Chemical Formula | C16H21NO4 |
Molecular Weight | 291.34 |
Appearance | Solid (usually white or off - white) |
Physical State At Room Temperature | Solid |
Melting Point | Specific value would require experimental determination |
Solubility In Water | Low solubility in water |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Chirality | Chiral, has D - configuration |
Functional Groups | BOC (tert - butyloxycarbonyl), carboxylic acid, tetrahydroisoquinoline ring |
Pka Carboxylic Acid | Typical carboxylic acid pKa range around 4 - 5 |
Stability | Stable under normal conditions but sensitive to strong acids (can cleave BOC group), strong bases |
What is the chemical structure of N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
Alas! This N-1-BOC-D-1,2,3,4-tetraquinoline-3-carboxylic acid is one of the most important compounds. Its chemical properties are excellent.
First of all, the BOC is tert-butoxycarbonyl, which is often used as the support group of the amino group. In this compound, the BOC is placed on the nitrogen atom to maintain the activity of the nitrogen atom, so that it can be used in the reaction of the multiplication, so as not to be unnecessary. If it is not important,
Furthermore, D-1,2,3,4-tetraquinoline, this is a thick framework. Quinoline, which contains nitrogen, is aromatic and tetrachemical, and its degree of harmony increases, and its properties are also affected by quinoline. In this framework, the nitrogen atom and the carbon atom are co-determined, and the addition of four atoms gives it specific chemical properties, and affects its physical and chemical activities.
For 3-carboxylic acids, there is a carboxyl group at the third position of tetraquinoline. The carboxyl group is functional and acidic. It can react to polyacids, esterification reactions, etc. The existence of this carboxyl group greatly changes the chemical properties of this compound, making it possible to react to many compounds such as alcohols and amines, and to create more derivatives.
Therefore, N-1-BOC-D-1,2,3,4-tetraquinoline-3-carboxylic acid is composed of nitrogen, tetraquinoline-3-carboxylic acid of BOC, and the carboxyl group of the 3-position is formed together, and the parts are influenced by each other, so that it has unique chemical properties. It is used in the fields of synthesis, physicochemistry, etc., or has important uses.
What are the main uses of N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is a crucial compound in the field of organic synthesis. It has a wide range of uses, first in the field of medicinal chemistry. The construction of many drug molecules often relies on this compound as a key intermediate. Due to its unique structure, it can be modified by various chemical reactions, and then derived new compounds with different pharmacological activities.
In the field of alkaloid synthesis, this compound also plays a pivotal role. Alkaloids are natural products, many of which have complex chemical structures and significant biological activities. N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid can be used as a starting material or key fragment to help achieve the total synthesis of alkaloids, laying the foundation for the study of the biological activity and mechanism of action of alkaloids.
Furthermore, in the field of materials science, based on this compound, through specific reactions, functional materials with unique properties can be prepared. For example, it can participate in polymerization reactions to construct polymer materials with special optical and electrical properties, opening up new directions for the development of materials science.
In conclusion, N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids play an indispensable role in many fields such as medicinal chemistry, alkaloid synthesis and materials science, and promote the continuous progress and development of related fields.
What is the synthesis method of N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
To prepare N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, the method is as follows:
First take D-1,2,3,4-tetrahydroisoquinoline as the starting material, use Boc O2 O as the protective base reagent, and add an organic base, such as triethylamine, to a suitable solvent, such as dichloromethane, for temperature control reaction. This step aims to protect the nitrogen atom by BOC, because the BOC protective group can increase the stability of the substrate and is easy to remove in subsequent reactions. The reaction mechanism is that Boc -2 O is catalyzed by a base, and nucleophilic substitution occurs, and the BOC group is attached to the nitrogen atom. < Br > times, the protected product is oxidized under specific conditions by a suitable oxidant, such as potassium permanganate or potassium dichromate, to convert the side chain into a carboxyl group. This oxidation reaction requires fine adjustment of the reaction conditions, such as temperature, pH value, etc., to preserve the selectivity and yield of carboxylic acid products.
After the reaction is completed, the product is purified by conventional separation methods, such as extraction, column chromatography, etc. During extraction, an appropriate organic solvent is selected to enrich the product in the organic phase. After column chromatography, according to the polarity difference between the product and the impurity, pure N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is obtained. Each step of the reaction requires fine monitoring to ensure product quality and yield, and the conditions of each step are fine-tuned and optimized according to the actual situation.
What are the physical and chemical properties of N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is an organic compound with unique physical and chemical properties. Its appearance may be white to off-white solid, due to the orderly arrangement of molecular structures and the characteristics of light reflection. In terms of melting and boiling point, the melting point is about [X] ° C, and the boiling point is about [X] ° C. It is determined by intermolecular forces and structural stability. Intermolecular hydrogen bonds and van der Waals forces jointly maintain a specific temperature state.
In terms of solubility, the compound is slightly soluble in water. Due to the large proportion of hydrophobic groups in the molecule, water interacts weakly with it; but it is soluble in common organic solvents such as dichloromethane, chloroform, etc., and the organic solvent and the intermolecular force are conducive to dissolution.
In terms of stability, it is relatively stable under conventional conditions. When encountering strong acids, strong bases or high temperatures, some structures such as BOC protecting groups and carboxyl groups may change. For example, in strong acids, the BOC protecting group is easy to remove, and it is broken due to the combination of protons and oxygen atoms in the BOC group; in strong bases, the carboxyl group or salt forms, which changes its chemical properties.
In addition, it is widely used in the field of organic synthesis. It uses carboxyl groups to react with amino groups, hydroxyl groups, and other groups to build complex compounds, providing important intermediates for drug research and development, materials science, etc., and achieving specific functions with unique structural properties.
What is the price range of N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid in the market?
I haven't heard of the exact price range of "N-1-BOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid" on the market. This compound is not commonly available, and its price varies due to many factors.
First, purity is crucial. For high purity, it is difficult to prepare, and it requires delicate processes and complicated steps. Its price is high; for low purity, it is easier to prepare, and the price is slightly lower. If the purity is above 99%, the price must far exceed that of 95% purity.
Second, the preparation scale also affects. In large-scale production, due to the scale effect, the unit cost may decrease, and the price may also decrease; small-scale preparation, the cost is high, and the price is also high.
Third, market supply and demand determine the price. If there are many people who want it, but there are few people who supply it, the price must rise; if there is less market demand and more supply, the price may decrease.
Fourth, the cost of raw materials is also the key. Raw materials are scarce or difficult to prepare, the cost is high, and the price of finished products is also high.
And this compound may require special storage and transportation conditions, such as low temperature, drying, etc., which will also increase the cost and affect the price. Therefore, in order to know the exact price range, it is necessary to consult the relevant chemical raw material suppliers in detail, depending on the specific quality, quantity and other factors, in order to obtain an accurate quotation.