Organic Halides

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4-Bromo-2,2-diphenyl butyronitrile is an industrial chemical used in the production of other chemicals. It is a white solid that is soluble in organic solvents such as hydrochloric acid. 4-Bromo-2,2-diphenyl butyronitrile may be used to produce morphine by reacting with acetic anhydride and pyridine. This reaction occurs at a rate that is dependent on the concentration of 4-bromo-2,2-diphenyl butyronitrile. The product of this reaction has been shown to bind to opioid receptors in vitro, and it has been used as a model for pain relief in vivo. 4-Bromo-2,2-diphenyl butyronitrile also acts as a substrate for Pgp efflux pumps, which can lead to its accumulation in tissues such as the brain.

4-Amino-2-fluorobenzoic acid is a potent inhibitor of formylating enzymes, such as carbonyl reductase and amino acid formyltransferase. It has been shown to be an effective inhibitor of cancer cells in vivo and inhibits the growth of prostate cancer cells. This compound has also been shown to inhibit nitro reduction reactions, which are involved in the carcinogenic process. 4-Amino-2-fluorobenzoic acid reacts with chloride ions to produce a functional group that can react with carbon nanotubes, making it a candidate for use in cancer therapy.

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<p>DL-2,3-Diaminopropionic acid monohydrochloride is used in the preparation of drug samples for clinical chemistry analysis. This chemical has a number of uses, including as a modifier to increase the solubility and stability of drugs in solution and as a reagent to prepare analytical standards. DL-2,3-Diaminopropionic acid monohydrochloride also has been used as an inhibitor in titration methods for the determination of pH. DL-2,3-Diaminopropionic acid monohydrochloride is an inorganic chemical that can be derived from biochemical reactions by hydrolysis or derivatization. It has been shown to have selectivities for elimination reactions involving intramolecular hydrogen transfer.</p>

<p>7-Bromo-6-chloro-4(1H)-quinazolinone is a synthetic compound that is used as an intermediate in the synthesis of ethylene diamine. This substance has been shown to exhibit cytotoxicity against bladder cancer cells and tenella, as well as antiproliferative effects on human epidermal growth factor receptor (EGFR) and epidermal growth factor (EGF). 7-Bromo-6-chloro-4(1H)-quinazolinone can be synthesized in an efficient manner using butanol as a solvent. The compound has been found to exhibit cytotoxicity against tumor cells in the intestine.</p>

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<p>2-Amino-4-fluorobenzoic acid is a nitrogenous heterocyclic compound. It is an analog of the epidermal growth factor (EGF), which can bind to the EGF receptor and stimulate cell growth and differentiation. 2-Amino-4-fluorobenzoic acid has been shown to have anticancer activity in vitro, as well as in vivo. The synthetic process for this compound involves nitrous acid, hydrochloric acid, and frequency reactions. This product is used industrially for the preparation of other compounds.</p>

L-Arginine-tert-butyl ester dihydrochloride is a high quality, reagent, complex compound that is soluble in most organic solvents. It has a CAS No. of 87459-72-1 and can be used as an intermediate for the production of other chemical compounds. L-Arginine-tert-butyl ester dihydrochloride is also a useful scaffold for the synthesis of speciality chemicals or research chemicals and can be used as a versatile building block in the synthesis of many chemical compounds.

7-[4-[4-(4-Fluorobenzoyl)Piperidin-1-Yl]Butyl]-1,3-Dimethylpurine-2,6-Dione is a drug that belongs to the group of adenosine receptor antagonists. It has been shown to inhibit phosphodiesterase activity and is used as a pharmaceutical dosage. 7-[4-[4-(4-Fluorobenzoyl)Piperidin-1-Yl]Butyl]-1,3-Dimethylpurine-2,6-Dione has been shown to bind to the 5HT2C receptor in vitro. This drug may have therapeutic potential for obesity and type 2 diabetes mellitus treatment.

<p>4-(2,2-Difluoro-1,3-benzodioxol-4-yl)-1H-pyrrole-3-carbonitrile is a fungicide that inhibits the growth of fungi. It has been shown to be effective against postharvest fungal infections and synergizes with zirconium oxide. 4-(2,2-Difluoro-1,3-benzodioxol-4-yl)-1H-pyrrole-3-carbonitrile binds to copper ions and prevents ATP binding to ATP binding cassette transporter protein (ABC) transporters in fungi cells. This leads to apoptosis of these cells by inhibiting the mitochondrial electron transport chain.</p>

NMDA receptor antagonist; anti-viral; anti-Parkinsonian

<p>5-Bromo-1,3,4-thiadiazol-2-amine is a synthetic antiplatelet agent that belongs to the thiosemicarbazide class. It has been shown to have broad-spectrum antimicrobial activity against Gram-positive and Gram-negative bacteria. 5-Bromo-1,3,4-thiadiazol-2-amine is an orally bioavailable drug that can be used in the treatment of bacterial infections caused by Gram negative bacteria. The molecular modeling study suggests that this compound binds to the enzyme active site of DNA gyrase and inhibits its activity. 5Bromo-1,3,4-thiadiazol-2 amine is deuterated and can be used for molecular modeling studies because it is soluble in organic solvents.</p>

