Organic Halides

Please enquire for more information about 6-Bromo-3-phenylquinazoline-2,4(1H,3H)-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

Lauroylcholine chloride hydrate is a chemical compound that has been shown to have antimicrobial activity. It has been shown to react with exogenous acceptors such as pluronic F127, benzalkonium chloride, and inorganic acid. The reaction mechanism of Lauroylcholine chloride hydrate is not well understood, but it is thought to be due to the presence of a hydroxyl group and a carbonyl group on the molecule. Lauroylcholine chloride hydrate is a non-polymeric cationic surfactant with molecular weight similar to heparin's. This chemical compound may be used as an additive in personal care products or pharmaceuticals.

<p>Please enquire for more information about 4-Benzyl-piperazine-1-carbonylchloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

2-Dimethylaminoisopropyl chloride hydrochloride is a fluorescent molecule that emits light at wavelengths of 370-430 nm. It has a number of uses, such as detecting the presence or absence of chloride ions in water samples, determining the composition of petroleum products, and measuring the concentration of sodium ions in electrolytes. 2-Dimethylamino-1-propanesulfonic acid chloride hydrochloride can be used to identify the transition metal (Cu) in a sample, because it absorbs light at wavelengths below 450 nm.

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<p>1-Bromo-5-chloro-2-fluorobenzene is an antibacterial and antifungal agent that belongs to the group of halogenated brominated compounds. It has shown effective inhibitory activity against a wide range of bacteria, including Staphylococcus aureus and gram-negative bacteria. 1-Bromo-5-chloro-2-fluorobenzene has been used as a treatment for small ulcers in the mouth caused by fungi. The drug inhibits bacterial growth by interfering with the synthesis of protein, DNA, and RNA. 1-Bromo-5-chloro-2-fluorobenzene also inhibits the growth of fungi by inhibiting their production of ergosterol, which is necessary for cell membrane function.</p>

<p>3-Bromoacetylpyridine, hydrobromide is a derivatizing agent that has been shown to react with nucleophiles. It can be used as an electron donor or electron acceptor in radical scavenging and other reactions. 3-Bromoacetylpyridine, hydrobromide is also a ligand for metal ions, and has been shown to bind to copper(II) ions. This product ionizes easily under electrospray ionization and reacts with thiourea to form 3-acetylpyridine.</p>

<p>Please enquire for more information about 1,1,1-Trichloro-3-(1-methyl-1H-benzimidazol-2-yl)propan-2-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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5-Chloro-2,2-difluoro-1,3-benzodioxole (5CFD) is an antifungal agent that is used to treat bowel disease. It inhibits the synthesis of DNA and RNA by binding to the enzyme RNA polymerase. 5CFD is also used as a precursor for diazonium salt analogs, which are used in antibacterial agents. The analogs are synthesized using deuterated 5CFD. This drug has been shown to have antitumor activity against human cervical carcinoma cells in culture.

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<p>2,4-Dinitrobenzenesulfonyl chloride is a chemical reagent that is used in analytical chemistry. It reacts with pyrazole rings to form 2-aminopyridine derivatives. The reaction can be enhanced by adding metal ions such as copper(II) or zinc(II). 2,4-Dinitrobenzenesulfonyl chloride is also used in the solid-phase synthesis of heterocycles and in the synthesis of pharmaceuticals. The compound has been shown to react with human serum and form an unstable intermediate that undergoes hydrolysis to produce sulfate ion and trifluoroacetic acid. This reaction mechanism can be applied to other nucleophilic compounds such as bromide ion. 2,4-Dinitrobenzenesulfonyl chloride reacts with the amine group of proteins using the S N 1 mechanism. The resulting product is a chlorinated amino acid derivative which exhibits fluorescence properties when reacted with</p>

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<p>2-(Trifluoromethoxy)benzyl bromide is a computational study of ionic liquids with substitutions. The viscosity of the liquid was found to be dependent on the size of the substituent and the number of substitutions. The compound was found to be selective for one isomer over another due to its different structural features. Experimental studies have shown that 2-(trifluoromethoxy)benzyl bromide has high permeability in ionic liquids, which is a desired property in ionic liquids. Advances in this field have led to new compounds and more knowledge about the properties of ionic liquids.</p>

