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The Instruction of ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE in Chemical Industry
Introduction:
Ethyl 4-hydroxy-6-methoxyquinoxaline-3-carboxylate, commonly referred to as ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE, is a chemical compound that is used in various applications in the chemical industry.
The chemical formula for this compound is C14H14O5.
It is a white crystalline solid with a molecular weight of 254.
29 g/mol.
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE is soluble in water and is highly reactive.
Chemical Structure:
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE is a quinoline derivative, which is a type of organic compound that contains a quinoline ring.
The quinoline ring is a bicyclic organic compound that contains two benzene rings fused together.
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE has a unique chemical structure that is characterized by the presence of a hydroxyl group, a methoxy group, and a carboxylate group.
The presence of these functional groups makes ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE highly reactive and versatile in various applications.
Applications:
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE is used in various applications in the chemical industry.
One of its most common applications is in the production of pharmaceuticals.
The compound is used in the synthesis of various drugs and medicines due to its unique chemical structure and reactivity.
Another application of ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE is in the production of dyes and pigments.
The compound is used as a starting material in the synthesis of various dyes and pigments due to its ability to impart specific colors to the final product.
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE is also used in the production of plastics and other synthetic materials.
The compound is used as a catalyst in the production of polyesters, which are used in the production of plastics and other synthetic materials.
Preparation:
ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE can be prepared by various methods.
One of the most common methods is through the reaction of 4-hydroxy-6-methoxyquinoline-3-carboxaldehyde with ethyl bromide in the presence of a Lewis acid catalyst, such as aluminum chloride.
The reaction involves the condensation of 4-hydroxy-6-methoxyquinoline-3-carboxaldehyde with ethyl bromide in the presence of the Lewis acid catalyst.
The reaction results in the formation of ETHYL 4-HYDROXY-6-METHOXYQUINOLINE-3-CARBOXYLATE, which is a white crystalline solid.
Safety and