Organic Halides

<p>4-(4-Chlorophenyl)-5-methylthiazol-2-amine is a potent inhibitor of osteoblast function. It inhibits the production of interleukin-6, which is a cytokine that regulates inflammation and bone resorption. 4-(4-Chlorophenyl)-5-methylthiazol-2-amine also has an inhibitory effect on thiourea, a natural compound that is formed in the body during the process of purine metabolism. This compound is synthesized by methylation of 4-(4-chlorophenyl)thiazole (TCP). The residuals from this synthesis are excreted in urine as 4-(4-chlorophenyl)thiazol (TCT).</p>

<p>Please enquire for more information about N-(3,5-Bis(trifluoromethyl)phenyl)-2-chloropropanamide 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-((4-Acetylphenyl)amino)-2-chloro-5-methylcyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Please enquire for more information about 2-(6-chlorobenzimidazol-2-yl)-3-hydroxyinden-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(3-Chlorophenyl) thiourea is a curcumin analog that has been shown to inhibit the epidermal growth factor (EGF) receptor. It is synthesized from 1,2-dichlorobenzene and urea in a two-step process. The anhydrous potassium carbonate is first converted to the potassium salt with an acid chloride. The second step is the reaction of this salt with urea in the presence of excess anhydrous potassium carbonate. This product has been shown to be effective against cancer cells and may be used as a potential anticancer agent for treatment of skin cancer. 1-(3-Chlorophenyl) thiourea inhibits EGF receptor by binding to it and preventing its activation, which prevents cell proliferation and reduces tumor size.</p>

<p>Please enquire for more information about 2-Chloro-N-(3-chloro-4-cyanophenyl)propanamide 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 N-(4-tert-Butylphenyl)-2-chloropropanamide 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 N-(4-Acetylphenyl)-3-chloropropanamide 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 N-(2-bromo-4-fluorophenyl)thiourea including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Iodoisatin is a cross-coupling agent that has an inhibitory effect on tumor tissue. It is also used for the synthesis of conjugated drugs and pharmacological research. 5-Iodoisatin, which forms a ternary complex with copper and iodide, inhibits the growth of colorectal carcinoma cells by interfering with their DNA replication and protein production. 5-Iodoisatin can be converted to its active form through the formation of a ternary complex with copper and iodide ions. This inhibition is due to its ability to interact with DNA, RNA polymerase, and other proteins involved in transcription, translation, and replication processes. 5-Iodoisatin is metabolized through conjugation with glucuronic acid or sulfate in the liver; it binds to human mitochondrial DNA and can enter cells via passive diffusion. The carbonyl group in this drug may play an important role in its interaction with cancer cells.</p>

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<p>Please enquire for more information about (4-(4-bromophenyl)(2,5-thiazolyl))-3-pyridylamine 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 N-(2-Isopropylphenyl)-2-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Please enquire for more information about methyl 3-(4-bromophenyl)-2-nitrileprop-2-enoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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<p>2-(4-Chlorobenzenesulphonyl)acetonitrile is a reactive chemical that is synthesized from chloroform and acetonitrile. It can be used to synthesize various medicines such as analgesics, muscle relaxants, and x-ray contrast agents. 2-(4-Chlorobenzenesulphonyl)acetonitrile has minimal effects on the human body and is not known to cause any major health problems. It is metabolized in the liver by oxidation of the methyl group to form 4-chlorobenzene sulfonic acid, which is excreted through urine. The chlorine atom in this molecule has a trigonal bipyramidal geometry with a bond length of 1.82 Å, which can be seen in x-ray crystallography studies.</p>

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<p>Please enquire for more information about N-(3,5-bis(trifluoromethyl)phenyl)-2-pyrimidin-2-ylthioethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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