2 Amino 5 Iodo 3 Picoline
Iodobenzene

2 Amino 5 Iodo 3 Picoline

Fengxi Chemical

Specifications

HS Code

966126

Chemical Formula C6H7IN2
Molecular Weight 236.037
Appearance Solid (likely powder or crystalline)
Color Typically white to off - white
Odor May have a faint organic odor
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Melting Point Data - specific value (needs further research)
Boiling Point Data - specific value (needs further research)
Pka Value Data - specific value (needs further research)
Stability Stable under normal conditions, but may react with strong oxidizing agents
Hazardous Nature May be harmful if swallowed, inhaled or in contact with skin
Name 2-amino-5-iodo-3-picoline
Chemical Formula C6H7IN2
Molar Mass 236.038 g/mol
Appearance Solid (usually a powder)
Color Off - white to light yellow
Solubility In Water Slightly soluble
Melting Point 108 - 112 °C
Flash Point N/A (solid, flash point concept more relevant for flammable liquids)
Pka N/A (no readily available pKa data for this compound in common literature)
Chemical Formula C6H7IN2
Molecular Weight 236.037
Appearance Solid (Typical)
Solubility In Water Poorly soluble (Typical for this class)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, chloroform
Vapor Pressure Low (Expected for a solid)
Stability Stable under normal conditions, avoid strong oxidizing agents
Chemical Formula C6H7IN2
Molecular Weight 236.04
Appearance Solid (usually)
Color May be off - white to light - colored solid
Odor Typically has a characteristic organic odor
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in some common organic solvents like dichloromethane, chloroform
Melting Point Specific value depends on purity, typically in a certain range of melting temperatures
Boiling Point Higher boiling point due to its structure
Pka Value Related to the basicity of the amino group, has a characteristic pKa
Packing & Storage
Packing 250g of 2 - amino - 5 - iodo - 3 - picoline packaged in a sealed, chemical - resistant bottle.
Storage 2 - amino - 5 - iodo - 3 - picoline should be stored in a cool, dry, well - ventilated area. Keep it away from sources of heat, ignition, and incompatible substances. Store in a tightly closed container to prevent moisture absorption and exposure to air. Avoid storing near strong oxidizing agents or acids to prevent potential chemical reactions.
Shipping 2 - amino - 5 - iodo - 3 - picoline is shipped in sealed, corrosion - resistant containers. It adheres to strict chemical shipping regulations, ensuring proper handling to prevent spills and maintain safety during transit.
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2-amino-5-iodo-3-picoline 2-amino-5-iodo-3-picoline 2-amino-5-iodo-3-picoline
General Information
Frequently Asked Questions
What is the chemical structure of 2-amino-5-iodo-3-picoline?
The chemical structure of 2-amino-5-iodo-3-picoline is as follows:
The pyridine ring is a six-membered nitrogen-containing heterocyclic ring, and the nitrogen atom occupies a position on the ring. The second position of the pyridine ring is connected to the amino group ($- NH_ {2} $), the third position is connected to the methyl group ($- CH_ {3} $), and the fifth position is connected to the iodine atom ($-I $). This compound combines the aromatic properties of the pyridine ring and the characteristics of amino, methyl and iodine atoms. The pyridine ring is composed of five carbon atoms and one nitrogen atom in a sp ² hybrid orbital to form a sigma bond, and a closed conjugated large π bond is formed by overlapping the side of the p orbital, which endows it with certain stability and special electron cloud distribution. The amino group has certain basic and nucleophilic properties, and the methyl group is the power supply group, which will affect the electron cloud density of the pyridine ring, while the iodine atom can participate in various reactions such as nucleophilic substitution. This structure determines the potential application value of 2-amino-5-iodine-3-methyl pyridine in organic synthesis, pharmaceutical chemistry and other fields.
What are the main uses of 2-amino-5-iodo-3-picoline?
2-Amino-5-iodo-3-picoline is 2-amino-5-iodine-3-methylpyridine. This substance has a wide range of uses and is often used as a key intermediate in the synthesis of medicine. Due to its unique chemical structure, it can participate in various chemical reactions and help create various pharmaceutical active ingredients.
In the field of materials science, it has also made a name for itself. It can be used to develop new functional materials, such as materials with special photoelectric properties. Due to the structure of amino groups, iodine atoms and methylpyridine in the molecule, it endows it with unique electronic properties, which can affect the conductivity, optical absorption and emission properties of materials.
In the field of pesticide synthesis, it also has a place. It can be used as a raw material to synthesize pesticides with high insecticidal, bactericidal or herbicidal activities. With its chemical activity, it can precisely act on target organisms to achieve the purpose of pest control and weed control.
In the field of organic synthetic chemistry, 2-amino-5-iodine-3-methylpyridine, as an important building block, can construct complex organic molecular structures through coupling reactions, substitution reactions, etc., providing an effective way for the synthesis of novel organic compounds and promoting the development of organic synthetic chemistry.
What are 2-amino-5-iodo-3-picoline synthesis methods?
The synthesis method of 2-amino-5-iodine-3-methylpyridine is a very important topic in the field of organic synthesis. The synthesis route can be achieved by different chemical reaction steps starting from a variety of starting materials.
One method can first take an appropriate pyridine derivative as the starting material. If 3-methylpyridine is used as the starting point, it should be iodized with an iodine source under specific conditions. For this iodization step, a suitable reaction reagent and reaction environment need to be selected. The common iodine source may be iodine elemental substance ($I_2 $), accompanied by an appropriate catalyst, such as a copper salt catalyst. In a specific solvent system, such as a polar organic solvent, heating or light is applied to promote iodization of the 5-position of the pyridine ring to obtain 5-iodine-3-methylpyridine.
