Benzyl 4-hydroxytetrahydro-1(2H)-pyridinecarboxylate

Benzyl 4-hydroxytetrahydro-1 (2H) -pyridinecarboxylate, this is a kind of organic compound. To understand its chemical structure, it is necessary to analyze the meaning of each part in its name.
"Benzyl" is benzyl, which is a common organic group, represented by -CH ² C H. It is derived from benzene, a hydrogen atom on the benzene ring is replaced by methyl, and has aromatic properties.
"4-hydroxy", showing that the hydroxy group (-OH) is attached to the 4th position of the pyridine ring. Hydroxyl groups are active functional groups and can participate in many chemical reactions, such as esterification, etherification, etc., which have a great influence on the physical and chemical properties of compounds and often increase their hydrophilicity.
"Tetrahydro-1 (2H) -pyridine" refers to the part of the pyridine ring. Pyridine is a nitrogen-containing six-membered heterocycle and has aromatic properties. "Tetrahydro" means that four carbon-carbon double bonds on the epipyridine ring are hydrogenated and reduced to a saturated or partially saturated state. A double bond is formed between the 1st and 2nd positions adjacent to the nitrogen atom of the 1 (2H) epipyridine ring, and the hydrogen at the 2nd position can participate in the reaction under specific conditions.
"Formate", that is, -COO-group, indicates that this compound contains an ester bond. This ester bond is connected at one end to a pyridine ring and at the other end to a benzyl group.
In summary, the chemical structure of benzyl 4-hydroxytetrahydro-1 (2H) -pyridinecarboxylate is: a partially hydrogenated pyridine ring as the core, a hydroxyl group at the 4th position, and a benzyl group at the 1st position on the ring through an ester bond. This structure makes the compound have both aromatic, hydroxyl activity and ester properties, and may have potential uses in the fields of organic synthesis and medicinal chemistry. It can be used as an intermediate to prepare more complex organic compounds.

Benzyl 4-hydroxytetrahydro-1 (2H) -pyridinecarboxylate is an organic compound with important uses in many fields.
In the field of pharmaceutical chemistry, it can be used as a key intermediate for drug synthesis. The construction of many drug molecules often requires the use of such compounds containing specific functional groups as starting materials or key building blocks. By performing a series of chemical modifications and reactions on benzyl 4-hydroxytetrahydro-1 (2H) -pyridinecarboxylate, such as substitution reactions and addition reactions, the molecular structure of drugs with specific biological activities can be precisely constructed, and then new drugs for the treatment of various diseases can be developed.
In the field of organic synthetic chemistry, it is also an extremely important synthesizer. Due to the functional groups such as pyridine ring, hydroxyl group and benzyl ester group contained in its structure, it can participate in a variety of classical organic reactions, such as nucleophilic substitution, electrophilic substitution, and oxidation-reduction reaction. With these reactions, chemists can convert it into more complex and diverse organic compounds, enrich the variety of organic compounds, and provide a key material basis for the development of organic synthetic chemistry.
In the field of materials science, it may also show potential application value. Through appropriate modification and polymerization, it may be possible to prepare polymer materials with special properties, such as materials with specific optical, electrical or mechanical properties, which can be applied to many aspects such as optoelectronic materials, high-performance polymers, etc.
In summary, benzyl 4-hydroxytetrahydro-1 (2H) -pyridyl carboxylate plays an indispensable role in the fields of medicine, organic synthesis and materials, and is of great significance to promote scientific research and technological development in related fields.

