Halogénures organiques

Anti-cancer alkylating agent; inhibits protein, RNA and DNA synthesis

Tris(4-bromophenyl)amine is a chemical compound that is used as an intermediate in the synthesis of other compounds. It has been studied for its electrochemical properties, which include its stability and ability to react with ethyl diazoacetate. The reaction mechanism of tris(4-bromophenyl)amine has been studied using electrochemical techniques, including kinetic and spectroscopic studies. Tris(4-bromophenyl)amine reacts with acid to produce nitrite ions and bromine water, which can then react with ethyl diazoacetate to produce aryl diazonium salts such as 3-nitrophenol. This process can be repeated multiple times to form aryl diazonium salts such as 6-nitrophenol or 5-nitrophenol. The electron reduction potential of tris(4-bromophenyl)amine is low enough that it can be easily oxid

2-Chloro-4,6-diphenyl-1,3,5-triazine is a linker that can be activated to accept an electron from a donor molecule. It is often used as a transport material in organic light emitting diodes (OLEDs) and organic photovoltaics (OPVs). 2-Chloro-4,6-diphenyl-1,3,5-triazine has been shown to have high efficiencies when it is thermally activated. This compound also has high efficiency when it is activated by light with a wavelength of 400 nm. The luminescent properties of 2-Chloro-4,6-diphenyl-1,3,5 - triazine are due to its electron deficient nature and the presence of methoxy groups.

1-Adamantyl(amino)acetic acid hydrochloride is an organic compound that is used as a versatile building block and intermediate in the synthesis of complex compounds. It reacts with nitric acid to form 1-Adamantyl nitrate, which is a useful reagent for organic synthesis. This compound has CAS number 16091-96-6 and can be found on the list of speciality chemicals. It is a fine chemical with high quality and is useful for research purposes.

5,7-Dichloro-1H-imidazo[4,5-b]pyridine is a synthetic compound that has been shown to inhibit the replication of herpes simplex virus in cell culture. It is active against a broad range of viruses including HIV and influenza A. The antiviral potency of 5,7-dichloro-1H-imidazo[4,5-b]pyridine against herpes simplex virus may be due to its ability to act as an agonist on adenosine receptor subtypes such as A2aR. This drug also has immunosuppressive properties and can be used for the treatment of immunodeficiency disorders.

6-Fluorosalicylaldehyde is a sulfate that has been used in the synthesis of 6-fluorosalicylic acid, which is an intermediate for the production of aspirin. It also can be used to synthesize phenols and formylation products. The reaction with hydroxylamine leads to salicylaldehydes, while the reaction with methoxide leads to salicylaldehyde.
6-Fluorosalicylaldehyde reacts with magnesium salts in acidic conditions to produce paraformaldehyde. Deprotonation of 6-fluorosalicylaldehyde yields methoxide.

2-Iodo-N-methyl-N-p-tolylbenzamide is a fine chemical that has the CAS No. 1387529-49-8 and is a versatile building block with a wide range of applications, including research chemicals, reaction components and speciality chemicals. 2-Iodo-N-methyl-N-p-tolylbenzamide is soluble in organic solvents such as ethers, chloroform and benzene, while insoluble in water. It has been shown to be a useful intermediate for the synthesis of complex compounds and can be used as a reagent to prepare other compounds. 2Iodo-Nmethyl--Np--tolylbenzamide has been shown to have high quality and is an excellent building block for synthesizing pharmaceuticals.

1-(2-Bromophenyl)-2-nitroethene is a chiral, enantioselective nitroalkene that is used in the synthesis of many biologically active compounds. The compound was found to be an effective chiral ligand for asymmetric reactions involving aldehydes, indoles, and bipyridine. It has been shown to be more reactive than other bromoalkyltin reagents and can be used in a variety of reactions. 1-(2-Bromophenyl)-2-nitroethene also has conformationally rigid skeletons, which may allow for higher yields when compared with other alkylation agents.

3-Fluoro-4-(trifluoromethyl)benzonitrile is a chemical compound with biological activity. It is structurally related to anthelmintics, and has been shown to be nematocidal in laboratory experiments. 3-Fluoro-4-(trifluoromethyl)benzonitrile has not been evaluated for safety or efficacy in humans.
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2-Bromo-5-fluorobenzyl alcohol is a synthetic organoboron compound that can be used in the synthesis of other compounds. It has been shown to have a thermal expansion coefficient of 0.038 x 10^-6 K, which is an intermediate value for organic materials. The two polymorphic forms are monoclinic (space group P2/c) and hexagonal (P63). When 2-bromo-5-fluorobenzyl alcohol is irradiated with microwaves and magnetic fields, it undergoes anisotropic expansion, which suggests that intermolecular interactions are important in this phenomenon. This material has been shown to exhibit antifungal properties.

