Organic Halides

<p>4-Bromo-6-chloropyridazin-3(2H)-one is a glycosylation inhibitor and nucleoside analog that can be used in the treatment of cancer. It inhibits the synthesis of deoxyribonucleotides from ribonucleotides by binding to the enzyme ribonucleotide reductase, which catalyzes the conversion of ribonucleotides to deoxynucleotides. 4-Bromo-6-chloropyridazin-3(2H)-one has been shown to inhibit glycosylation in rat liver cells. This drug also inhibits acetone and glycosidation, which are reactions that produce glucose from amino acids or carbohydrates. The crystallization process is also inhibited by this drug because it prevents the formation of nucleoside crystals, which are involved in DNA replication and cell division.</p>

<p>2-Bromo-6-methylpyridine-3-carboxaldehyde (BMPCA) is a pharmacological agent that belongs to the group of antagonists. It has been shown to be a potent antagonist at the NMDA receptor and may be used for treating neuropathic pain. BMPCA also has been shown to have competitive inhibition at the naphthyridine receptor, which may allow it to act as an antagonist or an agonist depending on its binding site. The regioisomeric analogs of BMPCA are 2-(2,5-dichloropyridyl)-6-methylpyridine-3-carboxaldehyde and 2-(2,5-dimethylpyridyl)-6-methylpyridine-3-carboxaldehyde. These analogs have been shown to inhibit the growth of tumor cells in vitro and in vivo.</p>

<p>Trifluoroacetate salt</p>

<p>Please enquire for more information about H-Ala-2-chlorotrityl resin (200-400 mesh) (Low Substitution) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about GLP-1 (7-36)-Lys(biotinyl) amide (human, bovine, guinea pig, mouse, rat) trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>Diphenyliodonium chloride is a synthetic chemical that binds to DNA and inhibits the synthesis of proteins. It also has been shown to inhibit the growth of Gram-positive bacteria, including Methicillin-resistant Staphylococcus aureus (MRSA) and Streptococcus pneumoniae, but not Gram-negative bacteria such as Escherichia coli or Pseudomonas aeruginosa. Diphenyliodonium chloride is used in a variety of ways, including as an antimicrobial agent for the prevention of microbial contamination in pharmaceuticals and cosmetics.</p>

<p>Please enquire for more information about Fmoc-L-Lys[Oct-(otBu)-Glu-(otBu)-AEEA-AEEA]-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Tyr-Amyloid P Component (27-38) amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>A dehydration agent.  Also called Martin Sulfurane Dehydrating agent</p>

<p>2-Chloro-4-hydroxybenzyl alcohol is an organic compound that has been shown to be soluble in aqueous alkali metal solutions, but insoluble in water. It is also insoluble in polymer solvents such as acetone and ethyl ether. 2-Chloro-4-hydroxybenzyl alcohol is a sugar alcohol with 3 hydroxyl groups. The molecule has a molecular weight of 150.17 g/mol, melting point of -123°C (-198°F), boiling point of 179°C (354°F), and refractive index of 1.5774 at 20°C (68°F). This chemical can be used in the synthesis of polyhydric alcohols such as glycerol or hexanol. 2-Chloro-4-hydroxybenzyl alcohol is not soluble in hydrochloric acid, benzene or chloroform, and does not react to form any es</p>

<p>Please enquire for more information about Mca-Pro-Leu-Ala-Nva-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</p>

<p>Please enquire for more information about 2-Chloromethyl-3,5-dimethylpyridin-4-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Bromopyridazine is a dechlorinated derivative of pyridazine that has been used as an agrochemical. 3-Bromopyridazine can be synthesized by aminocarbonylation at the 3-position, which is a nucleophilic substitution reaction. It has been shown to yield high yields and to react with nucleophiles such as chlorine or heterocycles such as cinnoline. 3-Bromopyridazine can also be obtained by cross coupling of 2-bromoacetophenone with benzaldehyde and pyridine in the presence of copper. The resulting product is then reacted with sodium nitrite in hydrochloric acid to produce 3-bromopyridazine. This compound may have potential use as a chemical intermediate for other compounds, due to its chemical stability and its ability to undergo cross coupling reactions.</p>