The synthesis of benzyl 4-hydroxytetrahydro-1 (2H) -pyridyl carboxylic acid esters has various approaches. One can be started from a suitable pyridine derivative and hydrogenated to obtain a tetrahydropyridine structure. For example, taking a pyridine with the corresponding substituent, in the presence of a suitable catalyst such as palladium carbon, using hydrogen as a hydrogen source, under appropriate temperature and pressure conditions, catalytic hydrogenation can reduce the double bonds of the pyridine ring to obtain a tetrahydropyridine parent nucleus.
Then, a hydroxyl group is introduced at the 4-position of the tetrahydropyridine. This step can be achieved by a nucleophilic substitution reaction. If the 4-position of tetrahydropyridine is connected with a suitable leaving group, such as a halogen atom, it is attacked by a nucleophilic reagent hydroxyl anion (which can be formed from a base and water). Hydroxyl groups can be introduced through a substitution reaction.
As for the introduction of benzyl groups, esterification can be used. With tetrahydropyridine derivatives containing carboxyl groups and benzyl alcohol, under acid catalysis, such as concentrated sulfuric acid or p-toluenesulfonic acid, under heating conditions, an esterification reaction occurs to generate benzyl 4-hydroxytetrahydro-1 (2H) -pyridine carboxylate. < Br >
Or benzyl alcohol is first prepared into benzyl halide, and then reacts with carboxyl-containing tetrahydropyridine derivatives under alkali action to form the target product through nucleophilic substitution. These synthesis methods have their own advantages and disadvantages, and need to be carefully selected according to factors such as the availability of raw materials, the difficulty of reaction conditions and the purity requirements of the product.

Benzyl 4-hydroxytetrahydro-1 (2H) -pyridinecarboxylate, an organic compound. Its physicochemical properties are crucial, and it is related to its performance in various chemical processes and practical applications.
First talk about physical properties. Under normal circumstances, it may be in a solid state, but the exact physical form is also affected by surrounding environmental factors, such as temperature and pressure. Its melting point and boiling point are important characteristics. The melting point reveals the temperature required to change from solid to liquid, and the boiling point indicates the temperature from liquid to gas. Unfortunately, I do not have a specific value. This may be due to the precise physical constants of the compounds often determined by high-standard experiments, and different experimental conditions may cause slight differences.
When it comes to chemical properties, in the molecular structure, benzyl and 4-hydroxytetrahydro-1 (2H) -pyridine carboxylic acid ester moiety endow it with various reactivity. Hydroxyl groups are nucleophilic and can participate in many reactions, such as esterification reaction, which can react with carboxylic acid compounds under suitable conditions to form corresponding esters. This process may require catalysts and specific temperature and time conditions. The pyridine ring part also affects the distribution of molecular electron clouds, making it easy to participate in electrophilic substitution reactions, introducing other functional groups at specific positions in the pyridine ring, thereby expanding the use of compounds. The phenyl ring in benzyl has not only the conjugation stability of benzene, but also changes the electronic effect of the whole molecule due to its connection with ester groups, which affects its chemical activity and reaction selectivity.
In conclusion, although detailed physical and chemical properties of benzyl 4-hydroxytetrahydro-1 (2H) -pyridyl carboxylate have not been obtained, it can be seen from its molecular structure analysis that it may have rich reaction possibilities in the field of organic synthesis. In many disciplines such as medicinal chemistry and materials science, or because of its unique physical and chemical properties, it shows important value, laying the foundation for further research and application.

I look at the "Benzyl 4 - hydroxytetrahydro - 1 (2H) -pyridinecarboxylate" you are inquiring about, which is the English name of the chemical substance. However, it is not easy to know its price range in the market.
Because the market price is often affected by many factors. First, the difficulty of obtaining raw materials and the price. If the raw materials for making this substance are scarce or expensive, the price of the finished product will also rise. Second, the complexity of the production process, the complexity of the process requires more manpower, material resources and time investment, which will affect the price. Third, the market supply and demand situation, if the demand is strong and the supply is limited, the price will be high; conversely, if the supply exceeds the demand, the price will be low. < Br >
And the price of this substance may vary widely in different markets and suppliers. In the professional chemical reagent market, due to the specific needs of scientific research and production, the quality control is strict, and the price may be relatively stable and high. In the large market of chemical raw materials, if the output is considerable, the price may be more flexible due to factors such as competition.
It is difficult for me to obtain the exact price range. If you want to know the details, you can consult a professional chemical reagent supplier, or explore it on the chemical product trading platform, so that you can get more accurate price information to meet your needs.