been shown to inhibit the uptake of camp in rat ventricular myocytes and caco-2 cells as well as the release of camp from rat renal proximal tubules. AITC-S also inhibits the transport of camp into the cells. The mechanism by which AITC-S inhibits uptake is not yet known, but it may be due to competition for a common carrier or an effect on intracellular metabolism. This compound has also been shown to have an acute ischemic protective effect on rats when administered before reperfusion following coronary artery occlusion.

4-Pyridazinecarboxylic acid is a salt that contains sodium. It is a white crystalline solid that is soluble in water, ethanol, and acetone. It has been shown to be effective against Leishmania species and Cryptococcus neoformans. 4-Pyridazinecarboxylic acid inhibits the growth of these fungi by binding to their cell membrane and inhibiting protein synthesis. 4-Pyridazinecarboxylic acid forms coordination complexes with metal ions that are involved in electron transfer reactions during the oxidative phosphorylation process. This leads to a decrease in ATP production and an increase in reactive oxygen species (ROS), which disrupts the function of macrophages and other phagocytic cells, leading to immunosuppression.

3,4-Dihydro-1H-isochromene-1-carboxylic acid is a pyridine derivative that has been used as an intermediate in the synthesis of other compounds. 3,4-Dihydro-1H-isochromene-1-carboxylic acid is a weak acid that can be prepared by the reaction of 3,4-dihydroisoquinoline with chloroform and hydrochloric acid. It is also synthesized from 1,4 benzodioxane and phenylacetic acid. This compound has been used to prepare amides, amidines, and ureas. 3,4-Dihydroisoquinoline is also used as a precursor for the synthesis of pyridinium salts.

<p>1-Benzyl-5-methyl-1H-1,2,3-triazole-4-carboxylic acid is a compound with an esterified hydroxyl group in the form of an acetylacetone. It can be used as a monohydrate or dihydrate and it is stabilized by hydrogen bonding. 1-Benzyl-5-methyl-1H-1,2,3-triazole-4-carboxylic acid has been studied as a potential drug for cancer treatment because it is active against tumor cells and has little toxicity to normal cells.</p>

Please enquire for more information about 15-Tritylmercapto-4,7,10,13-tetraoxapentadecanoic acid monohydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about Amoxicillin dimer tri-sodium salt (penicilloic acid form) - mixture of diastereomers including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>N-Succinimdyl-N-methylcarbamate is a reactive, antimicrobial agent that inhibits the activity of an enzyme in the cycle of cellular respiration. It binds to the active site of the enzyme, preventing it from functioning. N-Succinimdyl-N-methylcarbamate has been shown to inhibit hepatitis by inducing apoptosis. The drug has a phase transition temperature of approximately -6°C and is stable at higher temperatures. N-Succinimdyl-N-methylcarbamate has been shown to have an inhibitory effect on cyclic peptides, including those found in bacteria such as Helicobacter pylori and Chlamydia trachomatis.</p>

<p>15b-Hydroxy cyproterone acetate is a metabolite of cyproterone and cyproterone acetate, which are synthetic anti-androgens that inhibit the production of testosterone. This metabolite can be detected in urine as an inactive form or as an active form that binds to the androgen receptor. 15b-Hydroxy cyproterone acetate has been shown to cause tumours in monkeys.</p>

3-Isopropylisoxazole-5-carboxylic acid (3IPA) is an inhibitor of voltage-gated calcium channels. It has been shown to be effective in the treatment of neuropathic pain by reducing the excitability of neurons. 3IPA exhibits its analgesic properties through its binding to the t-type calcium channel, which is responsible for regulating the flow of calcium ions into cells. 3IPA also reduces neuronal excitability by inhibiting voltage-gated potassium channels and glutamate release. 3IPA may be a potential therapeutic agent for neuropathic pain, as it provides a novel approach to treating this type of pain.