4-tert-Butyl-2,6-dimethylbenzylamine hydrochloride is a versatile building block that can be used for the synthesis of many different types of chemical compounds. It is a reagent in organic synthesis and has been used as a building block for other compounds. 4-tert-Butyl-2,6-dimethylbenzylamine hydrochloride is also useful as an intermediate or scaffold in complex syntheses. This chemical has been used in research to produce 2,4,5-trichlorotoluene and 1,2,3,5,6-pentachlorocyclohexane. CAS No. 2703627-79-4

5-Bromo-6-chloropyrazin-2-amine is a high quality, versatile building block for the synthesis of a variety of chemical compounds. It is also a reagent used in organic chemistry for the conversion of alcohols to alkyl chlorides and bromides. It can be used as an intermediate for the preparation of various complex compounds with potential use as pharmaceuticals or fine chemicals. This compound has been shown to have potential as a useful scaffold for the development of novel drugs which could be used to treat bacterial infections such as tuberculosis. 5-Bromo-6-chloropyrazin-2-amine has also been shown to be an excellent starting material for the synthesis of research chemicals and speciality chemicals.

3-(1,1,2,2-Tetrafluoroethoxy)aniline is a reagent that belongs to the group of complex compounds. It has CAS No. 831-75-4 and is used as an intermediate in the synthesis of fine chemicals, useful scaffolds and building blocks. This versatile chemical can be used as a reaction component for the production of speciality chemicals and research chemicals. 3-(1,1,2,2-Tetrafluoroethoxy)aniline can be used as a starting material for the production of other reagents such as fluoroalkylating agents and fluorinating agents.

<p>Ethyl 3,5-dichloro-4-hydroxybenzoate is a reactant in organic synthesis. It is a byproduct of the chlorination of ethyl acetate and reacts with potassium chloride to yield 3,5-dichloro-4-hydroxybenzoic acid. This reaction is catalyzed by alkali metal hydroxides or alkali metal carbonates. The esters of this acid are used as raw materials for the production of pesticides, herbicides, and pharmaceuticals. The chloride can be hydrolyzed to produce 3,5-dichloro-4-hydroxybenzoic acid.</p>

<p>Methyl 3-chloro-4-hydroxybenzoate is a wastewater treatment chemical that has been shown to be effective in the removal of chlorinated compounds such as ppcps and triclosan. It is used in pH adjustment, buffer production, corrosion control, and wastewater treatment. Methyl 3-chloro-4-hydroxybenzoate forms a complex with an alkali metal ion, which reacts with chlorine gas to form hydrochloric acid. The reaction also produces 4-hydroxybenzoic acid (4HB) as a byproduct. Treatment methods for methyl 3-chloro-4-hydroxybenzoate include chlorination and alkaline treatments.</p>

<p>2-Bromocinnamic acid is a synthetic compound that inhibits the reactions of arylating agents with tissues. It has cytotoxic activity and can be used in the treatment of alzheimer's disease. The synthesis of 2-bromocinnamic acid begins with anhydrous acetonitrile, which is heated to form an anhydrous salt. This salt is then dissolved in water and treated with potassium iodide and sodium nitrite. The resultant mixture undergoes a series of reactions to produce 2-bromocinnamic acid, including the addition of molybdenum as a catalyst. The reaction also produces byproducts that are removed by extraction or distillation. Finally, it undergoes a chromophore change from yellow to red in the presence of air due to oxidation by atmospheric oxygen.</p>

<p>3-Bromo-5-nitrobenzoic acid is a cancer drug that inhibits the proliferation of cancer cells by binding to amines, which are protonated at physiological pH. This binding leads to an electronic interaction between the bromine atom and the electron cloud of the amine group. The bromine atom is then more attracted to the nucleus, causing it to emit a photon of light. This process is called fluorescence and can be used for imaging cancer cells. 3-Bromo-5-nitrobenzoic acid also has potent antiproliferative activity against cancer cells, which may be due to its ability to bind ligands on target proteins in the cell membrane. It can also lead to apoptosis by interfering with the formation of supramolecular complexes or inhibiting protein synthesis.</p>

<p>2-(Pyridin-2-ylthio)ethyl]amine dihydrochloride is a chemical compound that has been used as a research reagent. It reacts with other compounds to produce new substances, and it can be used as a building block for more complex compounds. 2-(Pyridin-2-ylthio)ethyl]amine dihydrochloride is soluble in water and organic solvents such as acetone and ethanol, making it useful for reactions that require both types of solvents. This product also has CAS No. 40379-31-5, which means it is listed on the Chemical Abstracts Service registry. 2-(Pyridin-2-ylthio)ethyl]amine dihydrochloride has an interesting chemical structure that makes it a versatile building block or intermediate for many different reactions.</p>

