Organic Halides

Please enquire for more information about 3-Bromo-6-methylpicolinic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Bromo-2-nitro-1H-imidazole (4BNI) is a synthetic drug that is used in the treatment of cancer. 4BNI inhibits the synthesis of DNA, which leads to cell death by preventing the production of proteins vital for cell division. When 4BNI is taken up by cells it becomes activated and binds to DNA, inhibiting the synthesis of RNA and protein. This process eventually leads to apoptosis (cell death). 4BNI has been shown to be effective against tumors in mice, but has not yet been tested on humans. The uptake of 4BNI in tumor tissue can be visualized using hypoxia imaging techniques such as positron emission tomography or magnetic resonance imaging.

1-Bromo-3,3-dimethylbutane is an alkali metal compound that can be used as a substitute for ethylene. It is expressed in the liquid phase and reacts with halogens to form reactive intermediates. These reactive intermediates react with other molecules to cause bond cleavage. The reaction time is dependent on the temperature of the system. 1-Bromo-3,3-dimethylbutane has three isomers that are formed during the reaction: 2-, 3-, and 4-bromohexane. The mechanism for this reaction involves a single electron transfer from one molecule to another, which causes a series of reactions that leads to the formation of 1-bromo-3,3-dimethylbutane. This process occurs spontaneously due to irradiation by ultraviolet light or electron beams.

(±)-DoiHydrochloride is a serotonergic drug that belongs to the group of serotonin reuptake inhibitors. It affects the serotonergic system by inhibiting serotonin reuptake, which leads to increased synaptic concentrations of serotonin. This in turn activates signal pathways and increases levels of dopamine, norepinephrine, and epinephrine. (±)-DoiHydrochloride has antioxidative properties and can be used for the treatment of chronic schizophrenia. It was shown to be effective in patients with atrial fibrillation who were not responding well to other treatments.

Trifluoroacetate salt

3,5-Diiodothyroformic acid is a fine chemical that is used as a versatile building block in organic synthesis. It is also an intermediate for research chemicals and speciality chemicals. In addition to its use as a reagent, 3,5-Diiodothyroformic acid has been shown to be useful as a building block for the synthesis of pharmaceuticals and agricultural chemicals.

Please enquire for more information about pTH (28-48) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Fluoro-2-nitrobenzaldehyde is a pyridine derivative that has been used in the synthesis of a number of important heterocyclic compounds. This compound can be prepared by reacting 3,4-dichloroaniline with nitrous acid and then hydrolyzing the resulting 3-chloroquinoline with hydrochloric acid. The reaction yields anilines and quinolines in regiospecifically, as well as formylation, cyclisation, and condensation products. It is also capable of aromatisation reactions with benzene to produce benzofuran derivatives.

Please enquire for more information about Fluorescein-6-carbonyl-Ala-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Biotinyl-Obestatin (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Desmethyl sibutramine hydrochloride salt is a pharmaceutical preparation that has been used in the treatment of depression and chronic pain. It is a synthetic drug that increases the level of dopamine in the brain by inhibiting its reuptake. In addition, it has been shown to be effective in the treatment of hyperactivity, diabetic neuropathy, and other amines. Desmethyl sibutramine hydrochloride salt also has an antidepressant effect by decreasing serotonin reuptake.

Please enquire for more information about PAR-2 (1-6) (mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Iodo-1-methyl-1H-imidazole is a trifluoroethylamine that inhibits the activity of tyrosine kinases. It binds to the active site of tyrosine kinase and prevents the binding of ATP, preventing phosphorylation and activation of downstream substrates. 4-Iodo-1-methyl-1H-imidazole has been shown to inhibit the proliferation of tumor xenografts in mice, as well as inhibiting headgroup binding and cellular proliferation in vitro. This agent also has a nanomolar range and high selectivity for protein kinases, which may make it suitable for therapeutic purposes.

Please enquire for more information about Fluorescein-6-carbonyl-Ile-Glu(OMe)-Thr-DL-Asp(OMe)-fluoromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (Phe2, Nle 4)-ACTH (1-24) (human, bovine, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Abz-Lys-Pro-Leu-Gly-Leu-Dap (Dnp)-Ala-Arg-NH2 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Fluorescein-6-carbonyl-Leu-Glu(OMe)-His-DL-Asp(OMe)-fluoromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-Bromoindazole is a hydrogen bond inhibitor that has potential neuroprotective effects. It inhibits the enzyme DNA Gyrase, which is necessary for bacterial replication, and has antibacterial properties. 6-Bromoindazole interacts with the receptor tyrosine kinase axitinib and inhibits its activity. This interaction may be responsible for its neuroprotective effects.

Intermediate in the synthesis of dapagliflozin

3-Fluoroamphetamine hydrochloride (3FAH) is a histological and microscopic technique used to study the effects of analgesics on human skin. 3FAH is an analgesic that has been shown to reduce pain in a number of studies. It has also been observed to enhance the effects of laser treatments on human skin, as it reduces inflammation and increases transdermal permeation. This drug is applied topically or injected for the treatment of pain, muscle spasms, or Parkinson’s disease. 3FAH can be administered by iontophoresis or permeation techniques, which are both effective ways to deliver drugs through skin.