<p>Imidazole trifluoromethanesulfonate is a compound that has been used as an ingredient in deionized water. It is also used to treat cardiovascular disorders, psychotic disorders, and metabolic disorders. Imidazole trifluoromethanesulfonate has been shown to reduce the production of hydrogen peroxide in the brain and prevent oxidative damage to DNA. This drug prevents the synthesis of imidazoline, which may be responsible for its effects on blood pressure and heart rate. Imidazole trifluoromethanesulfonate is metabolized by cytochrome P450 enzymes into a protonated form that can bind to viral polymerase and inhibit DNA synthesis. The drug also inhibits hepatitis B virus replication by binding to the NS5B polymerase protein essential for viral RNA synthesis.</p>

<p>Intermediate in the synthesis of dapagliflozin</p>

<p>2-Bromo-3-fluoroaniline is a reactive and nucleophilic compound that is synthesized by the reaction of aniline with bromine and sodium hydroxide. The drug development of 2-bromo-3-fluoroaniline has been hampered by its toxicity, but it has shown promising results in animal studies for the treatment of cancer. Mechanistic studies have demonstrated that 2-bromo-3-fluoroaniline causes cell death by reacting with DNA. This drug also acts as a prodrug to fluoroacetic acid, which inhibits cell proliferation by inhibiting protein synthesis.</p>

<p>Please enquire for more information about 2,3,6-Trifluorophenylacetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about ((R)-4-Hydroxy-4-methyl-Orn (FITC)7)-Phalloidin trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>13-mer connexin mimetic peptide, composed of residue numbers 63-75 of the first extracellular loop of connexin 43 (gap junction blocker), containing the SHVR amino acid motif.</p>

<p>2-Amino-1-phenylpropan-1-one hydrochloride is a chemical compound that can be used as an intermediate in the synthesis of ethyl formate. It is also a pharmaceutical intermediate, which is used to prepare triazine and alicyclic compounds. It has been shown to have potential use in the treatment of prostatic hypertrophy and heterocycle disorders. 2-Amino-1-phenylpropan-1-one hydrochloride has been found to be active in animals and humans and is not toxic to women or animals. This drug has shown no adverse effects on human health at doses up to 10 g/kg body weight.</p>

<p>5-Bromo-2-(trifluoromethoxy)benzaldehyde is a chemical that is used as a reactant in organic chemistry. It can be used as a building block for the synthesis of complex compounds, or as an intermediate in the preparation of fine chemicals. 5-Bromo-2-(trifluoromethoxy)benzaldehyde is also useful in research and development. It has been used to synthesize pharmaceuticals, pesticides, and other organic compounds.</p>

<p>Maxadilan trifluoroacetate salt is a low-potency drug that binds to the GABA receptor and affects the central nervous system. Maxadilan trifluoroacetate salt is structurally related to leishmaniasis, an infectious disease caused by protozoa of the genus Leishmania. Maxadilan trifluoroacetate salt has been shown to prevent the development of autoimmune diseases in mice, including systemic lupus erythematosus, experimental autoimmune encephalomyelitis, and collagen-induced arthritis. Maxadilan trifluoroacetate salt has also been shown to be effective against cutaneous lesions in mice infected with Leishmania major. The mechanism of action is not yet known but may be due to its ability to influence mitochondrial membrane potential or fatty acid metabolism.</p>

<p>Please enquire for more information about AQEE-30 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Adrenomedullin (porcine) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about APL1b28 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Fluoroanisole is an organic compound that is used in organic synthesis as a chiral auxiliary. It has been shown to inhibit the growth of cancer cells by binding to nucleophilic sites on the cell and preventing the formation of new proteins. 2-fluoroanisole is synthesized through a two-step process that begins with the asymmetric synthesis of the desired chiral molecule using a chiral catalyst and deuterium isotope. The second step involves converting 2-fluoroanisole into its more stable form, dodecanedioic acid, by treating it with hydrochloric acid or trifluoroacetic acid. The structural analysis of this molecule revealed that it contains two nucleophilic substitutions, which are likely responsible for its inhibitory properties.</p>

