Organic Halides

1,1,2-Trichloro-1-fluoropropane is a solvent used in the production of fluorinated organic compounds. It is used as an intermediate for the manufacture of refrigerants and aerosol propellants. 1,1,2-Trichloro-1-fluoropropane has been shown to have a significant impact on the environment due to its high volatility and solubility. The emission of this chemical into the atmosphere can deplete ozone levels and cause damage to vegetation. This chemical also has a high vapor pressure and can be fatal if inhaled or absorbed through the skin. In addition, 1,1,2-Trichloro-1-fluoropropane is toxic to aquatic life because it is soluble in water and accumulates in fatty tissues of living organisms.

6-Chloro-7-methyl-3-formylchromone is a magnetic nanoparticle that can be used in the detection of coordination compounds. The coordination compound is first reduced to form the corresponding phosphoryl complex, which is then detected by the change in color and intensity of the magnetic nanoparticles. This reaction is linear over a wide range of concentrations and pH values and does not require additional reagents or solvents. The colorimetric method for this reaction has been shown to be effective for detecting ursolic acid, zirconium, gold nanoparticles, and linear ranges.br>br>
The phosphatase PTP1B enzyme is responsible for regulating glucose levels in cells. It has been shown that 6-chloro-7-methyl-3-formylchromone inhibits PTP1B activity by dephosphorylation at cysteine residues. This inhibition leads to increased glucose uptake and decreased insulin release from pancreatic beta cells

H-Gly-Arg-AMC hydrochloride salt is a substrate for the enzymes cathepsins B, H, and L. This compound has been used to measure protease activity in cell culture and as a diagnostic substrate for peptidases. The enzyme reaction can be monitored by measuring changes in the fluorescence of the product at 340 nm. The pH optimum for this enzyme is 7.4.

6-Bromo-4-fluoro-2-methyl-1-propan-2-ylbenzimidazole is an environmental pollutant that can be found in deionized water, as a result of the reaction between hydrochloric acid and benzene. It has been synthesized using the industrial synthesis method by reacting n-hexane with sodium sulfate, followed by treatment with acetone and hydriodic acid. 6BFMBI is a white solid that reacts with hydrogen to produce acetone and formaldehyde. The reaction time for this compound is about three hours at room temperature.

Please enquire for more information about Nd-Z-L-ornithine methyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

(1S,4S)-1,7,7-Trimethyl-3-(Trifluoroacetyl)Bicyclo[2.2.1]Heptan-2-One is a white solid with a melting point of -76.8°C and a boiling point of 265°C at 10 mm Hg. It has the following functional groups: particle, luminescent, lanthanide, stabilizer, ligand, voltammetry, thermally stable and has nmr spectra that show light emission and coordination chemistry. This compound is a sulfoxide but can also be considered to be a phosphine or an amine depending on its structural features. The compound's nature is dependent on the temperature and pressure as well as the solvent it is being dissolved in.>>END>>

5-Amino-2-chlorobenzonitrile is a functional theory that has been optimised for the synthesis of pesticides. It has been shown to have high affinity constants and to be a good potential for monitoring. 5-Amino-2-chlorobenzonitrile is synthesized in the form of monoclonal antibodies, which are then optimised using vibrational frequencies. The parameters of these molecules are optimized by comparing the calculated frequencies with those obtained from experimental data. This theory can be used to develop new pesticides that are less harmful to humans and animals, as well as being more environmentally friendly.

3-Chloro-4-methylbenzyl alcohol is a building block chemical that is used in the synthesis of a variety of organic compounds. It is a versatile chemical that can be used as a reagent, reaction component, and intermediate. 3-Chloro-4-methylbenzyl alcohol has been found to be useful in the synthesis of complex compounds, such as 4-chloromethoxybenzoic acid and 3-(3,5-dimethoxyphenyl)acetic acid. This chemical can also be used to produce speciality chemicals, such as 3-(2-(2,4-dichlorophenoxy)ethyl)benzonitrile.