2-Chlorophenyl)diphenylmethanol is an antifungal drug that blocks the function of a calcium ionophore in fungal cells. It has been shown to be effective against a variety of filamentous fungi, including Aspergillus fumigatus, Candida albicans, and Trichosporon cutaneum. This drug is used as a topical antifungal agent for treatment of skin infections caused by these fungi. 2-Chlorophenyl)diphenylmethanol has been shown to have anti-inflammatory properties in animal models of kidney fibrosis and cell binding. Clinical data suggests that it can be used for the prevention or treatment of stem cell transplantation complications such as graft versus host disease and leukemia.

Please enquire for more information about (2E)-1-[5,6-Dihydro-3-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyrazin-7(8H)-yl]-4-(2,4,5-trifluorophenyl)-2-buten-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Amino-6-fluorobenzoic acid ethyl ester is a chemical that can be used as a building block in the synthesis of more complex compounds. It is a versatile intermediate and can be used to synthesize other important compounds, such as pharmaceuticals. This compound has been shown to be useful for the preparation of 2-amino-4,6-difluorobenzoic acid ethyl ester and many other derivatives. The colorless solid is soluble in ether and dichloromethane.

4-Chloro-3-fluorobenzaldehyde is an atypical molecule that has a deuterium atom. It is classified as a group p2 functional theory reuptake inhibitor, which blocks the reuptake of noradrenaline at the synapse. The vibrational and spectroscopic properties of this molecule are similar to those of other molecules in its class. 4-Chloro-3-fluorobenzaldehyde was shown to inhibit the production of noradrenaline in rat brain tissue and is used as a model for studying genetic polymorphism. Techniques such as nuclear magnetic resonance spectroscopy, infrared spectroscopy, and X-ray crystallography have been used to investigate the structure and reactivity of 4-chloro-3-fluorobenzaldehyde.

2,3,5-Trichlorobenzaldehyde is a chemical compound that has been shown to have anticancer and apoptotic effects. It inhibits the growth of bacteria by chelating iron ions and inhibiting bacterial dna synthesis. 2,3,5-Trichlorobenzaldehyde has also been shown to inhibit the growth of cancer cells in culture in an experimental study. This chemical has been used as a substrate for nmr spectroscopy to study its functional groups and radical scavenging activities. 2,3,5-Trichlorobenzaldehyde can be synthesized from phenacyl chloride and benzaldehyde in the presence of hydrogen chloride gas. The carbonyl group in 2,3,5-trichlorobenzaldehyde may cause metabolic disorders such as diabetes mellitus or hyperglycemia.

Trityl chloride resin is a chemical compound that is used as a model system for the study of trifluoroacetic acid and its reactions. Trityl chloride resin is insoluble in water and has been used as a reaction solution for transfer reactions. It has been shown to be an effective ligand for many types of receptors, with binding constants ranging from 10 M-1 to 10 M-10. Trityl chloride resin can also be chiral, which means that it may exist in two forms that are mirror images of each other. The physiological effects of this compound are not well understood, but it has been shown to have an effect on coordination geometry.

Please enquire for more information about S-(-)-Nicotine-delta1’-(5’)-iminium diperchlorate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Endogenous heptapetide which causes vasodilation and has anti-hypertensive properties.

Undecafluorohexanoic acid is a perfluoroalkyl carboxylic acid that has been shown to disrupt steroidogenesis in vitro. It may be able to inhibit the transport of cholesterol, fats, and other lipids in cells, which causes disruption in steroidogenesis. This compound also has anti-cancer properties due to its ability to induce apoptosis and arrest cancer cell proliferation. Undecafluorohexanoic acid may also have developmental effects on animals because it can bind to estrogen receptors and disrupt the normal process of estrogen-mediated signaling pathways.

3-(2-Fluoroethoxy)Propanenitrile is a chemical with toxic properties. It is classified as a fluoroacetic acid and has been used in the production of other chemicals. Fluoroacetic acid is toxic to humans, showing signs of skin irritation, respiratory tract irritation, and kidney damage. 3-(2-Fluoroethoxy)Propanenitrile is not found naturally and has been sponsored by many companies.

Triethyloxonium tetrafluoroborate is an antimicrobial agent that inhibits the transfer of electrons from one molecule to another. It has been shown to be effective against methicillin-resistant Staphylococcus aureus and Mycobacterium tuberculosis. Triethyloxonium tetrafluoroborate binds to the bacterial enzyme, Jak1, which is involved in the formation of cytokines and interleukins. This binding inhibits the production of these molecules, leading to cell death by apoptosis. The use of triethyloxonium tetrafluoroborate as a research tool has facilitated its discovery as a potential anti-inflammatory drug for autoimmune diseases such as type 1 diabetes mellitus and rheumatoid arthritis. Triethyloxonium tetrafluoroborate can be used to inhibit amide synthesis, which may have applications in the study of carbohydrate chemistry and nitrogen atoms in biological systems. This compound has also been used

2,3-Bis(bromomethyl)quinoxaline is a nitrogenous heterocyclic compound that has a coordination geometry of square planar. It has been used as an inhibitor for the protein p21 and the nucleophile in palladium complexes. 2,3-Bis(bromomethyl)quinoxaline is also a model system for studying reaction mechanisms and chemical structures. The electron density map of the compound was obtained by X-ray crystal structure analysis. The reaction mechanism of this molecule is proposed to be through a chelate ring cross-coupling process.