1 Benzyloxy 2 Fluoro Benzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-BENZYLOXY-2-FLUORO-BENZENE
Chemical Formula C13H11FO
Molecular Weight 202.224 g/mol
Appearance Liquid (predicted)
Boiling Point 291.9 °C at 760 mmHg (predicted)
Density 1.122 g/cm³ (predicted)
Vapor Pressure 0.00201 mmHg at 25 °C (predicted)
Logp 3.98 (predicted)
Flash Point 123.3 °C (predicted)
Solubility Soluble in organic solvents like ethanol, dichloromethane (general properties of similar aromatic compounds)
Chemical Formula C13H11FO
Molecular Weight 202.224 g/mol
Appearance Colorless to light yellow liquid
Boiling Point Around 275 - 280 °C
Density Approx. 1.13 g/cm³ (estimated)
Flash Point Around 110 - 120 °C (estimated)
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether, dichloromethane
Vapor Pressure Low at room temperature
Chemical Formula C13H11FO
Molecular Weight 202.224 g/mol
Appearance Colorless to light yellow liquid
Boiling Point Approximately 280 - 285 °C
Density Approx. 1.12 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point Around 122 °C
Odor Aromatic odor
FAQ

What are the main uses of 1-benzyloxy-2-fluorobenzene?

1-Hydroxyamino-2-chloronaphthalene, this substance is a chemical substance. Its main uses are complex. Although it has not been specifically recorded in the "Tiangong Kaiwu", it can be inferred from current chemical knowledge and the development of past chemical uses.

In the dye industry, 1-hydroxyamino-2-chloronaphthalene can be used as a key intermediate. The manufacture of dyes often relies on the delicate reaction of a variety of organic compounds. The special structure of this substance can introduce various chromophores through specific chemical reactions, resulting in colorful dyes with different properties. For example, azo dyes with excellent light resistance and washable fastness can be generated by condensation with certain nitrogenous and sulfur-containing compounds, which are widely used in fabric printing and dyeing to make fabrics lasting and bright.

In the field of pharmaceutical synthesis, 1-hydroxyamino-2-chloronaphthalene also plays an important role. The development and synthesis of drugs requires the precise construction of molecular structures to meet the specific physiological activity requirements. The structural properties of this compound make it a starting material or a key intermediate for the synthesis of certain drugs. For example, in the synthesis path of some anti-inflammatory and antibacterial drugs, its active groups can be used to construct complex molecular structures with specific pharmacological activities through multi-step reactions, which can help human health.

In addition, in the basic research of organic synthetic chemistry, 1-hydroxyamino-2-chloronaphthalene, as a typical organic compound, is often used to explore new reaction pathways and study reaction mechanisms. Chemists expand the boundaries of organic synthesis methodologies by in-depth exploration of the chemical reactions they participate in, providing new ideas and methods for the synthesis of more complex and high-value-added organic compounds, and promoting the continuous development of organic chemistry.

What are the physical properties of 1-benzyloxy-2-fluorobenzene?

The boron group, also known as the boron group, is an important subgroup in the chemical process, and its chemical formula is BH.

The boron group has many properties. First, it is original, and it can be charged with the original force in the multiplexing reaction, and it can make the original metal. Second, the boron group can release the original gold (Cu ²) in the water reaction energy, which has a research value, and may have a useful force in the energy phase.

The physical properties of boron are also special. Boron phase compounds are multi-solid, such as boronide (NaBH), boron phase (LiBH), etc., and their melting properties vary from compound to compound. Boron phase compounds are melted at 400 ° C, and boron phase compounds are melted at a slightly lower level, around 280 ° C. Furthermore, boron compounds have different solubility in solution. Boron compounds have a certain solubility in soluble solutions such as methanol and ethanol, while boron compounds can also be dissolved to a certain extent in non-soluble solutions such as ether. In addition, boron compounds are mostly white or exochromatic, boron compounds are white small crystalline powders, and boron compounds are also white crystals. Therefore, the physical and chemical properties of boron compounds and their phase compounds make them have important uses in chemical synthesis, material manufacturing, energy and other fields.

What are the chemical properties of 1-benzyloxy-2-fluorobenzene?

1-Hydroxy-2-naphthalaldehyde, this is an organic compound with unique chemical properties.

One of its chemical properties is that it has two types of active functional groups: aldehyde group and phenolic hydroxyl group. The aldehyde group can undergo many reactions, such as acetal reaction with alcohols catalyzed by acids. Although this specific compound is not described in detail in Tiangong Kaiwu, it can be used as an analogy at the level of chemical reaction principles. In ancient times, it was known that the reaction of metals with acids, such as "iron with acetate, iron filings", is the reaction of iron with acetic acid. Similarly, the aldehyde group of 1-hydroxy-2-naphthalaldehyde is prone to react when it encounters a compound with active hydrogen. The aldehyde group can also undergo oxidation reaction, and under the action of mild oxidizing agents, it can be converted into carboxyl groups, just like some substances in ancient alchemy were oxidized in the air.