1,5-Dichloroanthraquinone is a chlorine atom with a carbonyl group that is a reactive synthetic intermediate. It is used in the synthesis of palladium complexes. 1,5-Dichloroanthraquinone has been shown to react with hydrochloric acid to form an anhydrous sodium salt and calcium carbonate. The fluorescence properties of this compound have also been studied. 1,5-Dichloroanthraquinone has been found to be cytotoxic in vitro and the reaction mechanism has been determined by vibrational spectroscopy and x-ray crystal structures.

Trichlorosan is a biocide that is used as a disinfectant and preservative, and has also been shown to have antibacterial properties. It is often used in industrial settings to inhibit the growth of bacteria in process water, cooling towers, and wastewater treatment systems. Trichlorosan has been shown to be genotoxic in rats at high doses. This chemical can be found in personal care products such as soaps, toothpaste, mouthwash, deodorants, or body lotion. It can also be found in some household items such as kitchenware, clothes and bedding. Triclosan is one of the active ingredients in trichlorosan that prevents bacterial growth by binding to the enzyme that catalyzes the conversion of glycerol to fatty acids and lysing cells through cell membrane disruption. The enzyme activity index for triclosan was determined by measuring the amount of time it takes for a solution containing benzalkonium chloride (B

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.

Please enquire for more information about N-α-Boc-L-ornithine tert-butyl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Amino-2-fluorobenzoic acid (5AFBA) is a synthetic aniline that is used as a fluoroquinolone antibiotic. 5AFBA inhibits the synthesis of trehalose, which is vital for bacterial growth. This drug also has been shown to be active against Mycobacterium tuberculosis and Mycobacterium avium complex. 5AFBA has also been shown to have antifungal properties, inhibiting the synthesis of ergosterol in the fungal cell membrane. 5AFBA can be modified by alkylation with geranyl groups or N-methylation at the amino group. These modifications have been shown to increase its antibacterial activity against Pseudomonas aeruginosa.

5-Iodo-2,3-dimethoxybenzoic acid (5IMB) is a synthetic chemical that is used as a radiolabeled substrate for the synthesis of dopamine. The 5IMB is a substrate for the enzyme monoamine oxidase, which converts it to 5-hydroxyindoleacetic acid (5HIAA). The intensity of the signal emitted by 5IMB increases with the increase in concentration of dopamine. It can be used as a positron emission tomography (PET) tracer for dopamine receptors in the brain. The kinetic and uptake properties of 5IMB are different in various regions of the brain, such as striatum and caudate putamen. This difference can be measured using high-performance liquid chromatography (HPLC) and flow rate.
5IMB has been shown to have anti-oxidant properties due to its ability to scavenge peroxide radicals.

4-Bromo-3-nitrotoluene is a carbazole that has been found to have insecticidal activity. The compound reacts with serotonin to form the reactive intermediate 4-bromo-3-nitrosobenzaldehyde, which is then oxidized to the final product 4-bromo-3-nitrobenzoic acid. The insecticidal activity of 4-Bromo-3-nitrotoluene was found to be due in part to its ability to inhibit serotonin uptake and metabolism by blocking serotonin transporters. It also induces dihedral angles in positron emission tomography (PET) imaging of human brain tissue, suggesting it may be useful for brain imaging studies.

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.

6,6'-Dibromoindigo is a substrate for enzymes that catalyze the oxidation of aromatic compounds. It can be used to measure the activity of these enzymes in biological samples. 6,6'-Dibromoindigo is also an inhibitor of human pathogens, such as Escherichia coli and Proteus mirabilis. It has been shown to have an apoptotic effect on certain cells in a model system and to inhibit HIV-1 protease. 6,6'-Dibromoindigo binds to the receptors of some bacteria and inhibits their growth by binding to cysteine residues within the bacterial cell wall. This binding prevents formation of the final product from 2 molecules of pyruvic acid, which inhibits oxidative phosphorylation and energy production by mitochondria.