<p>4,5-Dichloro-1,2,3-dithiazoliumchloride is a pyrazole ring with an acidic hydrogen. It is used as a model system to study the reactions of nucleophilic attack on amines and the low energy chemistry of pyrazoles. The compound has significant antifungal activity against Candida glabrata, which may be due to its ability to react with the carbonyl group in the active methylene. This reaction mechanism leads to inhibition of the synthesis of ergosterol and other sterols essential for fungal cell membranes.</p>

<p>Nim-trityl-L-histidine methyl ester hydrochloride is a versatile amino acid building block for the synthesis of complex compounds.</p>

<p>Gly-pro-4-methoxy-β-naphthylamide hydrochloride is a fine chemical that is useful as a versatile building block and intermediate. It is a research chemical that has been used in the production of other compounds, such as drugs, pesticides, and dyes. This compound is also used to synthesize certain polymers and plastics. Gly-pro-4-methoxy-β-naphthylamide hydrochloride has CAS number 100929-90-6, but it can be found under many other names including 4-(2′,5′dimethylphenyl)-1-(2′hydroxyethyl)piperazine (CAS 105999).</p>

<p>Sultopride hydrochloride is a drug that has been shown to be effective in treating treatment-resistant schizophrenia. It has also been shown to have cardiac effects, such as prolonging the QT interval on an electrocardiogram, and can cause amisulpride-like side effects. Sultopride hydrochloride is a dopamine receptor antagonist and it has been shown to reduce serum prolactin levels in rats. Ziprasidone, an antipsychotic drug, was found to have moderate interactions with sultopride hydrochloride. In addition, sultopride hydrochloride has been used in the past as an analytical model system for studying biological samples. This drug can also be used to treat infectious diseases, such as malaria or tuberculosis.</p>

1-(Aminomethyl)cyclopropanecarboxamide hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to be an excellent reagent for the synthesis of novel pharmaceuticals and speciality chemicals. This compound is also a useful intermediate for the preparation of high-quality products and can be used as a reaction component or scaffold in synthesis.

N-Fmoc-5-fluoro-L-tryptophan is a biologically active form of tryptophan that has been shown to have potent effects on the cardiovascular system. It is used as a tool for studying the function of angiotensin, collagen, and microstructural elements in the heart and lungs. N-Fmoc-5-fluoro-L-tryptophan has been shown to synergize with other heterocycles, maximizing its biological properties. This chemical is also effective at inducing muscle contraction in rats. N-Fmoc-5-fluoro-L-tryptophan binds to cardiothoracic proteins, causing changes in their structure that lead to increased muscle contractility. The covalent bond between this compound and the protein can be cleaved by enzymes such as proteases or nucleases, which can be useful for studying the interactions of drugs with these proteins.

5-Iodo-2-methoxybenzonitrile is a fine chemical that is used as a building block in the synthesis of other chemicals or pharmaceuticals. The compound reacts with strong bases to produce an aryl amine and iodoethane, and can be used to make derivatives as well. 5-Iodo-2-methoxybenzonitrile has a number of uses, including as a research chemical, reagent, specialty chemical, and intermediate. It is also useful in the synthesis of other complex compounds. 5-Iodo-2-methoxybenzonitrile belongs to the group of organoiodine compounds that are classified as speciality chemicals. This compound has CAS number 933672-32-3.

<p>3-Iodo-4-methylbenzamidine is a chemical building block that is used as a reagent for the synthesis of other chemicals. 3-Iodo-4-methylbenzamidine is a versatile building block that can be used to synthesize complex compounds. It can also be used to produce fine chemicals and pharmaceuticals, such as antibiotics, chemotherapeutics, and antivirals. 3-Iodo-4-methylbenzamidine has been shown in preliminary research to have anti-inflammatory properties.</p>

<p>μ-opioid receptor antagonist; management of alcohol dependence, opioid addiction</p>

<p>2,2-Dichloro-1,1,3,3-Tetrafluoropropane (DCTF) is a fluorinated ether that is used in laboratories as an anaesthetic or gas. It has been shown to be a potent inhibitor of respiration in animals and is also used to produce nitrous oxide. DCTF inhibits the enzyme cytochrome oxidase by binding to its heme group and prevents the formation of oxygen from hydrogen. DCTF is not metabolized by the body and has a half-life of about 40 minutes.</p>

2-Chlorophenylphenyl-aminomethanesulphonic acid sodium salt is a fine chemical that is a useful building block in research and development. It can be used as a reagent, a CAS No. 132141-36-7, or as a speciality chemical. This compound has been used as an intermediate in the synthesis of complex compounds. It also acts as a versatile building block for various reactions and has been used as a scaffold for the synthesis of new compounds.

