3s 2 R R 3r 1 2 3 4 Tetrahydro 6 7 Dimethoxy 2 2 1 Ethoxycarbonyl 3 Phenylpropyl Amino 1 Oxopropyl 3 Isoquinolinecarboxylic Acid Monohydrochloride
Quinoline Thiophene Imidazole Thiazole
(3S-(2(R*(R*)),3R*))-1,2,3,4-Tetrahydro-6,7-dimethoxy-2-(2-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-1-oxopropyl)-3-isoquinolinecarboxylic acid monohydrochloride
Chemical Name (3S-(2(R*(R*)),3R*))-1,2,3,4-Tetrahydro-6,7-dimethoxy-2-(2-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-1-oxopropyl)-3-isoquinolinecarboxylic acid monohydrochloride
FAQ

What is the chemical structure of the compound (3S- (2 (R * (R *)), 3R *)) -1,2,3,4-Tetrahydro-6,7-dimethoxy-2- (2- ((1- (ethoxycarbonyl) -3-phenylpropyl) amino) -1-oxopropyl) -3-isoquinolinecarboxylic acid monohydrochloride?

This is the chemical structure analysis of (3S- (2 (R * (R *)), 3R *)) -1,2,3,4-tetrahydro-6,7-dimethoxy-2 - (2 - ((1 - (ethoxycarbonyl) -3 -phenylpropyl) amino) -1 -oxypropyl) -3 -isoquinoline carboxylic acid monohydrochloride.

The name of this compound contains a multifunctional group, and isoquinoline carboxylic acid is the parent structure. A side chain with a specific chiral carbon attached at the 3-position, which has a complex chiral label (3S- (2 (R * (R *)), 3R *)), indicating a special arrangement of the chiral configuration of the carbon at this position. 1, 2, 3, 4-tetrahydro characterizes the partial hydrogenation of the isoquinoline ring, and 6, 7-dimethoxy shows that the benzene ring has methoxy substitution at the 6 and 7 positions.

2-position side chain complex, (2 - ((1 - (ethoxycarbonyl) -3 -phenylpropyl) amino) -1 -oxopropyl), composed of ethoxycarbonyl, phenylpropyl, amino, carbonyl, etc., and connected to each other. The whole molecule forms a monohydrochloride, that is, a salt with a molecule of hydrogen chloride. Therefore, its chemical structure is drawn, with isoquinoline carboxylic acid as the core, arranged in sequence according to the position and connection of each substituent, and the atoms are connected according to the valence bond rule. The unique three-dimensional spatial structure of this compound is in line with the chemical composition and configuration indicated by its complex naming.

(3S- (2 (R * (R *)), 3R *)) -1,2,3,4-Tetrahydro-6,7-dimethoxy-2- (2- ((1- (ethoxycarbonyl) -3-phenylpropyl) amino) -1-oxopropyl) -3-isoquinolinecarboxylic monoacid hydrochloride What are the main physical properties?

(3S- (2 (R * (R *)), 3R *) - 1,2,3,4 - tetrahydro - 6,7 - dimethoxy - 2 - (2 - ((1 - (ethoxycarbonyl) - 3 - phenylpropyl) amino) - 1 - oxopropyl) - 3 - isoquinoline carboxylic acid monohydrochloride, this is an organic compound. Its main physical properties are as follows:
Viewed at room temperature and pressure, or white to off-white crystalline powder, because many organic hydrochloride compounds with similar structures are in this state, such as some drug hydrochloride salts containing benzene rings and heterocycles.
Smell, or have a weak special smell, organic compounds have a unique smell, but because the structure contains multiple methoxy groups, benzene rings and other groups, the smell is not pungent and strong, but relatively weak.
When it comes to solubility, because it contains polar groups such as carboxyl and amino groups, and forms hydrochloride salts, it may have good solubility in water, similar to some common organic salts, which can be ionized and soluble; in polar organic solvents such as methanol and ethanol, it also has a certain solubility. Due to the principle of similar miscibility, polar groups interact with polar solvents.
In terms of melting boiling point, in view of the existence of hydrogen bonds, van der Waals forces and other intermolecular forces in the structure, coupled with the large relative molecular mass, it is estimated that the melting point is higher, or between 200 ° C and 300 ° C, the melting point of many organic salts with complex structures is mostly in this range; boiling point or higher, but due to heat or decomposition, the exact boiling point is difficult to determine. The density of
has not yet been determined, but it is inferred from the structure containing benzene rings, heterocycles and many substituents that its density may be greater than that of water, due to the relatively dense groups such as benzene rings.

What is the use of this compound (3S- (2 (R * (R *)), 3R *)) -1,2,3,4-Tetrahydro-6,7-dimethoxy-2- (2- ((1- (ethoxycarbonyl) -3-phenylpropyl) amino) -1-oxopropyl) -3-isoquinolinecarboxylic acid monohydrochloride?