2-Chloro-1,3-dimethyl-1H-benzimidazol-3-ium chloride is a chemoenzymatic that has a role in the process of ovary development. It is an endogenous substance that can be analysed by lectin immunoassay and antibody binding. 2-Chloro-1,3-dimethyl-1H-benzimidazol-3-ium chloride is a ligand for the lectin domain of the cell membrane and it can be used as a strategy for transfection. This chemical binds to receptors on the cell membrane and stimulates signalling pathways within cells. The biochemical activity of 2CMDMBICL can be analyzed using biochemical techniques such as immunoprecipitation or enzyme assays.

4-Chloro-2-methylaniline (CMA) is a chemical that belongs to the group of amines and is used as an intermediate in the manufacture of dyes, pesticides and pharmaceuticals. CMA has been shown to be toxic to humans through skin contact, inhalation or ingestion. This substance also disrupts the activity of enzymes such as acetylcholinesterase, which is responsible for breaking down acetylcholine and regulating muscle contractions. Long-term exposure to this chemical may lead to bladder cancer. CMA can also be used as a model for carcinogenic potential studies due to its ability to induce cancer in animals.

Please enquire for more information about 2-(4-Chlorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Pyridine selenyl bromide is a co-precursor for the synthesis of 2-selenides. It can be prepared by reacting 2-pyridinesulfonyl chloride with sodium periodate in acetonitrile. This compound can then be converted to a 2-selenide by treatment with methanol and periodic acid. The analytical and preparative methods are shown below:
Analytical: Dissolve the sample in dichloromethane, add triethylamine, and extract into diethyl ether. Add a small amount of potassium bromide to the organic layer and evaporate to dryness under vacuum. Recrystallize from acetonitrile.
Methanolysis: Dissolve the sample in methanol, add a catalytic amount of hydrochloric acid, and heat at reflux for 12 hours. Cool the solution, filter off any insoluble material, evaporate to dryness

2,3,4,5,6-Pentafluoro-L-phenylalanine (PFPA) is a substrate molecule that has been shown to inhibit the α1 subunit of the Na+/K+ ATPase in human heart cells. PFPA also inhibits the growth of bacteria in culture and is active against bacterial strains that have developed resistance to other antimicrobial agents. PFPA is also effective against bowel disease caused by H. pylori. PFPA has been shown to inhibit the production of an antimicrobial peptide by hl-60 cells in vitro and has been shown to be effective against a number of infectious diseases including tuberculosis and some autoimmune diseases.

Trifluoroacetaldehyde is a chemical with aqueous solubility of 0.2 g/L at 25 °C. It has been used in the preparation of insoluble polymers, such as phosphonates and polyurethanes. Trifluoroacetaldehyde can be prepared by reacting anhydrous hydrogen fluoride with trifluoroacetic acid in the presence of amines and an oxidizing agent, such as phosphorus pentoxide. The reaction mechanism is believed to involve a cationic polymerization involving hydrolysis of the amine to give an ammonium ion that reacts with hydrogen fluoride to form trifluoroacetyl fluoride and ammonium chloride. Trifluoroacetaldehyde has also been used in asymmetric synthesis, hydroxyl group reactions, pharmaceutical preparations, and monoclonal antibody production.

Please enquire for more information about N-(2-(3,4-dimethoxyphenyl)ethyl)(4-chlorophenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-Amino-1-(1-aza-2-(2,4-dichlorophenyl)vinyl)ethene-1,2-dicarbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

(Fluoro-Methylphosphoryl)Oxycyclohexane is an organophosphorus compound that acts as a nerve agent. It inhibits the enzyme acetylcholinesterase, which is responsible for breaking down acetylcholine, leading to excess cholinergic stimulation. This can cause excessive contraction of muscles or even death. The exposure to (Fluoro-Methylphosphoryl)Oxycyclohexane can be detected by analytical methods such as gas chromatography/mass spectrometry. Oximes are used in the reactivation of acetylcholinesterase and are effective in preventing neuronal death. They bind to the phosphonyl group in (Fluoro-Methylphosphoryl)Oxycyclohexane and prevent it from inhibiting the enzyme acetylcholinesterase.