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2,4-Difluoro-3-methylbenzaldehyde is a chemical compound that is used as a building block for the synthesis of other chemicals. It can be used as a research chemical or intermediate due to its versatility. 2,4-Difluoro-3-methylbenzaldehyde has a CAS number of 847502-88-9 and is classified as a speciality chemical with high quality. This compound may be useful in the synthesis of polymers and pharmaceuticals due to its ability to form covalent bonds with other molecules.

Trifluoromethoxyacetic acid is a synthetic drug that has been used to treat inflammatory bowel disease, alopecia and seborrhoea. It is also used as a pharmacological agent for the treatment of autoimmune diseases, such as sclerosis, malignant and bowel disease. Trifluoromethoxyacetic acid has anti-inflammatory properties due to its inhibition of prostaglandin synthesis. This drug has been shown to be effective in treating alopecia areata in rats with an oral dose of 0.5 mg/kg for two weeks, which is comparable to the effect observed with 1 mg/kg of minoxidil (Rogaine). Trifluoromethoxyacetic acid binds to nitrogen atoms on proteins and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division.

<p>Hexadimethrine bromide is a matrix metalloproteinase inhibitor that is used in the treatment of infectious diseases. It prevents the degradation of collagen, which is important to maintain the integrity of the extracellular matrix. Hexadimethrine bromide has been shown to be a potent inhibitor of matrix metalloproteinases and other proteases involved in collagen degradation. In addition, Hexadimethrine bromide inhibits toll-like receptor signaling, which may reduce inflammation by preventing activation of inflammatory cells such as macrophages and neutrophils. This agent also has anti-inflammatory properties that have been demonstrated in animal models.</p>

1-Chloro-1,1,2,2,3-Pentafluoropropane (HFC-245fa) is a fluorocarbon that has an electronegative and anisotropic nature. It is a liquid with a boiling point of -95°C. The chemical shift of the methyl group at 2.6 ppm in the 1H NMR spectrum is indicative of a trifluoromethyl group (-CF3). This compound is also soluble in many organic solvents. In addition to being used as a refrigerant and aerosol propellant, it is also used as a surfactant and optical brightener in plastics. Furthermore, 1-chloro-1,1,2,2,3-pentafluoropropane can react with caprylic acid to form HFC-245ea. This reaction occurs because of the steric effect of the trifluoromethyl group on the

<p>5-Chloro-1-methyl-4-nitroimidazole (5C1MI) is a fatty acid that is synthesized by the reaction of phosphorus pentachloride and an aliphatic hydrocarbon. It has been shown to be effective in treating women with breast cancer. 5C1MI blocks the activity of a protein called HER2, which promotes tumor growth. The drug has been shown to cause an increase in the number of circulating lymphocytes and natural killer cells, as well as an increase in the production of antibodies in mice. These effects are likely caused by 5C1MI's ability to inhibit the proliferation of T cells and B cells. 5C1MI has also been shown to have a high solubility in water and low solubility in lipids, which makes it suitable for administration via intravenous injection.</p>

<p>1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine is a growth factor that has been shown to bind to histone proteins and human pathogens. It has physiological effects on prostate cancer cells and fatty acid metabolism. 1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine is also antibacterial agent that has potent activity against bacterial cell walls. This drug inhibits the enzyme Clavatadine, leading to the inhibition of protein synthesis in bacteria. The spacing of nitrogen atoms in this molecule is responsible for its potent inhibition of kinase activity. 1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine is localized in the cellular cytoplasm and nucleus.</p>

7-Fluoro-1H-indole is a molecule that belongs to the class of antimicrobial agents. It has been shown to be effective against human pathogens such as P. aeruginosa and S. aureus, and has also shown hemolytic activity against erythrocytes. 7-Fluoro-1H-indole inhibits bacterial growth by binding to siderophores, which are molecules produced by bacteria in response to iron starvation, thereby blocking their uptake of iron from the environment. It has also been shown to have protease activity against Gram negative bacteria. This compound can be synthesized using an in vivo model, where it was shown that 7-fluoro-1H-indole was able to bind to the cytoplasmic membrane and inhibit protein synthesis in Gram negative bacteria cells.

4-Bromophenacyl bromide is an inhibitor of phospholipase A2. It inhibits the enzyme phospholipase A2, which is responsible for the release of arachidonic acid from membrane phospholipids. This product has been shown to inhibit the growth of cancer cells in vitro and in vivo. 4-Bromophenacyl bromide also inhibits human phospholipase A2 and is used as a research tool to study this enzyme's function.