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7-Phenylacetamide-3-chloromethyl-3-cephem-4-carboxylic acid diphenylmethyl ester is an organic solution that is used in the detoxification of chemical substances. It has a hydroxyl group and is soluble in nonpolar solvents. 7PAMC has been shown to be effective against bone lesions caused by acylation reactions. This drug also binds to the enzyme called cytochrome P450, which is involved in the metabolism of many drugs. It also inhibits bacterial growth by binding to DNA gyrase and topoisomerase IV, enzymes that maintain bacterial DNA integrity. The particle size of this drug is small, with a diameter of less than 10 microns. 7PAMC has a viscosity of 1 cps at 25°C and a melting point of 129°C.

<p>Cyclopropyl 2-fluorobenzyl ketone is an inhibitor that blocks the production of cyclic nucleotides and thereby inhibits the activity of the enzyme phosphodiesterase. It has been shown to inhibit platelets and inhibit the metabolic rate in rats. The drug also has a cytotoxic effect on rat liver cells, which may be due to its ability to bind hydrogen bonds. Cyclopropyl 2-fluorobenzyl ketone has been found to have a strong inhibitory effect on ticagrelor, statins, and anti-platelet agents. This drug has also shown a potential for adverse drug interactions with other biological products such as erythropoietin, insulin, or heparin.</p>

<p>Dichlorodiisopropylsilane is a cycloaddition process, which is the addition of two molecules to create a new ring. It reacts with an unsaturated organic compound, such as an alkene or alkyne, to produce a reactive functional group. Dichlorodiisopropylsilane has been used in chemistry as a cross-linking agent for proteins and as a solid catalyst. The chemical stability of dichlorodiisopropylsilane makes it useful in the synthesis of model proteins. This compound also has low bioavailability due to its high reactivity with hydrochloric acid found in the stomach.</p>

Please enquire for more information about [3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3-carboxylate is a chemical compound that has been shown to have anti viral activity in vitro. The structure of the compound suggests that it may inhibit the production of inflammatory cytokines. This drug inhibits the activity of enzymes such as hydroxylases and lipases, which are important for the inflammatory process. Ethyl 5-acetoxy-6-bromo-2-(bromomethyl)-1-methyl-1H-indole-3 carboxylate may be an effective treatment for bowel disease and other inflammatory conditions.

<p>Valethamate bromide is a pharmaceutical drug that is used as a neuroprotective agent. It is believed to be involved in memory, learning, and motor control. Valethamate bromide has been shown to statistically improve the clinical response of women with Alzheimer's disease. However, it does not have any effect on people without Alzheimer's disease. The molecular weight of this compound is 220.24 g/mol and its chemical formula is C14H17BrNO2. Valethamate bromide has been shown to produce an average particle diameter of 3 microns when analyzed by chromatography.</p>

<p>2,6-Dibromoanthracene is an aromatic hydrocarbon that can be synthesized in a cross-coupling reaction. It has been shown to have a high electron mobility and good thermal stability. The compound was prepared by the Suzuki coupling reaction of 2,6-dibromobenzene with phenylboronic acid. This product has no commercial use but has been tested for its transport properties and has been found to be activated by heat.</p>

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3,3-Difluoropentanedioic Acid is a reagent that is used in organic chemistry. It can be hydrolyzed to give 3,3-difluoro-1,2-propanediol. This chemical reacts with dithianes to give 1,2-dithiane and quantitatively produces 3-fluoro-1,2-propanediol. It is an ester of 3,3-difluoropentanedioic acid and has been shown to have antiinflammatory properties in rats.

8-Chlorotheophylline is a chemical compound used in pharmaceutical preparations as an antispasmodic and bronchodilator. It is a derivative of theophylline and has been shown to bind to receptors in the brain, lungs, heart, and smooth muscles. 8-Chlorotheophylline has been shown to have broad-spectrum antimicrobial activity against both Gram-positive and Gram-negative bacteria. The compound is water soluble at physiological pH levels and does not require a buffer for stability. This agent can be prepared by using a sample preparation procedure that includes adding sodium carbonate followed by caffeine to extract the sample from a biological matrix such as tissue or blood. 8-Chlorotheophylline can be analyzed by chromatography with UV detection (254 nm) or fluorescence detection (365 nm).