2,5-Dichloropyrimidine is a cytotoxic drug that is activated by acetonitrile to form an intermediate, which is then converted to the active form. This drug has been shown to be neuroprotective in animal models of neurodegenerative diseases. 2,5-Dichloropyrimidine also blocks the production of nitric oxide by binding to the factor receptor and prevents activation of the growth factor. The drug has been shown to inhibit the growth of cancer cells in vitro and in vivo.

Perfluoroalkylethyl acrylate is a chemical compound that belongs to the group of fluorinated aliphatic hydrocarbons. It is stable in low light and is resistant to oxidation. The polymerization of perfluoroalkylethyl acrylate can be achieved by heating with phosphorus pentachloride, sodium carbonate, and a cationic surfactant under constant pressure at an optimal reaction temperature. Perfluoroalkylethyl acrylate has been used as a monomer for the synthesis of polyfluoroalkyl methacrylates, which have been shown to have high durability and chemical stability.

(4-Iodophenyl)hydrazine hydroiodide is a synthetic compound that has shown anti-viral activity against HIV and cytomegalovirus. It also has anticancer properties and can be used to treat colon cancer. The compound binds to the nucleic acid in a number of ways, including by forming reversible covalent bonds with functional groups on the nucleic acid. These interactions are primarily due to its pyrazole ring and hydrazine moiety. (4-Iodophenyl)hydrazine hydroiodide is structurally similar to phenyldiazenyl, which exhibits photochromism and fluorescence properties. This similarity may account for the observed photochemical changes in the molecule when exposed to light.

Tetraheptylammonium bromide is a solid catalyst that can be used for the preparation of pyrimidine compounds. Tetraheptylammonium bromide is a phase transition material with a melting point of about -60°C. It is used as an analytical reagent in the determination of metal ions by solution equilibria, and has been shown to have hemolytic activity. Tetraheptylammonium bromide has been shown to be a selective hydroxyl group-containing compound, which can be used in analytical chemistry methods such as linear calibration curves and carbon disulfide titrations.

Muscarinic antagonist; bronchodilator

2-Iminothiolane hydrochloride is an amine that reacts with free thiol groups in proteins. It can be used to generate models of protein structures, as well as to study the effects of disulfide bonds on protein stability and function. 2-Iminothiolane hydrochloride has been shown to inhibit HIV infection by blocking the uptake of all-trans retinoic acid into cells. This drug also has minimal toxicity and can be used for cancer therapy. The drug was shown to have minimal toxicity in vitro, but it has not yet been tested in vivo.

Bis(2,2,2-trichloroethyl)azodicarboxylate is a nucleophile that can be used as an alkylating agent in the industrial process. It is also used to prepare chiral amines by adding an amine to the enantiomerically pure bis(2,2,2-trichloroethyl)azodicarboxylate. The anticancer activity of Bis(2,2,2-trichloroethyl)azodicarboxylate is due to its ability to inhibit tumor cell proliferation. Bis(2,2,2-trichloroethyl)azodicarboxylate is not effective against cancerous cells that do not have functional groups such as amino acids.