<p>1-Phenylcyclohexanamine hydrochloride is a secondary amine that binds to the nicotinic acetylcholine receptor. It has been shown to inhibit the activity of rat liver microsomes and dopamine, with a primary amino group. The analogs of 1-phenylcyclohexanamine hydrochloride are active and have been shown to inhibit acetylcholinesterase in rat brain tissue. This inhibition leads to an increase in the neurotransmitter acetylcholine, which causes an excitatory effect on the central nervous system. 1-Phenylcyclohexanamine hydrochloride is also used as a molecular model for studying glutamate receptors because of its similar structure.</p>

<p>2-Bromo-4-(trifluoromethyl)benzyl alcohol is a versatile building block that can be used as a reactant in organic synthesis. It is also a useful intermediate and building block for complex compounds. This compound has been used as a reagent in the preparation of 2,2'-dipyridyldisulfide, which was shown to have potent antiproliferative activity against human cancer cells.</p>

<p>2-Amino-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide hydrochloride is a magnetic compound that has been shown to be an effective cancer antigen. It is a derivative of the amino acid sequence of α,β-unsaturated fatty acids and can be used as a dietary supplement. 2-Amino-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide hydrochloride has been shown to bind to fatty acid receptors on the surface of antigen presenting cells (APCs). It also activates the immune system by activating APCs, which leads to the production of cytokines and chemokines. This compound has also been shown to stimulate T cells in culture, leading to activation and proliferation of tumor cells.</p>

Ethyl 2,4-dichloroacetoacetate is a reaction component that is used as a reagent in organic synthesis. It has been shown to be a useful scaffold for the preparation of complex compounds and fine chemicals. It can also be used as a useful intermediate or building block for the synthesis of other molecules.

<p>1,1-Dibromo-2,2-difluoroethane is a chemical compound that is used as an inert gas. It has a boiling point of -37 degrees Celsius and can be seen in the infrared spectrum. The equilibrium constant for this substance is 7.4 x 10^10 and the quadratic vibrational constants are 0.0092 cm^-1.</p>

1-(2,5-Dichlorophenyl)-2-nitroethene is a chemical compound that is used as a research chemical. It's an aromatic organic compound that can be used as a versatile building block for the synthesis of complex compounds. It's also a good intermediate for many fine chemicals. 1-(2,5-Dichlorophenyl)-2-nitroethene has CAS number 1056473-63-2 and is classified as an "Aromatic Organic Chemical".

<p>5-Chloro-2-nitroaniline is a proton transport agent that is used to dissolve the stones in the kidney and bladder. It belongs to the chemical class of anilines and has a chlorine atom. This drug is structurally similar to sorafenib, which is used for cancer treatment, and has been shown to inhibit cb2 receptor activity. 5-Chloro-2-nitroaniline also reacts with hydrochloric acid or sodium hydroxide solution to produce nitrous acid, which can be used as a reactant in organic synthesis.</p>

1-Bromo-2,4-dimethoxybenzene is a functional group that can be found in nanotubes. It is synthesized by the debromination of 2,4-dibromobenzene with n-dimethylformamide and sodium bicarbonate. The reaction mechanism involves nucleophilic attack by the hydroxide ion on the bromine atom of the 1-bromo-2,4-dimethoxybenzene to form a tetrahedral intermediate followed by an elimination reaction. This process leads to the formation of carbon nanotubes. 1-Bromo-2,4-dimethoxybenzene has been shown to have anticancer activity in vitro and in vivo against breast cancer cells.

<p>α2-adrenoceptor agonist; anti-glaucoma agent</p>

<p>1-Bromo-3-isopropylbenzene is a reactive chemical that is used to produce diazotization, which is the addition of nitrite ion or its salts to an amine. This reaction produces an unstable intermediate product called diazoaminobenzene, which reacts with water and forms nitrous acid. The production of 1-bromo-3-isopropylbenzene involves the use of a deuterium isotope, which has been shown to have different effects on the reactivity of the molecule. Deuterium substitution can lead to a termination reaction rather than the desired aromatisation, as well as other reactions that are not observed when using regular hydrogen. The presence of nitrite ions in the environment can lead to deaminate reactions in 1-bromo-3-isopropylbenzene, which leads to degradation by hydrolysis and biodegradation.</p>

<p>Caesium trifluoroacetate is a polymerase chain reaction (PCR) reagent that is used to detect and quantify the presence of DNA or RNA. It can be used for the detection of DNA in water vapor, for the estimation of the number of bacteria in wastewater treatment, or to measure the amount of active drug in plasma samples. Caesium trifluoroacetate is a salt that consists of one molecule each of caesium trifluoroacetate and sodium trifluoroacetate. The ester hydrochloride form has an antiinflammatory effect, which may be due to its ability to inhibit prostaglandin synthesis.</p>

2,9-Dibromo-1,10-phenanthroline is a molecule that has been shown to be an effective sensitizer for the photochemical conversion of chlorine dioxide to ozone. It has been used as a model compound in molecular orbital calculations and has been shown to enhance the yield of ozone by up to 3%. The emission spectrum of 2,9-dibromo-1,10-phenanthroline displays a peak at 362 nm, which lies in the ultraviolet region. The molecule is orthorhombic and crystallizes in space group P2/c with cell dimensions a = 17.8 Å and c = 18.7 Å.

