methyl 4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylate

Methyl-4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid ester, this is an organic compound. To know its chemical structure, please listen to me in detail.
In terms of its name, "methyl" is an alkyl group containing one carbon, represented by "-CH". "4-hydroxy" indicates that there is a hydroxyl group (-OH) at the 4th position of the isoquinoline ring. "1-methyl", that is, at the 1st position of the isoquinoline ring, is also connected by a methyl group. " 7-Phenoxy "means that at the 7th position of the isoquinoline ring, a phenoxy group (-O-phenyl) is attached, and the phenyl group is the remaining part of the benzene ring after removing a hydrogen atom." Isoquinoline "is a class of nitrogen-containing heterocyclic compounds with a unique cyclic structure, which is formed by fusing a benzene ring with a pyridine ring." 3-carboxylate "means that at the 3rd position of the isoquinoline ring, there is a carboxylic acid ester group. The carboxylate group is usually represented by -COOR, where R is methyl (-CH).
In summary, the chemical structure of this compound is as follows: the isoquinoline ring is the core, with methyl and hydroxyl groups at the 1st and 4th positions, phenoxy groups at the 7th position, and carboxylic acid methyl ester groups at the 3rd position. In its structure, the isoquinoline ring provides a rigid skeleton, and each substituent gives it unique physical and chemical properties. Hydroxyl groups can participate in the formation of hydrogen bonds, which affects the solubility and reactivity of the compound; phenoxy groups increase the hydrophobicity and steric resistance of the molecule; methyl and carboxylate groups also have significant effects on the properties and reactivity of the compound.

Methyl-4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid ester, which is an organic compound. Its physical properties are as follows:
Viewed at room temperature, it is either solid or crystalline, and its color is colorless and transparent, or slightly colored, which varies due to differences in impurities or crystal forms. Its melting point is crucial for identification and purity determination, but the exact value needs to be determined experimentally and accurately.
In terms of solubility, it varies from organic solvents. Common organic solvents such as ethanol, acetone, dichloromethane, etc., may be soluble, because the molecular structure contains specific functional groups, and interact with organic solvents. However, in water, due to its dominant hydrophobic groups, the solubility may be extremely low or nearly insoluble.
The boiling point is also a key physical property. However, when heated or decomposed, it is difficult to determine the exact boiling point.
The density is related to the relationship between the mass and volume of the substance. Although the exact density value needs to be measured experimentally, it is inferred from the structure and similar compounds that its density may be higher than that of water.
In addition, the compound may have a certain degree of hygroscopicity, and in humid environments, or absorb water vapor in the air, causing its own state to change. Its smell may be weak, or it may have a special organic smell. However, the exact smell also needs to be actually sensed by smelling.
In summary, the physical properties of methyl-4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid esters are significantly affected by the structure, functional groups and external environment, and the exact properties need to be determined by experiments.

Methyl-4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid ester, this is an organic compound. Its main uses, let me tell you in detail.
In the field of medicine, such compounds may have unique medicinal potential. The isoquinoline structure is commonly found in many bioactive molecules, or can interact with specific targets in organisms. Or it can regulate cell physiological processes and be beneficial to the treatment of certain diseases. For example, it may act on specific enzymes or receptors, affect cell signal transduction pathways, and may become a leading compound for innovative drugs for the treatment of cardiovascular diseases, nervous system diseases, and other diseases. Pharmaceutical developers can optimize their pharmacological properties by modifying their structures, such as enhancing their efficacy and reducing toxic and side effects.
In the field of materials science, it may serve as a building block for functional materials. Due to its special chemical structure, it may endow materials with unique electrical, optical or thermal properties. For example, in organic optoelectronic materials, it may participate in the construction of conjugated systems, which affect the luminescence properties and charge transfer efficiency of materials, providing the possibility for the preparation of new Light Emitting Diodes and solar cell materials.
In the field of organic synthetic chemistry, this compound can be used as a key intermediate. With its multiple reactivity check points, it can derive complex organic molecules with diverse structures through various organic reactions. Chemists can use this to construct more valuable natural product analogs or new functional molecules, expand the structural diversity of organic compounds, and promote the development of organic synthesis chemistry.
In summary, methyl-4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylate has potential important uses in many fields such as medicine, materials science, and organic synthesis, providing opportunities for scientific research and technological innovation.

The method of synthesizing methyl 4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid ester is quite complicated, and it is necessary to choose the suitable one according to various conditions. One method is to take the corresponding phenols and halides first, and carry out nucleophilic substitution reaction under the catalysis of bases to form phenoxy intermediates. In this step, the type and dosage of bases need to be carefully selected, and the reaction temperature and time should be controlled, so that higher yields can be obtained. < Br >
Then, the obtained intermediate and the appropriate nitrogen-containing heterocyclic precursor are promoted to cyclize under the action of suitable solvents and catalysts to construct the skeleton of isoquinoline. Among them, the polarity of the solvent and the activity of the catalyst have a great influence on the reaction process and the purity of the product.
Or there are other methods, the desired substituents can be gradually introduced from the starting material with specific functional groups through multi-step reactions. For example, compounds containing carboxyl and hydroxyl groups are prepared first, and then methylation, phenoxylation and cyclization are carried out in sequence. Each step of the reaction requires fine regulation of the reaction conditions to avoid the generation of side reactions and maintain the purity of the product.
Furthermore, after the reaction is completed, the separation and purification of the product is also crucial. High-purity methyl 4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylate can be obtained by column chromatography, recrystallization, etc. to remove its impurities and improve its purity. In short, the synthesis of this compound requires a deep understanding of the principle of organic reaction and a detailed investigation of the conditions of each step.

Methyl-4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid ester, this product is in the market price range, and it is difficult to break. The price is not static, but is affected by many factors.
First, it is related to the purity of this product. If the purity is high, it is almost flawless, and its price must be high; if it contains impurities and is slightly flawed, the price should be low. Such as the ancient beautiful jade, the price of flawless is heavy, and the price of flawless is slightly inferior.
Second, the amount of output is also the key. If the output of this product is scarce, the supply is in short supply, just like a rare treasure, the price will be expensive; if the output is full, the supply exceeds the demand, and the price will naturally decline, just like ordinary things.
Third, the trend of market demand has a great impact. If everyone needs it nowadays, it is widely used, and the demand is strong, the price will rise; if the demand is low, few people will ask about it, and the price will be difficult to vibrate.
Fourth, the difficulty of preparation is also relevant. If the preparation method is complicated, it consumes a lot of manpower and material resources, and the cost is high, the price is not cheap; if the preparation is simple, the cost is low, and the price will become easy.
Therefore, in order to determine the exact price range of methyl-4-hydroxy-1-methyl-7-phenoxyisoquinoline-3-carboxylic acid ester in the market, it is necessary to carefully consider the above factors and comprehensively consider them before obtaining a more accurate judgment. However, it is difficult to directly state its specific price range.