μ-opioid receptor antagonist; management of alcohol dependence, opioid addiction

PDE5 enzyme inhibitor

Methyl 2,4-dibromobenzoate is used as a coupling agent in organic chemistry. It is a reactive intermediate that can be used to carry out oxidative cyclizations. This compound is also an efficient catalyst for the amination of ketones and aryl bromides with palladium catalysis. Methyl 2,4-dibromobenzoate may also be used to achieve the oxidative cyclization of electron-deficient alkenes with palladium catalysts.

p-Azidophenacyl bromide is an enzyme form that catalyzes the hydrolysis of azides, such as nitrobenzene. It is chemically stable and can be used in human serum. The enzyme form has been shown to hydrolyze DNA with high specificity and low background. p-Azidophenacyl bromide also has antiviral properties against herpes simplex virus because it inhibits the synthesis of viral DNA. This enzyme form also binds to benzyl groups on the surface of cell membranes, which are part of a ternary complex formation with lysine residues and hydroxyl groups. p-Azidophenacyl bromide is present in mitochondria and cytochrome plasma mass spectrometry has shown that it is a mitochondrial cytochrome.

4-Amino-5-chloro-2-ethoxybenzoic acid is a phenoxy compound that is synthesized in the laboratory. The chemical structure of this compound has been studied using high performance liquid chromatography and it was found to have pharmacokinetic properties that are consistent with those of other drugs in its class. This drug is being developed as an anti-depressant, targeting the 5HT4 receptor. The bioactive metabolite of 4-amino-5-chloro-2-ethoxybenzoic acid is 4-(4′ hydroxybutyl)phenol, which has been shown to be a potent inhibitor of phosphodiesterase activity.

Produces fluorescent benzimidazole derivatives; detects aromatic aldehydes

1,1,2,2,3,3,4,4,5,5-Decafluorocyclopentane is a fluorocarbon liquid with a boiling point of -50°C. It has an average particle diameter of 0.1 nm and a water vapor pressure of 1.6 × 10-10 torr at 20°C. Due to its non-polarity and low viscosity (1 cP), it can be used as a solvent in organic chemistry reactions. 1,1,2,2,3,3,4,4,5,5-Decafluorocyclopentane has been shown to be reactive at the target site due to its acid molecules that provide the reactive sites for this molecule's phase transition temperature (-52°C) and nmr spectra. The reactive sites also allow for x-ray structures to be obtained by imaging techniques such as electron microscopy or atomic force microscopy.

5-(Trifluoromethyl)benzene-1,3-diamine is a chemical compound that is used in the synthesis of coatings and magnetic resonance imaging contrast agents. It can be used as a crosslinker for polymers, such as amides, in order to improve their hardness and strength. The synthesis of 5-(trifluoromethyl)benzene-1,3-diamine is done by reacting hydrogen chloride with magnesium oxide in an organic solvent. The product can then be reacted with other compounds to produce different products. One such compound is benzotrifluoride, which can be used to synthesize fluorinated coatings and monomers. The final product can also be reacted with sodium formate to produce a constant.

3-Amino-4-fluorobenzoic acid ethyl ester is a linker that is used to attach a drug molecule to the tautomycin, an analgesic. It has been shown to have nontoxic properties in animals and does not react with intestinal contents. The 3-Amino-4-fluorobenzoic acid ethyl ester also reacts with azide, phosphatase, and hydrocarbons. It is stable in the presence of aromatic hydrocarbons and can be used as a photolabeling agent for introducing a fluorescent group into a molecule.

1,1,2-Tribromo-1,2-Difluoroethane is a gaseous chemical that is soluble in salt solution. It can be solubilized in organic solvents such as ethers, chloroform, and carbon tetrachloride. The compound hydrolyzes at high temperatures and thermally decomposes at temperatures above 100°C. It also reacts with water to release hydrogen bromide and hydrogen fluoride gas. This chemical has been shown to inhibit the growth of many bacteria by inhibiting protein synthesis. 1,1,2-Tribromo-1,2-Difluoroethane is used as an industrial solvent and can be injected into the body or introduced into the body by other methods such as inhalation or ingestion. 1,1,2-Tribromo-1,2-Difluoroethane is hydrophobic and has a molecular weight of about 186 grams