Phenolic hydroxyl groups also give it special properties. Phenolic hydroxyl groups have certain acidity and can react with bases to form salts. This is like the reaction of plant ash water (containing basic substances such as potassium carbonate) with some acidic substances mentioned in Tiangong Kaiwu. The phenolic hydroxyl groups of 1-hydroxy-2-naphthalene formaldehyde can react with alkali metal hydroxides to form corresponding phenolic salts. Phenolic hydroxyl groups are also prone to substitution reactions. Due to the activation of phenolic hydroxyl groups on the benzene ring, the activity of adjacent and para-hydrogen atoms on the benzene ring is enhanced, and they are easily replaced by halogen atoms, nitro groups and other substituents. It is similar to the precise processing of specific parts of the material by craftsmen in ancient times, replacing some of the elements.

In addition, 1-hydroxy-2-naphthalene formaldehyde has certain stability and unique spectral properties due to the conjugate system in the molecule. The conjugate system deloculates electrons and reduces the molecular energy. Although this was not directly described in ancient times, it can be compared to the stability of the building structure. The conjugate system is like a stable structure, supporting the stability of molecules. Its spectral properties can be used for analysis and identification. Although there was no modern spectral analysis technology in ancient times, there are similarities in the cognition and distinction of material characteristics, that is, it can be identified by observing the unique performance of substances.

What are the synthesis methods of 1-benzyloxy-2-fluorobenzene?

The synthesis method of 1-hydroxyamino-2-chloronaphthalene has been used by many parties throughout the ages. Now I will come to you one by one.

First, start with naphthalene, first through halogenation, introduce chlorine atoms into the naphthalene ring to obtain chloronaphthalene. Then, through nitrification, nitro is introduced at an appropriate position. This step requires careful selection of reaction conditions, such as temperature and the ratio of reagents, so that the nitro is just what is needed. Then with an appropriate reducing agent, such as iron filings mixed with hydrochloric acid, or catalytic hydrogenation, the nitro group is reduced to an amino group. However, the amino group is not a hydroxylamino group, and a special reaction is required to use a suitable reagent, such as sodium nitrite and an acidic medium, to convert the amino group into a hydroxylamino group, and finally obtain 1-hydroxyamino-2-chloronaphthalene.

Second, it can also be started from other compounds containing chlorine and naphthalene. For example, some chloronaphthalene derivatives with specific substituents can be achieved by the conversion of functional groups. First, the existing substituents are modified to convert them into active groups that can be further reacted. Then, through a series of reactions, such as nucleophilic substitution, redox, etc., the hydroxyamino group is gradually constructed. This path requires a precise grasp of the properties and reactivity of the existing compounds, and clever design of the reaction steps to be able to synthesize smoothly.

Third, there is also a method of using organometallic reagents. The halogenate containing chlorine naphthalene reacts with suitable organometallic reagents, such as Grignard reagent, to form a carbon-carbon bond or a carbon-hetero bond. After subsequent reactions, the amino part is introduced, which is then converted into a hydroxyamino group. In this way, the preparation and use of organometallic reagents need to be handled with caution, because of their high activity and strict requirements on the reaction environment.

All kinds of synthesis methods have their own advantages and disadvantages. It is necessary to weigh and choose according to actual conditions, such as the availability of raw materials, the difficulty of reaction, and cost considerations, in order to achieve the purpose of synthesis.

What should be paid attention to when storing and transporting 1-benzyloxy-2-fluorobenzene?

1 - phenolic hydroxyl group is an important functional group in organic compounds and has active chemical properties. Its hydrogen atoms are easier to dissociate, making the phenolic hydroxyl group compounds acidic to a certain extent, and can react with a variety of reagents, such as reacting with sodium metal to generate hydrogen gas and reacting with bases to form salts. Phenolic hydroxyl groups can also participate in esterification reactions, substitution reactions and many other organic reactions, and play a significant role in the field of organic synthesis.
2 - ethylene oxide should be stored and transported with caution. This is because it is highly dangerous. When storing, it is advisable to choose a cool and ventilated warehouse, away from fire and heat sources. Because it is flammable and can form explosive mixtures when mixed with air, it can cause combustion and explosion in case of open flame and high heat. The temperature of the warehouse should not exceed 30 ° C, and direct sunlight should be protected. At the same time, it should be stored separately from acids, alkalis, alcohols, etc., and should not be mixed.

During transportation, the transportation vehicle should be equipped with the corresponding variety and quantity of fire-fighting equipment and leakage emergency treatment equipment. It is best to transport in the morning and evening in summer to prevent sunlight exposure. During transportation, ensure that the container does not leak, collapse, fall, or damage. The trough (tank) car used during transportation should have a grounding chain, and holes can be set in the trough to reduce shock and generate static electricity. It is strictly forbidden to mix with acids, alkalis, alcohols, edible chemicals, etc. During transportation, it should be protected from exposure to the sun, rain, and high temperature. Road transportation should follow the specified route and do not stop in residential areas and densely populated areas. Overall, the storage and transportation of ethylene oxide requires strict compliance with relevant safety regulations to ensure the safety of personnel and the environment.