L-Leucine ethyl ester hydrochloride (L-LEE) is a hydroxylated form of leucine, which is an essential amino acid. LEE has been shown to have anti-inflammatory effects, which may be due to its ability to inhibit the formation of proinflammatory cytokines. It also has been shown to have antioxidant and anti-atherogenic properties, as well as the ability to reduce cholesterol levels in rats. This product has been shown effective in treating bowel disease and metabolic disorders such as hepatic steatosis, fatty liver disease, and metabolic syndrome. LEE also can activate aryl hydrocarbon receptor ligand (AhR), which is involved in the regulation of genes that control inflammation and immune responses.

DL-alpha-Methylhistidine dihydrochloride is a reagent that has been used as a complex building block. It is an intermediate in the preparation of other compounds and is also used as a speciality chemical. DL-alpha-Methylhistidine dihydrochloride can be used to synthesize a variety of useful compounds, including pharmaceuticals, agrochemicals, and research chemicals. DL-alpha-Methylhistidine dihydrochloride can also be used as a versatile building block for the synthesis of other fine chemicals.

5-Iodocytosine (5-IC) is an analog of cytosine that can be used as a precursor for the synthesis of thymine. 5-IC has been shown to cross-couple with DNA, which may contribute to its antiviral potency. 5-IC is also a potent inhibitor of dna replication and herpes simplex virus. The biochemical properties of 5-IC have been extensively studied, including its ability to react with hydrochloric acid to form the corresponding tautomers. The hydrolysis rate increases at higher pH values and decreases at lower pH values. Bioconjugate chemistry has been applied to synthesize a bioconjugated prodrug of 5-IC for cancer treatment.

2,4-Dichlorobenzoic acid is a chemical compound that is commonly used for sample preparation for analytical methods. It is also used as a nutrient in group P2 bacteria. 2,4-Dichlorobenzoic acid has coordination geometry of octahedral with the central atom being surrounded by six ligands. This chemical has hydrogen bonding interactions that are most likely due to the electronegative chlorine atoms.

Acetyl L-carnitine chloride (ALCAR) is a carnitine molecule that is used as a dietary supplement. It can be converted to acetyl coenzyme A, which provides energy for the cells and helps with the production of neurotransmitters. ALCAR has been shown to reduce neuronal death in an animal model of oxidative injury. It also increases levels of glutathione and prevents lipid peroxidation. Acetyl L-carnitine chloride is a cell permeable reagent that can be used to measure GSH-px activities in biological samples. This compound has been shown to inhibit the activity of cell nuclei and mitochondrial enzymes, such as succinate dehydrogenase, citrate synthase, and malate dehydrogenase.

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4-Ethyl-1,3-thiazol-2-amine is a tertiary amine that is used as an alkylating agent. It has been shown to react with alcohols and form tertiary amines. 4-Ethyl-1,3-thiazol-2-amine can also react with carboxylic acids to form esters and with aldehydes to form acetals. This compound has been used in the synthesis of compounds such as aminothiazoles and thiazole.

2-Bromothioanisole is an enolate that is derived from the reaction of thioanisoles with a variety of solvents. This compound has been shown to have inhibitory activities against sulfoxide formation by immobilized enzymes and molecular modeling studies. 2-Bromothioanisole can be used as a substrate molecule for preparation of sulfoxide compounds using high performance liquid chromatography (HPLC). The sulfoxides formed from this compound are found to inhibit the enzyme activity in the trichloroacetic acid, trifluoroacetic acid, and sulfonic acid.

3-Bromothiophene-2-carbaldehyde is an organic compound that has been shown to have antibacterial activity. It can be synthesized by reacting triethyl orthoformate with methyl ketones in the presence of a photocatalyst such as titanium dioxide or zinc oxide. This reaction produces 3-bromothiophene-2-carboxylic acid which reacts with ammonia and hydrogen bromide to form 3-bromothiophene-2-carbaldehyde. 3-Bromothiophene-2-carbaldehyde has been shown to inhibit the growth of cancer cells and induce apoptosis, which may be due to its ability to inhibit angiogenesis. The anticancer properties are most likely due to its ability to bind DNA and inhibit protein synthesis, leading to cell death.