This compound is named (3S- (2 (R * (R *)), 3R *)) -1, 2, 3, 4-tetrahydro-6, 7-dimethoxy-2 - (2 - ((1 - (ethoxycarbonyl) -3 -phenylpropyl) amino) -1 -oxypropyl) -3 -isoquinoline carboxylic acid monohydrochloride. In ancient times, although there was no direct record of this specific compound, it was deduced from traditional pharmaceutical concepts, and may have unique functions in the field of medicine.

Looking at its structure, it contains a variety of groups. The isoquinoline carboxylic acid part may have the effect of regulating human qi and balancing yin and yang. In traditional medicine, many nitrogen-containing heterocyclic structural drugs often act on meridian qi and blood. This structure may achieve the purpose of promoting righteousness and removing evil by regulating the microscopic qi and blood circulation of the human body.

Ethoxycarbonyl and phenylpropyl and other parts may be related to the harmony of the viscera. The aromatic properties of phenyl, in traditional cognition, can enlighten the mind, or act on the mind and orifices, making the gods clear. The structure of ethoxycarbonyl may nourish and regulate the movement and transformation of the spleen and stomach and other viscera, helping the human body to stabilize the acquired nature.

However, these are all based on the analogy of ancient pharmaceutical concepts. There is no accurate record of the use of this compound by the ancients. And modern research on it requires rigorous scientific experiments, clinical trials, etc., in order to clarify its exact use and efficacy, and cannot be judged solely based on ancient concepts.

(3S- (2 (R * (R *)), 3R *)) -1,2,3,4-Tetrahydro-6,7-dimethoxy-2- (2- ((1- (ethoxycarbonyl) -3-phenylpropyl) amino) -1-oxopropyl) -3-isoquinolinecarboxylic monoacid hydrochloride What are the synthesis methods?

The synthesis of (3S - (2 (R * (R *)), 3 R *)) - 1,2,3,4 - tetrahydro - 6,7 - dimethoxy - 2 - (2 - ((1 - (ethoxycarbonyl) - 3 - phenylpropyl) amino) - 1 - oxypropyl) - 3 - isoquinoline carboxylic acid monohydrochloride is a key research direction in the field of organic synthesis. To obtain this compound, it is often synthesized by chemical method, and it requires multiple delicate reactions. < Br >
In the first step, a suitable starting material or a compound containing isoquinoline structure is often used as a group, and it is modified by a specific reaction to introduce functional groups such as methoxy groups. This process requires precise control of the reaction conditions, such as temperature, pH, and the ratio of reactants, etc., to ensure the smooth progress of the reaction.

In the second step, a side chain containing specific amino groups and ester groups is constructed. This may require the use of condensation reactions, substitution reactions, etc., to precisely connect the side chains to the isoquinoline parent. During this process, the selectivity and yield of the reaction are key considerations.

Furthermore, in the synthesis process, in order to ensure the correct configuration of the chiral center, or with the help of chiral catalysts, chiral additives and other delicate strategies to achieve specific stereochemical requirements.

Ultimately, the salt-forming reaction is also crucial. By moderately reacting with hydrochloric acid, the target monohydrochloride product is obtained. In this process, the reaction conditions need to be strictly controlled to avoid overreaction or side reactions in order to obtain a high-purity product.

After each step of the reaction, a variety of analytical methods, such as nuclear magnetic resonance, mass spectrometry, high performance liquid chromatography, etc., are required to confirm the structure and purity of the product, to ensure that the synthesis route is correct, and to approach the target compound step by step.

What is the price range of this (3S- (2 (R * (R *)), 3R *)) -1,2,3,4-Tetrahydro-6,7-dimethoxy-2- (2- ((1- (ethoxycarbonyl) -3-phenylpropyl) amino) -1-oxopropyl) -3-isoquinolinecarboxylic monoacid hydrochloride in the market?

This is (3S- (2 (R * (R *)), 3R *)) - 1,2,3,4 - tetrahydro - 6,7 - dimethoxy - 2 - (2 - ((1- (ethoxycarbonyl) -3 - phenylpropyl) amino) -1 - oxypropyl) -3 - isoquinoline carboxylic acid monohydrochloride, this compound is quite professional and special, on the market, its price range is difficult to determine. Due to many factors, the price will be influenced, such as the difficulty of the production process, if the preparation process is complicated, the required technology is exquisite, and the equipment requirements are strict, the cost will be high, and the price will also rise; the difficulty and cost of obtaining raw materials, if the raw materials are scarce, difficult to obtain or expensive, the price of the finished product will also be affected; market demand and supply conditions, if the demand is strong and the supply is limited, the price may rise, otherwise it may decrease; and product purity and Quality Standard, the price of products with high purity and strict Quality Standard is often higher. And this compound may be mostly used in specific scientific research fields or pharmaceutical research and development, and its transactions are mostly in professional channels, and the price information is difficult to be widely known to the public. Therefore, in order to know the exact price range, it is necessary to consult professional chemical product suppliers, scientific research reagent sales institutions, or explore relevant professional market platforms in order to obtain more accurate price information.