4-Fluorobenzoyl chloride is a chemical compound with the molecular formula of C6H4ClF. It is a colorless, volatile liquid that is soluble in water and most organic solvents. 4-Fluorobenzoyl chloride has been shown to have antimicrobial properties against bacteria such as methicillin resistant Staphylococcus aureus (MRSA). It also has antiinflammatory properties and can be used as an analgesic. The phase transition temperature of 4-fluorobenzoyl chloride is -72 degrees Celsius. The analytical method for this compound involves gas chromatography with mass spectrometry detection (GCMS). The receptor binding affinity of 4-fluorobenzoyl chloride is not known.

Please enquire for more information about Bupropion hydrochloride related compound B including the price, delivery time and more detailed product information at the technical inquiry form on this page

Bis(benzonitrile)palladium(II) chloride is a palladium complex with the coordination geometry of square-planar. It has been shown to undergo a suzuki coupling reaction when reacted with an aromatic hydrocarbon, such as benzene or toluene, in the presence of sodium carbonate and nitrogen gas. This reaction produces an intramolecular hydrogen bond between the oxygen atom of the hydroxyl group and the nitrogen atom on the chelate ligand. Bis(benzonitrile)palladium(II) chloride has also been shown to be useful for generating x-ray crystal structures of metal complexes by using ft-ir spectroscopy. The chlorine atom from bis(benzonitrile)palladium(II) chloride may react with hydrochloric acid to produce a soluble complex that can be isolated by crystallography.

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Ethyl 7-aminoheptanoate hydrochloride is an antibiotic that belongs to the class of esters. It has been shown to inhibit the growth of bacteria in vitro, which is attributed to its ability to inhibit protein synthesis. This drug has been used as a chemical manipulator in animal experiments. Ethyl 7-aminoheptanoate hydrochloride binds to the ribosomal RNA of bacteria and prevents amino acid incorporation into proteins, which leads to cell death. The endpoint of this experiment was determined by counting the number of rotations on a rotator after treatment with ethyl 7-aminoheptanoate hydrochloride or saline solution. Treatment with ethyl 7-aminoheptanoate hydrochloride resulted in an increase in the number of rotations, which is indicative of bacterial death.

Please enquire for more information about N,N-Didesmethyl diltiazem hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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3-Iodobenzoic acid methyl ester is a synthetic selenium compound that is used in the synthesis of fatty acids. It is also used as a radionuclide in the diagnosis of cancer and other diseases. 3-Iodobenzoic acid methyl ester can be taken orally or injected, but it should not be taken by pregnant women or those who are allergic to iodine. This product has been shown to have anti-cancer properties when given orally, although there are some potential side effects associated with usage. These side effects include nausea, vomiting, diarrhea, and an increase in urine production. 3-Iodobenzoic acid methyl ester is metabolized into toxic products such as biphenyl, which may cause an escalation of symptoms. The structural formula for this product is C8H7INOS2O2.

<p>7-Amino-4-(trifluoromethyl)coumarin is a coumarin derivative that has been used as a fluorescence probe for the study of enzyme activities. It can be used as a potential biomarker for autoimmune diseases, and has also been shown to have tyrosine kinase domain binding activity. 7-Amino-4-(trifluoromethyl)coumarin can bind to the hydroxyl group in tyrosine residues with high affinity, and binds to the nitrogen atoms in protein kinases with low affinity. This compound is able to form intermolecular hydrogen bonds and steric interactions with peptide hormones.</p>

2-(2-Chlorophenyl)ethylamine is an amine that inhibits the production of proteins vital for cell division. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 2-(2-Chlorophenyl)ethylamine has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. 2-(2-Chlorophenyl)ethylamine has shown anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.

