2 Fluorobenzyl Hydrazine
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
(2-fluorobenzyl)hydrazine
Chemical Formula C7H9FN2
Molecular Weight 140.16
Appearance Typically a solid
Odor Unknown, likely has a characteristic amine - like odor
Solubility Soluble in polar organic solvents like ethanol, methanol, slightly soluble in water
Density Estimated around 1.1 - 1.2 g/cm³
Flash Point Estimated, potentially around 90 - 110 °C
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C7H9FN2
Molar Mass 140.16 g/mol
Solubility In Water Limited solubility expected, as it's an organic compound with non - polar benzene ring
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Chemical Formula C7H9FN2
Molecular Weight 140.16
Appearance Solid (likely white or off - white powder)
Odor May have a faint, characteristic amine - like odor
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, methanol, dichloromethane
Melting Point Varies, but typically in a certain temperature range
Boiling Point Under normal conditions, has a boiling point at a specific temperature
Density Specific density value (g/cm³)
Flash Point Definite flash point value (°C)
Stability Stable under normal storage conditions, may react with strong oxidizing agents
Chemical Formula C7H9FN2
Molecular Weight 140.16
Appearance Solid (usually)
Physical State At Room Temperature Solid
Odor Typically has a characteristic organic odor
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Melting Point Data varies, specific value depends on purity
Boiling Point Data varies, specific value depends on purity
Density Data may be available in literature based on experimental determination
Stability Can be relatively stable under normal conditions, but may react with strong oxidizing agents
FAQ

What are the chemical properties of (2-fluorobenzyl) hydrazine?

(2-Fluorobenzyl) hydrazine is a class of organic compounds. Its chemical properties are unique and have several remarkable characteristics.

First, (2-fluorobenzyl) hydrazine contains an active hydrazine group (-NHNH ²). The nitrogen atom in this hydrazine group has lone pairs of electrons, which makes it alkaline. Although its alkalinity is not extremely strong, it can react with acids in a suitable acid-base environment to form corresponding salts. For example, in the case of inorganic acids such as hydrochloric acid, (2-fluorobenzyl) hydrazine hydrochloride can be formed. This reaction is based on the principle of acid-base neutralization and is combined by ionic bonds. < Br >
Furthermore, due to the benzyl structure of the compound, and the hydrogen atom on the benzyl α-carbon is affected by the benzene ring and hydrazine group, it has certain activity. Under specific conditions, this α-hydrogen can be substituted. For example, in the context of suitable catalysts and reactants, nucleophilic substitution can occur and be replaced by other functional groups, thereby deriving a variety of compounds, which greatly expand its application in the field of organic synthesis.

At the same time, the fluorine atom in (2-fluorobenzyl) hydrazine also affects its properties. Fluorine atoms have high electronegativity and can affect the electron cloud density distribution of surrounding atoms through induction effects. This effect changes the polarity of the molecule, which in turn affects its physical properties such as solubility and boiling point. In some chemical reactions, the presence of fluorine atoms can affect the reactivity and selectivity, or promote the reaction to proceed in a specific direction, providing a unique pathway and possibility for organic synthesis.

In addition, due to the reductive nature of hydrazine, (2-fluorobenzyl) hydrazine can be used as a reducing agent to participate in many redox reactions. Under appropriate conditions, it can reduce some metal ions to metal elementals, or reduce compounds containing high-valent elements to low-valent states, showing its unique chemical activity and application value in redox systems.

What are the common uses of (2-fluorobenzyl) hydrazine?

(2-Fluorobenzyl) hydrazine is a crucial raw material in organic synthesis and has a wide range of common uses. In the field of medicinal chemistry, this substance is often a key intermediate. In the process of drug development, with its unique chemical structure, it can be combined with specific biological targets to exert pharmacological activity. For example, in the study of anti-tumor drugs, (2-fluorobenzyl) hydrazine participates in the construction of compounds with the ability to target tumor cells, helping to precisely attack tumor cells and reduce damage to normal cells.

In the field of materials science, (2-fluorobenzyl) hydrazine also has outstanding performance. When preparing high-performance polymer materials, it can be used as a crosslinker or modifier. After adding this substance, the mechanical properties, thermal stability and chemical stability of the polymer can be significantly improved. For example, some special materials used in the aerospace field can be modified by (2-fluorobenzyl) hydrazine to maintain excellent properties in extreme environments.

In addition, in pesticide chemistry, (2-fluorobenzyl) hydrazine is also an important synthetic block. It can be used to synthesize pesticides with high insecticidal, bactericidal or herbicidal effects. Due to its chemical activity, it can react with a variety of organic compounds to generate novel pesticide molecules, enhancing the control effect of pesticides on pests while reducing the adverse effects on the environment.

Furthermore, in the basic research of organic synthetic chemistry, (2-fluorobenzyl) hydrazine is a commonly used reagent to help scientists explore new chemical reaction pathways and mechanisms. Through its participation in the reaction, complex organic molecular structures can be constructed, providing new ideas and methods for the development of organic synthetic chemistry.

What is the synthesis method of (2-fluorobenzyl) hydrazine?

The synthesis of (2-fluorobenzyl) hydrazine is a key problem in organic synthetic chemistry. To prepare this substance, the following methods are often followed.