<p>3-Fluoro-DL-tyrosine is a model system for the study of tyrosine transfer reactions. It is used to study the reaction mechanism and kinetics of tyrosine transfer from a donor molecule to an acceptor molecule. 3-Fluoro-DL-tyrosine reacts with trifluoroacetic acid to form 3,4-dihydroxybenzoic acid, which is a chemical analog of tyrosine. The hydroxyl group on this molecule can react with the proton on the amino acid side chain, forming a covalent bond that does not break down under normal conditions. This reaction is reversible and has been shown to be catalyzed by polymerase chain reactions (PCR).</p>

3-Bromo-4-methoxybenzylamine hydrochloride is a high quality reagent that is used as an intermediate in the synthesis of complex compounds. It has been shown to be a useful scaffold for the synthesis of new chemical entities and a versatile building block for organic synthesis. 3-Bromo-4-methoxybenzylamine hydrochloride can be used as a reaction component in various chemical reactions, including Friedel-Crafts acylation, nitration, chlorination and bromination.

<p>Beta adrenergic antagonist; anti-arrhythmic</p>

N-Propyl-1-ene-2,6-diethyl-4-phenylpyridinium tetrafluoroborate (NPEEDPBF) is a fine chemical that has been used as a building block in research and industrial chemistry. The synthesis of NPEEDPBF typically involves the reaction of diethyl phenylpyridinium bromide with n propyl iodide. It can be used as a reagent for organic syntheses and as an intermediate for other compounds. NPEEDPBF is also a versatile building block for complex compounds.

9-Bromoanthracene is a benzene derivative that can be used as a chemical building block. It has a high affinity for electron-rich aromatic compounds, such as picric acid and aryl halides, which are used in the Suzuki coupling reaction. 9-Bromoanthracene also has fluorescence properties and can serve as a synchronous fluorescence probe for studies of the mechanism of this reaction. The redox potentials and constant of 9-bromoanthracene are lower than those of anthracene, which makes it more reactive towards electrophilic reactions.

2-Bromo-5-fluorocinnamic acid is a high quality, reagent, complex compound of the chemical family of phenols. It has CAS No. 939410-87-4 and is a useful intermediate in the synthesis of fine chemicals. The compound has been used as a speciality chemical for research purposes and has been found to be a versatile building block for the synthesis of new compounds. 2-Bromo-5-fluorocinnamic acid can be used as a reaction component in organic synthesis reactions, such as esterification, nucleophilic substitution, and condensation reactions.

2-Bromo-5-chlorobenzoic acid methyl ester is a chemical compound that is a component of the perborate oxidant. This chemical reacts with hydrogen peroxide to produce water, oxygen, and 2-bromo-5-chlorobenzoic acid. It can also be used in cyclisation reactions to synthesise heterocyclic compounds. The reaction mechanism for this process involves the formation of an unstable intermediate that spontaneously breaks down into two bromine atoms and one carbon atom. This process is catalyzed by metal ions such as copper, silver, and zinc. 2-Bromo-5-chlorobenzoic acid methyl ester has been used as an intermediate in the synthesis of homologues of ribonucleotide reductase.

<p>2-fluoro-5-methoxybenzaldehyde is an asymmetric synthesis that has been shown to inhibit the growth of cancer cells by inhibiting a protein called MT2. 2-Fluoro-5-methoxybenzaldehyde is a nucleophilic compound and reacts with the electrophilic carbon in the enolate to form a sulfoxide, which can be hydrolyzed by acid. This reaction inhibits cancer cell growth as it prevents cellular metabolism and amino acid biosynthesis.</p>

<p>Please enquire for more information about 3-Chloro-4-(trifluoromethoxy)aniline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-(Benzyloxy)tryptamine hydrochloride (5-BOC-TRP) is a serotonin agonist that is used to study the effects of serotonin on various tissues. 5-BOC-TRP has been shown to increase extracellular Ca2+ concentrations in receptor cells, and it has also been shown to act as an agonist at synaptic and submandibular gland levels. It binds to specific receptors in the parotid, submandibular, and other salivary glands, where it induces a release of saliva. These effects were observed when 5-BOC-TRP was administered intravenously or intraperitoneally. The distribution of this drug within the salivary glands was determined by immunoreaction with antibodies against serotonin. The localization of 5-BOC-TRP was also confirmed by whole cell patch clamp recordings obtained from rat parotid cells perfused with 5-BOC-TRP.</p>

<p>N-(5-Bromoacetamidylpentyl) acrylamide is employed in the synthesis of substrates used for nucleotide sequence determination, covalently linked to polymer coatings such as poly(N-(5-azidoacetamidylpentyl)acrylamide-co-acrylamide) (PAZAM). Polynucleotide-binding substrates find application as molecular arrays and flow cells.</p>

Selective serotonin reuptake inhibitor; anti-depressant

<p>6-Chlorochromone-2-carboxylic acid is a synthetic carboxylic acid that is a reagent in organic synthesis. It has been used to synthesize a number of new compounds, including substituted carboxylic acids and nitro compounds. The discovery of 6-chlorochromone-2-carboxylic acid was made possible by optimizing the reaction parameters, such as substituent and reaction time. This compound is cost effective and can be obtained from chromones.</p>