<p>S-Aminoethyl-L-cysteine hydrochloride is an amino acid that is used in the diagnosis of metabolic disorders. It has been found to have a high concentration in plasma and can be used to measure the activity of bowel disease. S-Aminoethyl-L-cysteine hydrochloride is also used as a diagnostic marker for inflammatory diseases. It is extensively metabolized by acidic hydrolysis, which results in the release of chloride ions and amines.</p>

<p>Cyclobutanecarboxylic acid chloride is an acyl halide that is a reactive chemical intermediate. Cyclobutanecarboxylic acid chloride reacts with naphthalene to produce cyclobutane, which can undergo a Friedel-Crafts reaction to form a benzene ring. The compound also has been shown to inhibit the growth of human cervical carcinoma cells by inhibiting the production of growth factors and interferon, as well as by inducing apoptosis. Cyclobutanecarboxylic acid chloride has been used in the treatment of infectious diseases such as tuberculosis, leprosy, and malaria. This drug was originally synthesized for use as a protein inhibitor, but it has not been found to be active in this application.</p>

<p>5-Bromo-6-methylpyrimidine-2,4(1H,3H)-dione is an immunosuppressive drug that belongs to the class of hydantoins. It can be used to treat a variety of diseases associated with immunodeficiency including AIDS. 5-Bromo-6-methylpyrimidine-2,4(1H,3H)-dione inhibits viral replication by alkylating nucleotides and DNA synthesis at the GTPase level. The amide group in the molecule is responsible for this property. Kinetics studies have shown that the rate of hydrolysis of 5-bromo-6-methylpyrimidine-2,4(1H,3H)-dione depends on the pH and temperature of solution.</p>

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<p>Chlorpromazine is a phenothiazine antipsychotic drug that is used to treat schizophrenia and other mental disorders. It is also used in the treatment of nausea, vomiting, and hiccups. Chlorpromazine binds to the D2 receptor in the brain, which blocks dopamine from binding to this receptor. In addition to its effects on dopamine receptors, chlorpromazine also inhibits phosphodiesterase activity and n-oxide formation. These effects are thought to be responsible for chlorpromazine's ability to inhibit tumor growth and prolong survival in some cancer patients. Chlorpromazine has been shown to inhibit filamentous fungi by inhibiting kinesin-like proteins that are essential for cell division. This drug also has low potency against cyclic nucleotide phosphodiesterases (PDEs) and may act as an inhibitor of PDE4B1 which is involved in the inflammatory response.</p>

<p>Please enquire for more information about [1-(4-Chlorobenzyl)-1H-benzimidazol-2-yl]methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 3-Bromo-N,N-dimethylpropan-1-amine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (7a,17beta)-7-(9-Bromononyl)estra-1,3,5(10)-triene-3,17-diol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Dichloro-4-methoxybenzoic acid is a synthetic herbicide that inhibits the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS). This enzyme is necessary for the synthesis of aromatic amino acids. 2,5-Dichloro-4-methoxybenzoic acid is used as a selective herbicide in plants grown in vitro to eliminate weeds. It is also used to control populations of wild plants and grasses. 2,5-Dichloro-4-methoxybenzoic acid has been shown to inhibit the growth of glyphosate resistant weed species by inhibiting EPSPS activity.</p>

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3-Bromopyridine is a colorless liquid that is soluble in water and methanol. It has a chemical ionization mass spectrum with hydrogen bonding interactions, which are shown by the nitrogen atoms. 3-Bromopyridine reacts with amines to form nitroso compounds and has transport properties that are dependent on pH. 3-Bromopyridine has been shown to be a metastable substance, which means it can be isolated in a yield of greater than 50%. 3-Bromopyridine is soluble in alkaline solutions, but decomposes at high temperatures. The solution turns red when phosphotungstic acid is added and it gives an orange precipitate when hydrochloric acid is added. The solution turns yellow when sodium hydroxide is added. 3-Bromopyridine can be detected by its nmr spectra and kinetic energy measurements.

3-Nitro-4-chloro-benzotrifluoride is a nucleophilic reagent that reacts with aryl chlorides, such as phenoxazine and chloride, to give the corresponding nitro compounds. The reaction yield is dependent on the solvent, with higher yields obtained in n-dimethyl formamide than in dichloromethane. 3-Nitro-4-chloro-benzotrifluoride has been investigated for its potential use in cancer therapy. It inhibits the proliferation of a number of cancer cells, including resistant mutants. The deuterium isotope effect has also been used to determine the mechanism of action of 3-nitro-4-chloro benzo trifluoride.

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