2-(Methylamino)-3-pyridinemethanol

2-%28Methylamino%29-3-pyridinemethanol is 2 - (methylamino) -3 -pyridine methanol, and its chemical structure can be summarized as follows.
This compound belongs to a pyridine derivative, and the pyridine ring is its core structure. The pyridine ring is formed by connecting five carbon atoms and one nitrogen atom in a six-membered cyclic conjugate system, which is aromatic. In the second position of the pyridine ring, there is a methylamino group (-NHCH). In this methylamino group, the nitrogen atom is covalently bonded to the carbon atom at the second position of the pyridine ring, and the nitrogen atom is connected to a methyl group (-CH 🥰), which is bound to the nitrogen atom through a carbon-nitrogen bond. At the 3rd position of the pyridine ring, a methanol group (-CH 2O OH) is connected, that is, after a methylene (-CH 2O -) is connected to a hydroxyl group (-OH), the methylene is connected to the 3rd position of the pyridine ring by a carbon-carbon bond.
Overall, the chemical structure of 2 - (methylamino) -3 - pyridine methanol is combined by different atoms and groups in a specific way, and the parts interact with each other, giving the compound unique physical and chemical properties. It may have important uses in organic synthesis, medicinal chemistry and other fields.

2-%28Methylamino%29-3-pyridinemethanol, Chinese name 2 - (methylamino) -3 -pyridyl methanol. This is an organic compound with specific physical properties.
Looking at its properties, it is mostly white to light yellow crystalline powder at room temperature and pressure. The texture is fine, like fine jade chips. This is due to its regular and orderly molecular arrangement and moderate interaction force, resulting in its solid state appearance.
The melting point is about 110-114 ° C. When the temperature gradually rises, the molecular thermal motion intensifies enough to overcome the lattice energy, and then gradually melts from the solid state to the liquid state, just like ice and snow melt when warm. The characteristics of the melting point are the key indicators for the purity and structural stability of this compound.
In terms of solubility, it is soluble in many organic solvents, such as methanol, ethanol, dichloromethane, etc. In methanol, it dissolves quickly like a salt in water. Due to the formation of hydrogen bonds or van der Waals forces between the molecules, it interacts with the solvent molecules and thus dissolves each other. However, in water, the solubility is limited, due to the poor matching of molecular polarity with water molecules, it can only be slightly soluble, such as sand and gravel in flood flow, only slightly dispersed.
In addition, 2 - (methylamino) -3 -pyridine methanol has a certain hygroscopicity. In a high humidity environment, it absorbs water like a dry sponge, which will absorb moisture in the air and cause its own deliquescence. Therefore, it should be stored in a dry place to prevent changes in its properties and affect its quality and application.

2-%28Methylamino%29-3-pyridinemethanol, that is, 2 - (methylamino) -3 -pyridyl methanol, this substance has a wide range of uses.
In the field of medicinal chemistry, it is often a key intermediate. Due to the coexistence of pyridine and methanol structures and the presence of methylamino groups, it is endowed with unique chemical activity and spatial structure. With this property, chemists can modify its structure through various organic reactions to synthesize a series of compounds with specific biological activities. Some compounds may have antibacterial effects, can inhibit bacterial growth and reproduction, and can be used to develop new antibacterial drugs, providing the possibility of fighting bacterial infections and diseases; or have the potential to regulate the function of the nervous system, laying the foundation for the treatment of neurodegenerative diseases, psychiatric diseases and other drug development.
In the field of materials science, 2 - (methylamino) -3 -pyridyl methanol can also be used. Due to its special structure, it may participate in the synthesis process of specific materials. For example, when preparing some functional polymer materials, it can be introduced into the polymer chain as a functional monomer to give the material special properties. Or improve the solubility and processability of the material, making the material easier to form and process; or give the material the ability to recognize and adsorb specific substances, used in the preparation of separation membranes, sensors and other materials to achieve efficient separation and sensitive detection of specific substances.
Furthermore, in the field of organic synthetic chemistry, it is often used as an important building block for organic synthesis. The different functional groups in its molecules can be spliced and combined with other organic compounds through classical organic reactions, such as substitution reactions, addition reactions, etc. Chemists can use these reactions to construct complex and diverse organic molecules, providing rich raw materials and pathways for the development of organic synthetic chemistry, and helping to synthesize more organic compounds with potential application value.

There are various methods for the synthesis of Fu 2 - (methylamino) -3 -pyridine methanol in the past. One is to use pyridine derivatives as the starting material and go through a multi-step reaction to form it. First, a suitable pyridine compound is taken, and under specific reaction conditions, a specific position on the pyridine ring is substituted to introduce a group containing methyl amino groups. This step requires careful selection of the reaction reagents and reaction conditions to ensure that the reaction proceeds in the expected direction and has a high yield.
Furthermore, another position on the pyridine ring is modified to introduce hydroxymethyl groups. This process may involve many reaction steps such as nucleophilic substitution and redox. Each step requires fine regulation, such as reaction temperature, reaction time, and the proportion of reactants. A slight difference may affect the purity and yield of the product.
Another method of synthesis is to start from more basic raw materials, gradually build a pyridine ring, and then introduce methyl amino and hydroxymethyl groups. Although this approach is relatively common and easy to obtain starting materials, the process of building a pyridine ring is complicated, and it requires deep knowledge of organic synthesis chemistry. The harsh reaction conditions and cumbersome reaction steps all require extremely high skill and patience of the synthesizer.
In the synthesis process, separation and purification are also key. The product is often mixed with unreacted raw materials, by-products and other impurities. Appropriate separation techniques, such as column chromatography and recrystallization, are required to obtain high-purity 2- (methylamino) -3-pyridyl methanol. These synthesis methods rely on the wisdom and experience of organic synthesis chemists, and can only be used after repeated trials and optimization.

2-%28Methylamino%29-3-pyridinemethanol is 2 - (methylamino) -3 -pyridyl methanol. When storing and transporting this substance, many matters need to be carefully paid attention to.
Store first, and choose the first environment. It must be placed in a cool, dry and well-ventilated place. It is easy to cause qualitative changes due to humidity and warmth. For example, if it is placed in a damp place, it may cause deliquescence, which will damage its purity and quality. Furthermore, it is necessary to keep away from fires and heat sources. This is because it has certain chemical activity. In case of open flames and hot topics, it is dangerous, such as burning or even exploding. At the same time, it should be stored separately from oxidants and acids. Contact with them or react violently, endangering safety. The storage place should also be equipped with suitable materials to contain leaks in case of leakage and can be properly handled in a timely manner.
As for transportation, the packaging must be tight and sturdy. Make sure that it will not be damaged and leaked during bumpy handling. During transportation, it is also necessary to avoid high temperatures and open flames, and the traffic is smooth, and there should be no excessive vibration or impact. Transportation vehicles should also be equipped with corresponding fire fighting equipment and leakage emergency treatment equipment to prepare for emergencies. Escort personnel must be professionally trained, familiar with the characteristics of this object and emergency treatment methods, and strictly guarded during transportation. In this way, the safety of 2- (methylamino) -3-pyridyl methanol during storage and transportation is guaranteed.