(S)-N-Tert-Butyl-1,2,3,4-Tetrahydroisoquinoline-3-Carboxamide

(S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide, this is an organic compound. Looking at its name, it is composed of several parts.
" (S) " indicates its stereochemical configuration, which is a specific configuration identification for chiral compounds, indicating that the molecule has a chiral center and is determined to be this configuration according to specific rules.
"N-tert-butyl", "N" refers to the nitrogen atom, indicating that the tert-butyl is attached to the nitrogen atom. Tert-butyl is an alkyl group with a specific structure, with the structure of -C (CH <
"1,2,3,4-tetrahydroisoquinoline". This is the parent nuclear structure. After the hydrogenation of isoquinoline, the double bonds of positions 1, 2, 3, and 4 are hydrogenated to form a tetrahydroisoquinoline ring system. This ring has a certain rigidity and conjugate structure, which affects the electron cloud distribution and reactivity of the compound.
"-3-formamide" means that there is a formamide group attached to the 3 position of the tetrahydroisoquinoline ring. Formamido-CONH ² has certain polarity and reactivity, and can participate in a variety of chemical reactions, such as hydrogen bond formation, nucleophilic substitution, etc.
In summary, the chemical structure of (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide gives it unique physical and chemical properties and potential biological activities due to the interaction of various parts, which may have important research value in the fields of organic synthesis and medicinal chemistry.

(S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide is widely used in the field of medicine and chemical industry.
First, it is often used as a key intermediate in the process of drug development. Many bioactive compounds rely on it to build a specific molecular structure during synthesis. Because of the structure of 1,2,3,4-tetrahydroisoquinoline, it is common in many bioactive molecules, and the modification of formamide and tert-butyl can endow the compounds with unique physical, chemical and biological properties. For example, some drugs with potential anti-tumor activity, with (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide, can precisely regulate the interaction between molecules and targets, enhance the affinity between drugs and receptors, and then improve drug efficacy.
Second, in the art of organic synthesis, it is an important building block. Chemists can use it as a starting material to construct complex and novel organic molecules through various chemical reactions, such as nucleophilic substitution, redox, etc. Due to the existence of chiral centers, it can be used to prepare optically active compounds, which is of great significance in the field of asymmetric synthesis. It can assist in the synthesis of products with a single chiral configuration, and such products often have unique properties in medicine, pesticides and materials science.
Third, in the field of materials science, or through specific modifications and polymerization reactions, it is introduced into polymer materials. Give the material special optical, electrical or mechanical properties. For example, when preparing polymer materials with fluorescent properties, (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide structural units may improve the luminous efficiency and stability of the material, opening up new possibilities for material applications.

To prepare (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide, the method is as follows:
First take the appropriate starting material, such as a compound containing isoquinoline structure as the base. It can be modified by specific reaction conditions. Usually by means of chemical synthesis, following the principle of organic synthesis, select the appropriate reagents and reaction steps.
The first step, or the specific position of the starting material, with the appropriate nucleophilic reagent or electrophilic reagent, initiates the reaction to introduce the necessary functional groups. This step requires precise control of the reaction conditions, such as temperature, pH and reaction time, to ensure that the reaction proceeds in the desired direction. < Br >
Second, convert and modify the introduced functional group. For example, with suitable oxidation or reduction reagents, adjust the oxidation state of the functional group to meet the structural requirements of the target product. In the meantime, separation and purification techniques are also indispensable to remove impurities and maintain the purity of the reaction product.
Or use the method of chiral induction to introduce chiral centers to obtain products with (S) configuration. Chiral catalysts or chiral adjuvants can be used to induce the formation of chiral in the reaction. This step is extremely sensitive to factors such as temperature and catalyst dosage, and must be carefully regulated.
Furthermore, for the obtained intermediate product, according to the structure of the target product, condensation or substitution reactions are carried out, and tert-butyl and formamido are added. In this step, suitable reaction solvents and alkali or acid catalysts need to be selected to promote the smooth occurrence of the reaction.
After each step of the reaction, various analytical methods, such as thin-layer chromatography, nuclear magnetic resonance, etc., are used to test the structure and purity of the product. If there is anything unexpected, the reaction conditions need to be adjusted or the reaction steps need to be changed. After careful design and operation of multiple steps, (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide can finally be obtained.

(S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide is one of the organic compounds. Its physical properties are unique and are of great significance in chemical research and related fields.
Looking at its properties, under normal temperature and pressure, it mostly shows a white to quasi-white solid state, which is conducive to storage and operation. The value of its melting point is crucial for the identification and purification of this compound. It has been experimentally determined that the melting point of (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide is within a certain range, but the specific value may fluctuate slightly due to slight differences in experimental conditions.
In terms of solubility, the performance of this compound in organic solvents is particularly important. In common organic solvents, it has a certain solubility in some organic solvents, such as dichloromethane, chloroform, etc. This property provides convenience for the separation, purification and choice of reaction medium in organic synthesis. However, in water, its solubility is not good, and the lid has a large proportion of hydrophobic groups in its molecular structure, resulting in weak interaction with water molecules.
In addition, the density of (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide is also a key part of its physical properties. Although the exact density value needs to be determined by professional instruments under specific conditions, knowing the approximate range is helpful to consider its location and mixing characteristics in the solution system.
In terms of stability, under normal conditions, if there is no specific chemical reaction conditions to trigger, this compound is relatively stable. In case of high temperature, strong acid-base or specific catalyst, or a chemical reaction occurs, the structure changes, and the physical properties also change.
From the above, it can be seen that the physical properties of (S) -N-tert-butyl-1,2,3,4-tetrahydroisoquinoline-3-formamide, such as properties, melting point, solubility, density and stability, are interrelated, which together affect its application and research in the field of chemistry.

I look at the " (S) -N-Tert-Butyl-1,2,3, 4-Tetrahydroisoquinoline-3-Carboxamide" you are inquiring about. This is a fine chemical substance. However, its market price is difficult to determine. The change in its price depends on many factors.
The first one to bear the brunt is the difficulty of preparation. If the preparation method is cumbersome, requires rare raw materials, goes through multiple complicated processes, and the yield is not high, its price will be high. On the contrary, if the preparation method is simple and the raw materials are easy to obtain, the price may be close to the people.
Second, the state of market supply and demand is also the key. If there is strong demand for this product in the fields of medicine, chemical industry, etc., but the supply is limited, its price will rise; if there is little demand and the supply is full, the price will decline.
Furthermore, different manufacturers can also cause price differences. Large factories may be able to produce at a relatively low cost due to their economies of scale and excellent craftsmanship; small factories may be priced differently due to higher costs.
And market prices are not static. Over time, the rise and fall of raw material prices, technological innovation, and policy adjustments can all make their prices fluctuate. Therefore, if you want to know the exact market price of this product, you should consult chemical raw material suppliers, relevant trade platforms, or conduct detailed research in the market to obtain a more accurate figure. It is difficult to determine the price based on empty words alone.