<p>Please enquire for more information about (D-His2,D-Trp6)-LHRH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>2-Bromo-1-indanol is an industrial solvent used in the production of dyes, pigments, perfumes, pharmaceuticals, and other organic compounds. It is a chiral compound with two stereoisomers (R and S) that have different properties. The R isomer has a hydroxyl group on the 2 position of the indane ring, while the S isomer does not. The industrial process involves recycling of 2-bromo-1-indanol from the reaction mixture. This process can be monitored using mass spectrometric detection for bromine and hydrogen ions released during hydrolysis.<br>2-Bromo-1-indanol can be used to synthesize methoxybenzaldehyde with high regioselectivity, which can then be used to make some drugs such as amphetamine and methamphetamine.</p>

<p>Please enquire for more information about (Gly14)-Humanin (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>T-type calcium channel inhibitor</p>

<p>Please enquire for more information about APL1b25 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>9,9-Bis[4-(2-acryloyloxyethyloxy)phenyl]fluorene is a monofunctional, monomeric and optical initiator. It is a bifunctional molecule that can polymerize with other molecules to form polyesters. 9,9-Bis(4-acryloyloxyethyloxyphenyl)fluorene is also an element which can polymerize with other molecules to form polymers. This compound has been used in experiments for the study of optical properties such as refractive index and birefringence. The compound is liquid crystal and has been used for the study of liquid crystals as well.</p>

<p>D-Pen 2,p-chloro-Phe4,D-Pen 5)-Enkephalin H-Tyr-D-Pen-Gly-p-chloro-Phe-D-Pen (Disulfide bond) is a peptide that belongs to the family of opioid drugs. It has low potency and is used in pharmacological studies as a nonselective antagonist of δ-, μ-, and κ-(kappa) receptors. This drug blocks pain by binding to the same receptor sites that are activated by endogenous opioids and has been shown to be effective against both inflammatory and neuropathic pain. DPDPE has also been shown to have a high safety profile with minimal side effects.</p>

<p>MeOSuc-Ala-Ala-Pro-Ala-chloromethylketone is a peptidyl substrate for the enzyme carboxypeptidase A. This substrate has a high specificity for carboxypeptidase A and does not bind to other enzymes such as carboxypeptidase B, D, or L. The hydrophobic nature of this substrate has been shown in both hamsters and macaques. MeOSuc-Ala-Ala-Pro-Ala-chloromethylketone also shows cardiovascular effects in both animal models. It is possible that this effect is due to the proteolytic activity of the enzyme. More research needs to be done to identify the sequence of this peptide and how it may affect humans.</p>

<p>4-Methoxy-3-(trifluoromethyl)benzoic acid is a useful scaffold that can be used as a building block for the synthesis of complex compounds. It has been shown to react with various reagents and is a versatile building block that can be used in organic synthesis. 4-Methoxy-3-(trifluoromethyl)benzoic acid is a high quality chemical and has been classified as speciality chemicals. This product is also known by the CAS number 213598-09-5.</p>

<p>4-Chloro-2-(trifluoromethoxy)aniline is a fine chemical that is used as a building block in the synthesis of other chemicals, such as pharmaceuticals and agrochemicals. It is also used in research as a reagent for organic synthesis and as a speciality chemical. 4-Chloro-2-(trifluoromethoxy)aniline has versatile applications in the manufacture of complex compounds, intermediates, and scaffolds.</p>

<p>2,3,4-Trichloro-5-fluorobenzoic chloride (TCFB) is a sulfuryl chloride that is used as a herbicide. TCFB is hydrolyzed by carboxylates in the soil to form formic acid and hydrochloric acid. The hydrolysis of TCFB makes it selective for the roots of plants. TCFB can also be chlorinated to regenerate the acid and then recycled. Hydrolyzing TCFB allows it to be selectively applied on plant roots without affecting any other part of the plant. The presence of chlorine in this compound allows for its use as an insecticide and fumigant.</p>