The first way is to react with hydrazine from 2-fluorobenzyl halide. Take an appropriate amount of 2-fluorobenzyl halide and place it in a clean reactor. Using alcohols as solvents, such as ethanol or methanol, slowly add hydrazine to the alcoholic solution at an appropriate temperature. In this reaction, the halogen atom is replaced by hydrazine to form (2-fluorobenzyl) hydrazine. However, this process requires precise temperature control. If the temperature is too high, side reactions will occur, and if it is too low, the reaction will be slow. In general, the reaction temperature should be controlled between 40 and 60 degrees Celsius, and continuous stirring is required to promote the full reaction.

The next step can be derived from 2-fluorobenzoic acid. First, 2-fluorobenzoic acid is converted into its acid chloride, and thionyl chloride is used as a chlorinating agent. Under appropriate conditions, 2-fluorobenzoyl chloride can be obtained. Subsequently, 2-fluorobenzoyl chloride is reacted with hydrazine to form (2-fluorobenzoyl) hydrazine first, and then through reduction steps, such as treatment with reducing agents such as sodium borohydride, the carbonyl group can be reduced to finally obtain (2-fluorobenzyl) hydrazine. Although this path is slightly complicated, the reaction conditions are relatively mild and the yield is relatively considerable.

In addition, the phase transfer catalysis method can be used. A phase transfer catalyst, such as quaternary ammonium salts, is added to the reaction system. A two-phase system is composed of water and an organic solvent, 2-fluorobenzyl halide is in the organic phase, and hydrazine is in the aqueous phase. The phase transfer catalyst can promote the reactants to cross the two-phase interface and accelerate the reaction process. This method can improve the reaction efficiency, shorten the reaction time, and does not require high reaction equipment. It is easy to operate.

The above methods have their own advantages and disadvantages. In actual synthesis, careful choices should be made according to factors such as raw material availability, cost considerations, and product purity requirements.

What are the physical properties of (2-fluorobenzyl) hydrazine?

(2-Fluorobenzyl) hydrazine is one of the organic compounds. Its physical properties are quite critical, and I will describe them in detail today.

Looking at its properties, under normal temperature and pressure, (2-fluorobenzyl) hydrazine is mostly colorless to light yellow liquid. When the texture is pure, the appearance is clear and transparent. If you sense it by smell, it has a special smell. However, this smell is not pungent and intolerable, but it is also unique and recognizable.

As for the melting point, the value of the melting point is about - [X] ° C. Under this low temperature, the substance changes from liquid to solid. The boiling point is around [X] ° C. At this temperature, the substance jumps from the liquid state to the gaseous state. Such melting boiling point characteristics make (2-fluorobenzyl) hydrazine exist in the liquid state in ordinary environments.

In terms of solubility, it exhibits good solubility in organic solvents such as ethanol and ether. This is because there are suitable interactions between the molecular structure of (2-fluorobenzyl) hydrazine and the molecules of organic solvents, such as van der Waals force, hydrogen bond, etc., so it can be fused seamlessly. However, in water, its solubility is relatively limited, because the polarity of water and the polarity of (2-fluorobenzyl) hydrazine molecules are different, and the two are difficult to fully miscible. < Br >
Density is also one of its important physical properties. The density of (2-fluorobenzyl) hydrazine is slightly higher than that of water, about [X] g/cm ³. This property makes it possible for liquids with different densities (2-fluorobenzyl) hydrazine and water to be naturally stratified in some scenarios involving liquid-liquid separation, which facilitates the separation and purification of substances.

In addition, the volatility of (2-fluorobenzyl) hydrazine is relatively moderate. Although it is not highly volatile, its molecules can gradually escape into the surrounding space under certain conditions, such as rising temperature and good ventilation. This volatility places certain requirements on its storage and use environment, and it needs to be properly sealed and stored to prevent its volatilization loss, and it should be carried out in a well-ventilated place during use to ensure safety.

What are the precautions for (2-fluorobenzyl) hydrazine during use?

For (2-fluorobenzyl) hydrazine, many matters need to be paid attention to when using it. This is a chemical substance and has certain dangers. The first thing to pay attention to is its toxicity. If it is accidentally ingested, inhaled or touched the skin, it may cause damage to the body. Therefore, when operating, be sure to take good protection, such as wearing suitable protective gloves, masks and goggles, to prevent its harm.

In addition, its chemical properties are active and easy to react with other substances. In terms of storage, it should be placed in a cool, dry and well-ventilated place, away from fire, heat and oxidizing substances to prevent unexpected reactions from causing danger, such as fire and explosion.

Repeat, during use, the established operating procedures and experimental steps must be strictly followed. Do not change the dosage and reaction conditions at will to prevent the reaction from getting out of control. And the operation should be carried out in a fume hood, so that the harmful gases that may be generated can be drained in time to ensure the safety of the environment and the operator.

In addition, after use, the remaining (2-fluorobenzyl) hydrazine and related waste must not be discarded at will, and should be properly disposed of in accordance with the prescribed methods to avoid pollution to the environment. In short, when using this material, it is necessary to be cautious and always pay attention to safety and norms to ensure that everything goes smoothly and avoid disasters.