Halogénures organiques

<p>17b-Acetoxy-2a-bromo-5a-androstanone is a chemical that belongs to the class of hydroxysteroids. It is a potent aromatization agent and has been shown to increase the production of estradiol in human placental tissue. 17b-Acetoxy-2a-bromo-5a-androstanone also has been shown to be a potent inhibitor of bacterial growth, with an MIC90 of 0.1 micrograms per milliliter.</p>

<p>Chloranilic acid is a thermally unstable compound that undergoes a number of reactions with the addition of heat. It reacts with nitrogen atoms to form amides, nitriles, and nitro compounds. Chloranilic acid also reacts with polymerases to form stable complexes. The proton at the center of the chloranilic acid molecule is lost when it forms an acid complex. This reaction occurs in aqueous solution as well as in biological systems, where it is used for hydrogen bonding interactions. The stable complexes that are formed by chloranilic acid have been shown to have biological properties such as antimicrobial activity, antiviral activity, and antifungal activity.</p>

<p>Please enquire for more information about 5-({[2-(4-Chlorophenyl)-1,3-oxazol-4-yl]methyl}thio)-1,3,4-thiadiazol-2-amine 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 6-Bromo-3-phenylquinazoline-2,4(1H,3H)-dione 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 4-Methoxy-N-methylbenzylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 5-bromo-2-iodobenzoate (MIB) is a thiourea that inhibits the enzyme activity of thioredoxin reductase. It has been shown to inhibit the proliferation of cancer cells in vitro and in vivo, as well as induce apoptosis. MIB has also been shown to have a potent antiproliferative effect on various cancer cell lines and other natural compounds. MIB is an efficient anticancer agent with a high quantum efficiency, which may be due to its ability to scavenge free radicals. MIB can also be used to increase the yields of other natural compounds.</p>

<p>1,3-Bis(3,3,3-trifluoropropyl)-1,1,3,3-tetramethyldisilazane is a dielectric with a low dielectric constant and high hydrophobicity. It can be used as a self-assembled monolayer for reducing the contact angle on hydrophobic surfaces. 1,3-Bis(3,3,3-trifluoropropyl)-1,1,3,3-tetramethyldisilazane has been used in transistors to increase the conductivity of pentacene monolayer.</p>

<p>Please enquire for more information about 5-Bromo-1H-indazol-3-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Arachidonoyl chloride is a chemical compound that belongs to the group of amides. It is used in biological studies for receptor binding and enzyme activities. Arachidonoyl chloride has been shown to inhibit insulin sensitivity by inhibiting the phosphorylation of tyrosine residues on insulin receptors, which are necessary for glucose transport into cells. The acyl chain of arachidonoyl chloride has a polyunsaturated fatty acid structure with two double bonds, which is important for its activity on the 2-arachidonoylglycerol (2-AG) pathway. The activation energy of arachidonoyl chloride is not yet known.</p>

<p>Silver trifluoromethanesulfonate (AgOTf) is a precursor in the synthesis of alpha-bromo-m-tolunitrile. It is a colorless, odorless solid that can be prepared by the reaction of silver ions with bromine and toluene in an aqueous medium. The profile of AgOTf has been studied by titration method and it has been shown to have an oxadiazole group. This molecule also has anticancer activity against cancer cells. Alpha-Bromo-m-tolunitrile is currently being investigated for its potential use as a drug candidate for the treatment of cancer, with particular interest in the inhibition of angiogenesis and metastasis.</p>

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

<p>5-Bromo-1H-indole-2-carboxylic acid methyl ester is a drug that belongs to the class of carboxylates. It has been shown to inhibit the growth of tumor cells in vitro and in vivo. The antitumor activity of this compound may be due to its ability to stabilize planar indole moieties, which are cytotoxic. 5-Bromo-1H-indole-2-carboxylic acid methyl ester interacts with other molecules through intermolecular interactions and can form an indole ring system that has a trifluoromethyl group and a carboxylate group in its structure.</p>

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

<p>Chromonar hydrochloride is a non-steroidal anti-inflammatory drug that is used to treat the symptoms of bowel disease. It relieves pain and reduces inflammation by blocking the production of prostaglandins. Chromonar hydrochloride may also be used to reduce blood pressure and relieve chest pain caused by heart disease. It has been shown to have cardioprotective effects in experimental models. Chromonar hydrochloride is metabolized by cytochrome P450 enzymes, which are involved in the synthesis of proteins, as well as other enzymes that maintain the integrity of DNA and RNA molecules. Chromonar hydrochloride can also cause an allergic reaction if taken with nitrous oxide.</p>

<p>1-Bromo-2,4,5-trifluorobenzene is a liquid crystal that can be used to synthesize amides in an asymmetric synthesis. It has been shown to react with nucleophiles such as β-amino acids or chloride ions to form an amide. This compound is also thermally stable and can be stored at room temperature. The structural formula of 1-bromo-2,4,5-trifluorobenzene is C6H3BrF3. Functional groups present on this molecule include a bromine atom (Br), three hydrogen atoms (H) and two fluorine atoms (F).</p>

<p>Please enquire for more information about Methyl 2-amino-4,6-dichloropyridine-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 4,6-dichloronicotinate (EDCN) is a hybrid drug that can be used as a clinical drug for the treatment of cancers. EDCN has been shown to have an antiproliferative effect in hematopoietic cells and tumor cells. It is also able to inhibit tyrosine kinase activity and cellular proliferation by inducing apoptosis. EDCN has been shown to be a potent inhibitor of cancer cell growth in vitro and in vivo, with IC50 values ranging from 1 to 10 μM. This drug is active against leukemia, lymphoma, breast cancer, prostate cancer, colorectal cancer, and other cancers that are sensitive to inhibition by tyrosine kinase inhibitors. EDCN binds reversibly to DNA with high affinity and specificity through hydrogen bonding interactions between the nucleobases on its aromatic ring system and the purine bases on dsDNA. This binding inhibits transcription by blocking access of RNA polymerase II to DNA templates</p>

<p>Please enquire for more information about [2-(Methylsulfinyl)ethyl]amine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>7-Amino-4-(trifluoromethyl)coumarin is a coumarin derivative that has been used as a fluorescence probe for the study of enzyme activities. It can be used as a potential biomarker for autoimmune diseases, and has also been shown to have tyrosine kinase domain binding activity. 7-Amino-4-(trifluoromethyl)coumarin can bind to the hydroxyl group in tyrosine residues with high affinity, and binds to the nitrogen atoms in protein kinases with low affinity. This compound is able to form intermolecular hydrogen bonds and steric interactions with peptide hormones.</p>

<p>2-Bromo-4-methylacetophenone is a synthetic compound that inhibits bacterial growth through acetylation of the aromatic ring. It is used in the synthesis of imidazolidinones, which are a class of antibacterial drugs. 2-Bromo-4-methylacetophenone has shown inhibitory activity against MCF-7 breast carcinoma cells and mononuclear cells. It also has been synthesized from phenacyl bromide and potassium carbonate in anhydrous conditions. The crystal system for 2-bromo-4-methylacetophenone is tetragonal with space group P42/mnm.</p>