<p>5-Oxo Rosuvastatin is a drug product that has been synthesized from natural ingredients. It is an analytical standard for the impurity, 5-oxo-rosuvastatin, which is a potential impurity in the API, rosuvastatin. This drug product has been custom synthesized in order to provide an Impurity Standard for HPLC. This drug product is also used as a Synthetic Reference Standard for Drug Development and Research and Development.</p>

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<p>3-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.</p>

Ethyl 6-methylpyridine-2-carboxylate is a pyridine derivative that has a nitrogen at the 6 position. It is an anionic compound, which is soluble in methanol and dichloromethane. The compound can be used to synthesize pharmaceuticals or as a precursor for polymers. It has been shown to inhibit the growth of tumor cells by binding to type 1 receptor sites on the surface of cancer cells. It also binds to quinine and enolate groups, which are found in many drugs. These binding sites may be exploited for drug design purposes.

<p>Please enquire for more information about Ethyl5-acetyloxy-1,2-dimethylindole-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Alpha-amino-2H-tetrazole-5-acetic acid (AAT) is a neurotoxin that inhibits glutamate receptors and causes neuronal cell death. It also decreases heart function in rats by inhibiting the cardiac sodium channel. AAT has been shown to be effective for inducing neuronal death in Xenopus oocytes, as well as decreasing the expression of certain receptor protein, such as NMDA and AMPA receptor subtypes. AAT is also known to cause apoptosis, which may be due to its inhibition of receptor function.

<p>Fluperolone acetate is a synthetic steroid that has been used as an anti-inflammatory agent. It is a potent corticosteroid and has been shown to inhibit the growth of microorganisms, such as bacteria and fungi. Fluperolone acetate does not cross the blood-brain barrier into the central nervous system, so it can be used for the treatment of inflammatory diseases in the eye without affecting vision. This drug also has been shown to reduce choroidal neovascularization in patients with age-related macular degeneration. Some biodegradable implants have been made from fluoropolymers, which are biocompatible polymers that are degraded by hydrolysis or enzymatic action in vivo. These implants may provide a sealant for use in surgical procedures and for treating cavities.</p>

<p>1,1'-Bicyclo[1,1,1]pentane-1,3-dicarboxylic acid monomethyl ester is a chemical compound used in research and as a building block for complex compounds. It is a high quality and versatile compound that has a wide range of uses in the production of fine chemicals. This compound is an intermediate for the synthesis of 1,4-benzodioxan. CAS No. 83249-10-9</p>

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<p>Ethyl 2-ethylacetoacetate is a carbonyl compound that belongs to the supramolecular class of chromenones. The molecule has an x-ray diffraction pattern that is characteristic of a ring structure. It can be synthesized by an efficient method involving the reaction of ethyl benzoylacetate with a halide in the presence of acid catalyst. The reactants are isolated in high yield and structural analysis shows the presence of a methylene group and an ethyl group on opposite sides of the ring, which are bonded to each other through an acetoacetate group. This chromenone also displays photochemical properties and can be used as a substrate for functional theory studies.</p>

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<p>Ethyl 1,2-dimethyl-5-hydroxyindole-3-carboxylate (EDMC) is an implantable drug that is used to treat hypertension. It is a diuretic that can be taken orally or injected. EDMC works by reducing the amount of urea nitrogen in the blood and increasing the amount of chlorine atom in the urine. This leads to an increase in active substances such as malonic acid and a decrease in arthropoda. EDMC has been shown to have antihypertensive activity due to its ability to lower diastolic and systolic pressure. The molecule also contains hydroxyl group and aldehyde groups that are analyzed by analytical chemistry.</p>

<p>N10-Methyl pteroic acid is a novel immunosuppressant that inhibits T-cell proliferation and promotes regression of inflammatory bowel disease. It has been shown to be effective in treating cancer patients, with the terminal half-life being approximately 20 hours. N10-Methyl pteroic acid is a potent inhibitor of human acute lymphoblastic leukemia cells. It can also be used as an immunosuppressant for organ transplantation, with desorption from gels using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF MS) and bioanalytical methods such as high performance liquid chromatography (HPLC).</p>

