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Methyl 2,5,6-Trichloropyrimidine-4-carboxylate,Cas:89284-85-5: A Versatile Chemical Compound

Methyl 2,5,6-Trichloropyrimidine-4-carboxylate 89284-85-5: A Versatile Chemical Compound | Available at Finetech Industry LimitedIntroduction:Methyl 2,5,6-trichloropyrimidine-4-carboxylate is a chemical compound known for its versatility and wide-ranging applications. At FINETECH Industry Limited, we offer this compound to meet the diverse needs of industries. This article provides an overview of methyl 2,5,6-trichloropyrimidine-4-carboxylate, including its structure, synthesis methods, and potential applications, highlighting how you can contact us for your requirements.Chemical Structure:Met [...]

Nov 19, 2024 ---- News 328 Views Read More

1,4-Dibenzyloxybenzene: A Versatile Compound for Rubber Production and Industrial Antioxidant Applications

1,4-Dibenzyloxybenzene, also known as Antioxidant DBH or Hydroquinone dibenzyl ether, is a chemical compound with the molecular formula C20H18O2 and CAS number 621-91-0. It is a white to off-white powder that is sparingly soluble in ethanol, gasoline, and water, but soluble in acetone, benzene, and chlorobenzene. This compound is primarily used as a moderate-level antioxidant, particularly in the manufacturing of sponge rubber products. It is valued for its ability to prevent discoloration and pollution, making it suitable for long-term exposure to sunlight. In the latex industry, it has signi [...]

Nov 19, 2024 Product News 328 Views Read More

Idarubicin: Mechanism of Action, Side Effects, and Clinical Applications in Cancer Treatment

Idarubicin 57852-57-0is a potent chemotherapy drug belonging to the anthracycline class, primarily used in the treatment of various types of cancer, including acute myeloid leukemia (AML) and acute lymphocytic leukemia (ALL). Its mechanism of action, side effects, and clinical applications make it a crucial component of cancer treatment regimens.Mechanism of Action:Idarubicin exerts its anticancer effects by interfering with the DNA and RNA synthesis of cancer cells. It does so by intercalating between DNA base pairs, inhibiting the activity of topoisomerase II enzyme, and generating free radi [...]

Nov 19, 2024 Product News 398 Views Read More