<p>2-(2-Bromoethyl)-1,3-dioxolane is a synthetic chemical compound that is used for the asymmetric synthesis of fatty acids. It can be prepared by the cross-coupling reaction of ethyl formate with bromoethane and copper(II) acetate in trifluoroacetic acid. The reaction produces an unsymmetrical product with two aldehyde groups and two halides on each side of the molecule. It can also be prepared by the reaction of 2-bromoethanol with sodium formaldehyde sulfoxylate and sodium methoxide in methanol. This process produces a symmetrical molecule with one aldehyde group on each side of the molecule. 2-(2-Bromoethyl)-1,3-dioxolane has been shown to have anti-cancer properties in carcinoma cell lines.</p>

<p>Please enquire for more information about Cecropin B (free acid) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about HCV NS4A Protein (22-33) (FDA strain) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Thr-Ala-Pro-Arg-Atrial Natriuretic Factor (1-28) (human, bovine, porcine) trifluoroacetate salt is a peptide hormone that regulates blood pressure by causing the kidneys to excrete sodium and water. It is used as a model system for studying the physiological effects of urodilatin and has been shown to inhibit the cyclase enzyme. Thr-Ala-Pro-Arg-Atrial Natriuretic Factor (1-28) (human, bovine, porcine) trifluoroacetate salt may also have an antihypertensive effect through its ability to reduce levels of natriuretic peptides in plasma. This drug is also being investigated as a possible treatment for congestive heart failure. The small molecular weight makes it suitable for use as a natriuretic or antihypertensive drug with minimal side effects.</p>

<p>Biotinyl-Substance P trifluoroacetate salt Biotinyl-Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2 trifluoroacetate salt is a biotin conjugated Substance P analog. It is designed to bind to the amino acid sequences in the brain that are responsible for controlling and regulating pain. The drug's amino acid sequence was designed by accessing databases of amino acid sequences from all known organisms. The drug is administered as a sequence of cassettes, each containing an acid molecule that can be transferred to cells through nucleotide transfer.</p>

<p>Please enquire for more information about GRPP (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about uPAR (84-95) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(2R,3S)-3-Amino-2-hydroxy-3-phenylpropanoic acid hydrochloride is an organic compound that is used in the manufacture of taxol, an anticancer drug. It is synthesized by reacting chloroacetic acid with a metal hydroxide, such as sodium hydroxide or potassium hydroxide. The reaction proceeds spontaneously to form the enantiomerically pure (2R,3S) form and unreacted (2S,3R) form. The (2R,3S) enantiomer has been found to be more reactive than the (2S,3R) form. Quaternary ammonium salts are formed when the (2R,3S) enantiomer reacts with quaternary ammonium compounds such as benzyltrimethylammonium chloride. This compound can also be used in catalytic reactions to produce drugs such as carbapenems and pen</p>

<p>Levomilnacipran is a serotonin-norepinephrine reuptake inhibitor (SNRI) that is used for the treatment of major depressive disorder and fibromyalgia. It has been shown to have antidepressant effects in patients with major depressive disorder and fibromyalgia. Levomilnacipran inhibits the reuptake of serotonin and norepinephrine by blocking the transporter proteins in these neurotransmitter pathways, increasing their availability to interact with receptors in the brain. Levomilnacipran also has been found to inhibit aminotransferase activity, which may be responsible for its hepatotoxicity.</p>

<p>2-Aminoethanesulphonamide monohydrochloride is a perovskite with a hexagonal shape. It has been shown to interact with the pharmacophore of the enzyme cytochrome P450, and it has been optimized for the reaction by altering its structure. This product is soluble in gaseous form, but can also be used as a solid. 2-Aminoethanesulphonamide monohydrochloride has an absorption maximum at 325 nm and emits fluorescence at 420 nm. It is used in devices that detect ionizing radiation.</p>

<p>MPLP(139-151) is a peptide that is derived from the myelin proteolipid protein (PLP). MPLP(139-151) has been shown to inhibit macrophage inflammatory in vitro and brain inflammation in vivo. The inhibition of macrophages was mediated by the induction of apoptosis and inhibition of NF-κB. MPLP(139-151) also induced regression of experimental autoimmune encephalomyelitis in mice, which suggests that it might be useful as a therapeutic agent for multiple sclerosis or other inflammatory diseases.</p>