<p>1,3,5-Naphthalene trisulfonic acid is an organic compound that is the product of the sulfonation of naphthalene. It has been shown to inhibit the activity of 3β-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase, enzymes involved in steroidogenesis. The maximal response was observed at a concentration of 500 μM with a detection time of 30 minutes. Xenopus oocytes were used for expression and chloride currents were recorded as an indicator for enzyme activity. Concentration-response curves were generated with organic solvents such as methanol and dimethyl sulfoxide (DMSO). 1,3,5-Naphthalene trisulfonic acid also inhibits the oxidative activities of some enzymes such as lipoxygenase and cyclooxygenase.</p>

3-Aminopicolinic acid is a carboxylate that can be found in the cytosol, mitochondria, and nucleus of cells. It is an efficient method for the synthesis of picolinic acid from 3-aminopyridine-2-carboxylic acid. The synthesis of picolinic acid has been shown to have structural analogs to molecules involved in nucleotide metabolism such as single-stranded DNA, mitochondrial DNA, and mitochondrial RNA. 3-Aminopicolinic acid has been shown to increase renal blood flow by stabilizing complexes with chloride and phosphoenolpyruvate. This compound also enhances the renal excretion of picolinic acid. 3-Desacetylcefotaxime potassium Tilmicosin Gatifloxacin 3-Aminopicolinic acid

<p>Ethyl bromodifluoroacetate is a chemical substance that reacts with amines in the presence of copper to form a copper complex. It is used as an intermediate in the synthesis of organic compounds, such as pharmaceuticals. Ethyl bromodifluoroacetate is also used as a catalyst for cross-coupling reactions of organic molecules. This reaction requires low energy and can be performed under mild conditions. The asymmetric synthesis of ethyl bromodifluoroacetate requires few steps and only uses inexpensive starting materials. The carbonyl group is chemically stable, making it difficult to decompose or oxidize. However, hydrogen fluoride will react with ethyl bromodifluoroacetate and cause it to decompose into its elements, fluorine and carbon dioxide gas. In addition, nucleophilic attack by halides can lead to the formation of ethyl bromodifluoroacetate from other substances. Control agents are necessary</p>

E-Hexen-1-ylboronic acid is a reactive, boron-containing compound that can be used for Suzuki coupling reactions and metathesis reactions. It is also useful in the analysis of organic compounds, due to its ability to form brightly coloured complexes with metal ions. E-Hexen-1-ylboronic acid has been shown to react with chloride, reoxidant and hexane. This compound can be used as an analytical reagent for the detection of stereoselectively in a stepwise reaction. E-Hexen-1-ylboronic acid forms crystals x-ray diffraction patterns that are characteristic of a chair conformation.

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5-bromo-3-methylthiophene-2-carboxylic acid (5BmtCA) is a potential therapeutic that has been shown to have the same estrogenic activity as estradiol. It may be used for the treatment of osteoporosis and other conditions associated with estrogen deficiency, including resorption and bone loss. 5BmtCA is an amide with two phenyl groups at the C3 position, which are bioisosteres of the sulfur in estradiol. The substitutions on these phenyl groups can be changed to produce analogs with different properties. For example, 5BmtCA may be substituted with a ketone group at position C3 to produce the corresponding ketone analog 5BmtCK. This compound would be expected to have reduced bone resorption activity relative to 5BmtCA.

5-(4-Fluorophenyl)-3-isoxazolecarboxylic acid is a high quality reagent with CAS No. 33282-24-5. It is a complex compound that is useful as an intermediate for the synthesis of various fine chemicals. 5-(4-Fluorophenyl)-3-isoxazolecarboxylic acid also has a number of uses in the synthesis of speciality chemicals, research chemicals, and versatile building blocks for organic chemistry. As a reaction component, it can be used to synthesize compounds with different functional groups on their molecules.

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<p>Benzoic acid 1-(4-hydroxybutyl) ester is a metabolite of benzenedicarboxylic acid, which is the active ingredient in some insecticides. Benzoic acid 1-(4-hydroxybutyl) ester is found in amniotic fluid and maternal urine. It is a toxicant to the fetus and can cause severe neurological damage if ingested by a pregnant woman. The toxicological effects are due to its ability to inhibit the synthesis of proteins necessary for cell division and growth, as well as its ability to induce oxidative stress.</p>

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