Then, the 5-iodine-3-methylpyridine is reacted with an amination reagent. In the amination step, ammonia or ammonia derivatives can be selected. If ammonia is used, it is often necessary to replace the hydrogen atom at the 2-position of the pyridine ring with an amino group at high temperature and pressure, and in the presence of a suitable catalyst, to obtain 2-amino-5-iodine-3-methylpyridine.
Another way is to modify the pyridine ring by amination first, and then carry out the iodization reaction. First, the 2-position of 3-methylpyridine is aminated with a suitable aminylating agent. This aminylating agent, or an active compound containing an amino group, introduces the amino group into the 2-position of the pyridine ring under specific reaction conditions. After that, the 2-amino-3-methylpyridine is iodized, and the iodine atom is introduced into the 5-position of the pyridine ring by selecting a suitable iodine source and reaction conditions, which can also achieve the purpose of synthesizing 2-amino-5-iodine-3-methylpyridine.
In addition, there are methods for gradually constructing target molecules by using other compounds with similar structures as starting materials through multi-step reaction conversion. However, no matter what route is used, the conditions of each step of the reaction, such as temperature, pressure, solvent, catalyst, etc., need to be finely regulated to improve the yield and selectivity of the reaction and achieve the goal of efficient synthesis of 2-amino-5-iodine-3-methylpyridine.
What are the physical properties of 2-amino-5-iodo-3-picoline?
2-Amino-5-iodo-3-picoline is an organic compound. Its physical properties are particularly important, and it is related to its performance in various chemical processes and practical applications.
First of all, its appearance is often crystalline. This is a common physical form of many organic compounds. The crystalline shape gives it a certain ordered structure, which affects its many properties. Its color may be white to off-white, and in a pure state, this color indicates its high chemical purity.
As for the melting point, this compound has a specific melting point value, which is a key indicator for identification and purification. The determination of the melting point can help chemists confirm its purity. If it contains impurities, the melting point may be deviated, and the melting range will also change.
In terms of solubility, it has a certain solubility in organic solvents, such as ethanol, dichloromethane, etc. This property is crucial in the selection of reaction media, separation and purification steps in organic synthesis. It can be soluble in specific organic solvents, so that the reaction can be carried out efficiently in a homogeneous system, improving the reaction efficiency and product yield.
Its density is also one of the important physical properties. Density reflects the mass of a substance per unit volume, and is of great significance in the measurement of materials in chemical production, the mixing process, and the operation involving phase separation. Accurate knowledge of its density can ensure the accuracy and safety of the production process.
In addition, the stability of the compound cannot be ignored. Under normal temperature and pressure, there is a certain chemical stability, but it is subject to high temperature, strong oxidizing agent or specific reaction conditions, or chemical changes. Understanding its stability helps to take appropriate measures to ensure its chemical properties during storage, transportation and use, and to ensure its application effect.
In short, the physical properties of 2-amino-5-iodo-3-picoline play a key role in organic chemistry research, chemical production and related fields. Chemists must investigate in detail before they can make good use of this compound.
What is the market outlook for 2-amino-5-iodo-3-picoline?
2 - amino - 5 - iodo - 3 - picoline is one of the organic compounds. Its market prospect is related to many factors, and it needs to be carefully observed from various angles.
First of all, this compound is often the key raw material for the creation of new drugs in the field of medicinal chemistry. In today's world, the demand for medicine is booming, and the prevention and treatment of diseases and health maintenance depend on the development of new drugs. If 2 - amino - 5 - iodo - 3 - picoline can provide a way for the synthesis of new drugs and show miraculous effects in the treatment of intractable diseases, its demand will increase greatly. As in the past, the research and development of new drugs has benefited from many unique compounds, which is also expected to follow in its footsteps, and the market prospect is promising.
Furthermore, in the genus of materials science, it may be used for the creation of special materials. Today's materials are developing rapidly, and fields such as optoelectronic materials and functional polymer materials are eager for novel compounds. If this compound can give materials unique properties after research, such as excellent electrical conductivity and optical properties, it must have a place in the materials market.
However, there are also challenges. Its synthesis process may be complex and expensive, so it will become an obstacle to large-scale production and marketing activities. Just like the process difficulties in "Tiangong Kaiwu", it is not easy to promote. And the market competition may be fierce, if there are similar alternative compounds, they will also be divided into their market shares.
In summary, 2 - amino - 5 - iodo - 3 - picoline has addressable market opportunities and may emerge in the fields of medicine and materials. However, if you want to expand the market, you need to overcome the problem of synthesis cost and demonstrate unique advantages in order to stand out in the market competition and win broad prospects.