<p>5-Isopropylisoxazole-3-carbonyl chloride is a colorless to light yellow liquid that is soluble in organic solvents. It is used as a reagent, speciality chemical, or intermediate for the preparation of other chemicals. 5-Isopropylisoxazole-3-carbonyl chloride has been used in the synthesis of a variety of biologically active compounds, including pharmaceuticals and agrochemicals. This compound can be used as a building block for more complex molecules in both organic synthesis and biochemistry. 5-Isopropylisoxazole-3-carbonyl chloride has also been shown to have inhibitory effects on protein kinase C (PKC) and DNA topoisomerases I and II.</p>

<p>Ethyl 5-chloroindole-2-carboxylate is a pro-apoptotic agent that has been shown to inhibit the replication of HIV. It inhibits the reverse transcriptase and DNA polymerases in the virus, which prevents it from being replicated. Ethyl 5-chloroindole-2-carboxylate also induces apoptosis by alkylating the cysteine residues on the host cell's proteins. This drug is not active against other viruses, such as herpes simplex virus type 1 (HSV1). It has been shown to be an analog for cannabidiol (CBD), which binds to cannabinoid receptors CB1 and CB2.</p>

4-Bromo-2-cyanoanisole is a synthetic compound that can be used as a ligand in the transition metal catalyzed cross-coupling reaction. This chemical has been shown to form complexes with nickel, palladium, and platinum. 4-Bromo-2-cyanoanisole is also a biomolecule that interacts with other molecules and can be used in the study of natural products.

<p>Please enquire for more information about (4-(2-Fluorophenyl)piperazinyl)-N-propylformamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

2-Amino-5-chlorobenzenesulfonamide is a synthetic chemical that is used in the manufacture of amides and diazoxide. It is also found naturally in humans as a metabolite of the amino acid histidine. 2-Amino-5-chlorobenzenesulfonamide has been shown to be a potent receptor for the modulation of acetylcholine release by binding to muscarinic receptors, including M1 and M2 subtypes, and inhibiting the enzyme hydrolysis of acetylcholine. This chemical has been shown to be chemically stable at pH 5 or higher, and it has been found to be resistant to hydrolysis by enzymes such as esterases, glucuronidases, glutathione reductase, and cytochrome P450. 2-Amino-5-chlorobenzenesulfonamide is also an enantiomer that can bind to collagen in the human

N-Methylbis(trifluoroacetamide) is a molecule that is used in the preparation of an analytical method. This molecule reacts with human serum and urine to produce a reaction solution. The matrix effect can be seen in metabolic disorders, such as the case of creatine kinase which is not affected by the derivatization. N-Methylbis(trifluoroacetamide) is also used to prepare samples for solid phase microextraction with basic structures that are amines.

2-Fluoro-4-methoxyphenol is a white crystalline solid with a melting point of 100°C. It is soluble in water, ethanol and ether and insoluble in chloroform. The compound has been shown to be an intermediate for the synthesis of other organic compounds, such as 2-fluoro-4-(2,2,2-trifluoroethoxy)benzaldehyde, 2-fluoro-4-(3,3,3-trifluoropropoxy)benzaldehyde and 4-(2,2,2-trifluoroethoxy)-3'-nitroacetophenone. 2-Fluoro-4-methoxyphenol can also be used as a building block for speciality chemicals including research chemicals.

3-Chlorobenzaldehyde is a chemical that is used as a diagnostic agent for mitochondrial diseases. 3-Chlorobenzaldehyde can be used to detect mutations in the mtDNA and diagnose deficiencies of enzymes involved in energy metabolism. It has been shown to inhibit the activity of dehydrogenase enzymes and the synthesis of acyl-coa from zirconium oxide, which is an important component in polymerase chain reactions. This chemical also inhibits mitochondrial functions and enzyme activities, making it useful for screening for drugs that affect these processes. 3-Chlorobenzaldehyde has also been shown to inhibit hydrogen fluoride, which is often found in industrial environments.

<p>N-Bromophthalimide is a hydrogen bond acceptor that is used in pharmaceutical preparations. It has been shown to be an effective cationic surfactant, which may be due to its ability to form ionic bonds with phosphotungstic acid and nitrogen atoms. N-Bromophthalimide also has reactive properties and can react with serotonin reuptake inhibitors. The reaction mechanism of this compound is not fully understood, but it has been shown to have a redox potential that is greater than the standard electron donor sodium bromide.</p>

<p>6-Chloro-7-methylchromone-2-carboxylic acid is a fine chemical that has been used as a versatile building block for the synthesis of complex compounds. It has been shown to be an effective reaction component in the synthesis of 1,4-benzoquinones and N'-acylhydrazones. 6-Chloro-7-methylchromone-2-carboxylic acid is also a useful intermediate in the preparation of other chemicals, such as pharmaceuticals and pesticides. This compound can be used as an additive to improve the quality of high purity reagents.</p>

