3-(Isopropoxycarbonyl-amino)-pyridine

3- (isopropoxycarbonyl-amino) pyridine is one of the organic compounds. Its chemical properties are quite elusive.
In this compound, the pyridine ring is aromatic, making its structure stable. The nitrogen atom on the pyridine ring has lone pairs of electrons, making it an electron donor to form coordination bonds with metal ions, etc., which may have applications in the fields of catalysis and materials science.
Isopropoxycarbonyl-amino moiety, containing carbonyl groups, has a certain polarity. Because the carbon-oxygen double bond electron cloud in the carbonyl group is biased towards the oxygen atom, the carbonyl carbon is partially positive and vulnerable to nucleophilic attack, and can participate in nucleophilic addition and other reactions. Amino can activate the pyridine ring, making it more prone to electrophilic substitution reactions, such as halogenation, nitration, etc. And amino can form salts with acids, or condensation reactions with aldides, ketones, etc.
isopropoxy adds specific physical properties to the molecule, such as affecting its solubility. Long-chain isopropoxy may reduce the solubility of compounds in water and increase their solubility in organic solvents.
3 - (isopropoxy carbonyl-amino) pyridine presents a variety of chemical properties due to the interaction of various parts of the structure. It may have potential application value in many fields such as organic synthesis, medicinal chemistry, etc. It can be used as an intermediate for the synthesis of more complex compounds.

3- (isopropoxycarbonyl-amino) pyridine has a wide range of common uses. In the field of medicinal chemistry, this compound is often a key intermediate for the creation of various biologically active drugs. Because its structure contains a pyridine ring and a specific amino substituent, it can interact specifically with targets in vivo, or it is a precursor structure for anticancer drugs. With its unique chemical properties, it interferes with the key pathway of cancer cell proliferation; or it is used to develop antibacterial drugs, hindering the physiological metabolism of bacteria, and achieving antibacterial effect.
In the field of materials science, it also has its uses. It can participate in the synthesis of functional polymer materials. Due to the rigidity of the pyridine ring and the reactivity of the amino group, the material has special electrical and optical properties. For example, polymers with fluorescent properties are prepared for chemical sensing, showing sensitive fluorescence responses to specific analytes to detect environmental pollutants or biomarkers.
In the field of organic synthesis, 3- (isopropoxycarbonyl-amino) pyridine is an important building block. Through various chemical reactions, such as nucleophilic substitution, coupling reactions, etc., complex organic molecular structures are constructed. Chemists use their unique activity check points to precisely construct target compounds, expand the boundaries of organic synthesis chemistry, and provide rich structural units for new drug research and development, new material creation, etc.

There are many ways to synthesize 3- (isopropoxycarbonyl-amino) pyridine. One method starts with 3-aminopyridine and interacts with isopropyl chloroformate under suitable reaction conditions. In an alkaline environment, the two can react with nucleophilic substitution. Bases such as triethylamine or potassium carbonate can help this reaction and promote the reaction to form the target product. When reacting, it is necessary to pay attention to the control of temperature and reaction time. Generally speaking, the temperature should be maintained at low temperature to room temperature. After several hours of reaction, the corresponding product can be obtained, and then the separation and purification techniques, such as column chromatography, can be obtained. Pure 3- (isopropoxycarbonyl-amino) pyridine.
There is another method, which can first use pyridine as the starting material, through a specific reaction step, introduce the amino group at the 3-position of the pyridine ring, and then react with the amino group and isopropyl chloroformate to form the target compound. In this process, the step of introducing amino groups may require multiple steps of reaction, and the control of the reaction conditions of each step is also crucial. For example, it may be necessary to take advantage of the activity of pyridine, through a series of reactions such as halogenation and nucleophilic substitution, first introduce a suitable substituent, then convert it into an amino group, and then react with isopropyl chloroformate. After the reaction is completed, it also needs to be carefully separated and purified to obtain a high-purity product.
Furthermore, there are also methods for synthesis by condensation and other reactions with the help of other nitrogen-containing reagents and suitable ester compounds. These reactions may involve more complex reaction mechanisms and conditions, but they all achieve the combination of 3- (isopropoxycarbonyl-amino) pyridine. Each method has its advantages and disadvantages, and the synthesizer should carefully choose the appropriate method according to the actual demand, the availability of raw materials, and the difficulty of reaction.

I do not know the price range of 3- (isopropoxycarbonyl-amino) pyridine in the market. The price of this compound often varies due to many factors, such as the quality, the amount purchased, and the different suppliers, and the market price is also in dynamic changes.
If you want to know the exact price, you may need to study the chemical raw material trading market in detail, consult chemical product suppliers, or refer to professional chemical product price information platforms. In the genus of "Tiangong Kaiwu", there were no such fine chemical compounds at that time, so it was difficult to ask the price according to it. Today's chemical industry is complex and the price is not constant. It is necessary to study the real-time market conditions carefully to obtain its approximate price range.

3 - (isopropoxycarbonyl-amino) pyridine is a chemical substance. Its storage is essential to its physical and chemical properties. It must be carried out in accordance with scientific methods to ensure its stability and safety.
This substance is sensitive to temperature and humidity. If the temperature is high, the molecule will be dramatic, or cause structural change or sexual change; if it is wet, it is easy to deliquescence, and it will react with water, and it will be bad. Therefore, it should be stored in a cool and dry place. The temperature is preferably 15-25 degrees Celsius, and the humidity is controlled at 40% -60%.
and protected from light. Light has energy, or induces photochemical reaction, causing decomposition or allosterization. When placed in a dark room, or stored in an opaque device. And it or with other substances should not be mixed with strong oxygen agents, acids, and alkalis. Strong oxygen agents cause oxidation, and acids and bases cause acid and alkali to cause damage to their quality. It must be placed separately, and the category, sex and precautions should be carefully marked.
The packaging is also heavy. Choose the appropriate device, seal it tightly, and prevent leakage and gas entry. Glass or plastic bottles and jars can be used. Natural plastic may swell a certain chemical product, so choose carefully when using it.
Daily inspection should not be ignored. Regularly observe its state, color and taste. If there is any difference, quickly check the cause to ensure the safety and quality of the storage.