1-(4-Chlorophenyl)-2-nitropropene is a versatile building block that can be used in the synthesis of a variety of compounds. It is an aromatic compound with a molecular weight of 122.1 and chemical formula CHClNO. It has a melting point of -44°C, boiling point of 166°C, and density at 20°C of 1.11 g/mL. This product has also been shown to be useful as an intermediate or reaction component for the synthesis of polymers, pharmaceuticals, pesticides, and other organic compounds. 1-(4-Chlorophenyl)-2-nitropropene is soluble in water (10 mg/mL) and alcohols (10 mg/mL). This product is classified as not hazardous according to the Globally Harmonized System (GHS) criteria for classification and labeling of chemicals.

5-Amino-4,6-dichloropyrimidine is a fluorescent probe that can be used in the detection of nucleophiles. It has been shown to inhibit the growth of cells infected with herpes simplex virus and hl-60 cells. This compound has also been shown to have nicotinic acetylcholine receptor activity and can be used as an analog for purines. The nitrogen atoms in this molecule are responsible for its anti-cancer properties. 5-Amino-4,6-dichloropyrimidine binds to epidermal growth factor (EGF) and blocks its binding site on the cell surface, reducing cancer cell proliferation. Benzyl groups on either end of this molecule act as a protective group against acid hydrolysis, making it stable in acidic environments such as stomach acid. This drug also contains chlorine atoms that make it easy to synthesize and purify by reacting with trifluoroacetic acid.

Isothipendyl hydrochloride is a crystalline cellulose derivative that is used as an excipient in pharmaceutical preparations. It has been shown to inhibit the growth of animal cells and bacteria, including Gram-positive and Gram-negative bacteria, with optimum concentrations ranging from 3 to 30%. Isothipendyl hydrochloride has also been shown to have anti-inflammatory properties against inflammatory diseases, such as allergic rhinitis and asthma. Isothipendyl hydrochloride may also be used for the treatment of autoimmune diseases, such as psoriasis or rheumatoid arthritis. Isothipendyl hydrochloride has also been shown to have anti-cancer activity, inhibiting skin cancer cell growth. This may be due to its effects on receptor activity by inhibiting certain cellular functions necessary for tumor cell proliferation. Isothipendyl hydrochloride can be prepared by reacting thiourea with 2-aminoethanol followed by hydro

2-[4-(2,2-Dichlorocyclopropyl)phenoxy]-2-methylpropanoic acid (CGP) is a drug that blocks the nuclear receptor PPARγ. It has been shown to reduce cholesterol levels by inhibiting the synthesis of cholesterol, as well as reducing liver lesions in vivo. CGP also inhibits the growth of cancer cells through its ability to bind to DNA and regulate transcriptional activity. The response element for this compound is found in the promoter region of the gene encoding the growth factor-β1 (GF-β1), which is an important regulator of cell proliferation, differentiation, and apoptosis. CGP also inhibits peroxisome proliferator activator receptor α (PPARα) and γ (PPARγ). This inhibition leads to decreased expression of genes involved in lipid metabolism, such as acyl CoA synthase and fatty acid synthetase. CGP has also been shown to be carcinogenic in vivo

2-Chloro-5-hydroxybenzoic acid is a compound that contains a hydroxyl group. It is an organic acid and a monomer that can be used in the preparation of coumarin derivatives. 2-Chloro-5-hydroxybenzoic acid can be prepared by oxidation of 2,3,4,5,6 tetrahydrobenzoquinone with hydrogen peroxide followed by hydrolysis. The oxidation step is carried out using potassium permanganate as oxidant and activated manganese dioxide as catalyst. This method yields the desired product in high yield.

1,4-Dibromo-2,3-butandiol is a halogenated butandiol.

Please enquire for more information about 4-Chloro-3',4'-dimethoxychalcone including the price, delivery time and more detailed product information at the technical inquiry form on this page