Please enquire for more information about N-(4-(4-bromophenyl)-2,5-thiazolyl)hexanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>3-Bromo-4-fluorocinnamic acid is a useful intermediate that reacts with amines to form 3-bromo-4-fluoroaniline, which is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.</p>

<p>9-Fluorenone oxime is a pharmacological agent that has been shown to inhibit the activity of proteases. It has been shown to be effective in the treatment of hepatitis caused by radiation and amines, such as fluorenone. 9-Fluorenone oxime binds to the hydroxyl group of the active site on the protease enzyme and forms a covalent bond with it. This prevents hydrolysis of substrate proteins and thus blocks protein synthesis. 9-Fluorenone oxime also has chelate ligand properties, which allow it to bind to metal ions, such as phosphotungstic acid or fluorescence probes, and form complexes. The thermal expansion property of 9-fluorenones can be used for thermometry in biochemistry research.</p>

<p>4-Chloro-2-methylbenzyl alcohol is an organic compound that has a sensor and hydroxyl group. It is used in pest control as an insecticide. 4-Chloro-2-methylbenzyl alcohol has been shown to be effective against ants, cockroaches, and other insects. There are multiple instabilities of this compound, including low oxygen stability when exposed to air, which may lead to the degradation of this chemical. Impurities in 4-chloro-2-methylbenzyl alcohol may also lead to its instability as it reacts with alkali metals at high temperatures. The instability of 4-chloro-2-methylbenzyl alcohol can be reduced by storing it at low temperatures or by adding cryogenic substances such as liquid nitrogen or carbon dioxide gas.</p>

<p>3-Bromo-4-hydroxybenzaldehyde is a fluorescence probe that can be used to identify the presence of hydroxyl groups in organic solutions. It reacts with hydrochloric acid to form a green solution and a gas. 3-Bromo-4-hydroxybenzaldehyde has been used to study hydroxyl groups in human serum, plant physiology, and surfactant sodium dodecyl (SDS). This compound has shown potent inhibition against an enzyme called benzoyl peroxide reductase. 3-Bromo-4-hydroxybenzaldehyde is soluble in water, but not in ether. The molecular weight of this compound is 176.3 g/mol.</p>

<p>Methyl 3-amino-5,6-dichloro-2-pyrazine carboxylate is a synthetic molecule that has been synthesized from dimethylamiloride. This chemical has been labeled and used for a variety of homologous and synthetic modifications. It may be used in labeling experiments to identify an unknown compound or to determine the structure of a known compound. The methyl 3-amino-5,6-dichloro-2-pyrazine carboxylate can also be used as a ligand to bind with subunits of proteins or nucleic acids. Photolabile methyl 3-amino-5,6-dichloro-2-pyrazine carboxylate can be synthesized by using light energy to cleave the ester bonds in the chemical. This chemical is useful for assays and techniques such as spectroscopy and nuclear magnetic resonance (NMR).</p>

<p>N-[2-(2,3-Dimethoxyphenyl)ethyl]-2-chlorobenzamide is a versatile building block that can be used as a reaction component and reagent. It is an intermediate in the synthesis of pharmaceuticals and fine chemicals and has been shown to be useful in the synthesis of complex compounds. This compound reacts with nucleophiles, such as amines and alcohols, by replacing the chloride group with a variety of functional groups. The product is then hydrolyzed to release the original reactant. N-[2-(2,3-Dimethoxyphenyl)ethyl]-2-chlorobenzamide has a CAS number of 320576-19-0 and can be found at ChemDiv.com.</p>

4-Bromoresorcinol is a synthetic compound that belongs to the group of sulfonamides. It is used in the production of dyes, pharmaceuticals, and agricultural chemicals. 4-Bromoresorcinol is synthesized by sulfonation with trifluoroacetic acid followed by hydrolysis with hydrochloric acid. The polymerization kinetics of this compound have been studied using azobenzene as a model substrate. The reaction products are vignafuran and an organic solvent (e.g., methanol). In addition, 4-bromoresorcinol has potent antibacterial activity against bacteria such as Staphylococcus aureus and Mycobacterium tuberculosis. This drug has minimal inhibitory concentrations (MICs) less than 0.01 ppm for most strains of bacteria tested, including those resistant to penicillin G or erythromycin. The drug also inhibits hydroxylase enzymes

<p>2-Aminoethoxyamine dihydrochloride is a cardiotonic, which is a chemical agent that acts on the heart to increase contractility. It has been shown to be more efficient and less toxic than other cardiotonics. 2-Aminoethoxyamine dihydrochloride has been found to act as an epoxidizing agent and can be used in the synthesis of istaroxime, an inhibitor of cholesterol biosynthesis.2-Aminoethoxyamine dihydrochloride also reacts with dehydroepiandrosterone to form 2-aminoethoxyamidine hydrochloride.</p>