2-Chlorobenzyl alcohol is a chemical compound that is used to synthesize other compounds. It is produced by the reaction of ethyl formate and hydrogen chloride in a reaction vessel. It reacts with benzoates to produce 2-chlorobenzoates, which are used as intermediates in the synthesis of pharmaceuticals. Hydroxyl groups can react with hydrogen fluoride to produce hydrofluoric acid, which is used as an industrial solvent. 2-Chlorobenzyl alcohol also reacts with hydroxide ions to produce ethylene glycol, which is used in making polyester fibers and plastics. This chemical compound has structural studies that show it has a proton and two hydroxyl groups that can react with hydrogen bond. Hydrogen bonds are important for the stability of DNA structures. The molecular structures of velvetleaf plants contain 2-chlorobenzyl alcohol, which may be due to its role in transferring oxygen from leaves to roots for respiration during

2-Bromo-5-methoxybenzyl bromide is a ligand in organic chemistry. It is used as a reaction partner for the synthesis of heterocycles, such as 2-pyridone, which are biologically relevant. This ligand can be prepared by refluxing anhydrous potassium carbonate with chloroform and phenol. Macrocyclic compounds can be synthesized from this product through the Witting reaction. The efficiency of this method makes it suitable for use in biological studies.

(2S)-Pentan-2-amine hydrochloride is a versatile building block that can be used as a reaction component, reagent, or useful scaffold for the synthesis of complex organic compounds. It is a high quality chemical that can be used in both research and commercial applications. CAS No. 216237-52-4.

2-Chlorobenzyl cyanide (2CBA) is a disinfectant that has been used as an alternative to chlorine. It is not only effective against bacteria, but also against fungi, viruses, and parasites. 2CBA functions by the aerobic photooxidation of cells in water or air. In addition to its antimicrobial activity, 2CBA is also toxic to human ovary cells at high concentrations.
2CBA has a number of isomers, which differ in their solubility and ph-optimum. The most common form of 2CBA is the cis form, which has a higher solubility than the trans form. The cis form can be synthesized from benzyl chloride and sodium cyanide with sulfonation as the final step in production.
2CBA has an optimum ph value of 5-6 for its disinfectant activity; however, it can be used at a concentration of 1% at pH values below 5 or above 7

6-Chloro-1,3-dimethyluracil is a nucleoside analog that has been shown to be cytotoxic in vitro. This compound can be synthesized by reacting naphthalene with a nucleophilic nitrogen source, such as sodium carbonate and chlorinating the resulting product with trifluoroacetic acid. 6-Chloro-1,3-dimethyluracil can also be synthesized by reacting malonic acid with cyclen and uridine in the presence of copper metal. The reaction mechanism is believed to involve photoelectron transfer from the copper metal to the uridine ring.

1-(3-Bromophenyl)-2-nitropropane is a fine chemical that is used as a building block in the synthesis of complex organic compounds. It can be used as a reagent and speciality chemical with high quality. 1-(3-Bromophenyl)-2-nitropropane is versatile for use in reactions, such as coupling reactions, because it can be used as an intermediate or scaffold to create many different compounds. CAS No.: 155988-18-4

4,5-Dimethoxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate is a reagent for the synthesis of propiolates. It is prepared by reacting methyl propiolate with tetrachloride, hexachloroethane, or tetrabromide in acetonitrile. The reactants are heated to reflux under argon and then cooled to room temperature. This product is an ionic liquid that can be used as a solvent. 4,5-Dimethoxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate is a zwitterion and reacts with amines to form quaternary ammonium salts. It can also be used for the synthesis of unactivated transition metal complexes by reacting it with palladium and amines.

2,4,6-Trichlorobenzoic acid is a trifluoroacetic acid that has been used as a solvent in vitro assays and as a carbon source for kinetic studies. It has also been shown to be an effective inhibitor of bacterial growth when tested with dextrans. 2,4,6-Trichlorobenzoic acid is toxic to cells in culture and can inhibit fatty acid synthesis by inhibiting the activity of fatty acid synthase.
2,4,6-Trichlorobenzoic acid has also been found to have anti-inflammatory properties and may be useful for the treatment of asthma.