Chemical Formula | C7H6ClFO |
Molar Mass | 160.57 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 214 - 216 °C |
Density | 1.338 g/cm³ |
Flash Point | 102 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Purity | Typically high - purity grades available |
Chemical Formula | C7H6ClFO |
Molar Mass | 160.57 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | Around 220 - 225 °C |
Solubility In Water | Poorly soluble in water |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | Data may vary, but potentially flammable liquid with appropriate flash point |
Purity | Typically sold with high purity (e.g., 97%+ in commercial products) |
What are the chemical properties of 5-chloro-2-fluorobenzyl alcohol?
5-Alkane-2-enheptanal, an organic compound, has unique chemical properties and has important uses in many chemical reactions and chemical production fields. The following details its chemical properties:
** First, the properties of aldehyde groups **
1. ** Oxidation reaction **: The aldehyde group is easily oxidized. In case of weak oxidants, such as silver ammonia solution, under the heating condition of a water bath, 5-alkane-2-enheptanal will undergo a silver mirror reaction. The aldehyde group is oxidized to a carboxyl group to precipitate metallic silver. This reaction can be used to identify aldehyde compounds. When co-heated with the new copper hydroxide suspension, the aldehyde group is also oxidized, and the copper hydroxide is reduced to a cuprous oxide red precipitate. In case of strong oxidants, such as acidic potassium permanganate solution, not only the aldehyde group will be oxidized to carboxylic groups, but the carbon-carbon double bond may also be oxidized, resulting in molecular structure changes.
2. ** Reduction Reaction **: The aldehyde group can be added to hydrogen in the presence of a catalyst (such as nickel, etc.) to generate corresponding alcohols. After the addition of 5-alkane-2-enheptanal to hydrogen, the aldehyde group is converted into a hydroxyl group to obtain 5-alkane-2-enheptanol. This reaction is an important method for the preparation of alcohols.
3. ** Condensation reaction **: Condensation reaction can occur with compounds containing active hydrogen. For example, with alcohols under the action of acidic catalysts, hemiacetal is formed first, and then acetal is formed. 5-alkane-2-enheptanal reacts with ethanol to form 5-alkane-2-enheptanal acetal. This reaction is often used to protect aldehyde groups in organic synthesis.
** Second, the properties of carbon-carbon double bonds **
1. ** Addition reaction **: Carbon-carbon double bonds can be added with a variety of electrophilic reagents. For example, when reacting with bromine water, the bromine atoms in the bromine elemental substance are added to the two carbon atoms of the carbon-carbon double bond, fading the bromine water and generating halogenated hydrocarbons containing bromine atoms. When adding with hydrogen chloride, follow the Markov rule, hydrogen atoms are added to the double-bond carbon atoms containing more hydrogen, and chlorine atoms are added to the double-bond carbon atoms containing less hydrogen to obtain the corresponding halogenated hydrocarbons.
2. ** Oxidation reaction **: In addition to being oxidized by acidic potassium permanganate solution mentioned above, it can also be oxidized by ozone under specific conditions. Ozone reacts with carbon-carbon double bonds to form odorous oxides. After reductive hydrolysis, the double bonds are broken. According to the different positions and structures of the double bonds, products such as corresponding aldodes, ketones or carboxylic acids are generated.
3 ** Polymerization reaction **: Under the action of the initiator, the compounds containing carbon-carbon double bonds can undergo polymerization. 5-alkane-2-enheptanal may also undergo polymerization in theory to form a polymer, which may have potential application value in the preparation of special polymer materials.
What are the physical properties of 5-chloro-2-fluorobenzyl alcohol?
The physical properties of 5-% -2-alkylthiofuran are as follows:
Its external properties are usually liquid or solid, depending on the chemical properties and the surrounding conditions. Under normal conditions, some compounds are colored to light-colored liquid, while some exist in the form of solid crystals.
5-% -2-alkylthiofuran has certain properties. Because its molecules contain alkylthio atoms, its properties are different from those of ordinary compounds. The introduction of alkyl atoms increases the molecular force, and in general, its performance is reduced compared with that of alkyl groups. The presence of alkyl thio groups also affects the properties of alkyl thio groups. Factors such as the degree of carbon and branching of alkyl thio groups all change the Vander force of molecules and affect the properties of molecules.
The melting force of compounds is affected by the influence of molecules. The high performance of atoms can make molecules form an even-even interaction, resulting in an increase in the melting force. The increase of carbon in alkyl thio groups and the increase of the Vander force of molecules also promote the increase of the melting force. Therefore, 5-% -2-alkanthiofurans with different substituents have a certain degree of solubility.
In terms of solubility, 5-% -2-alkanthiofurans have a certain solubility in soluble solutions, such as ethanol, ethyl ether, acetone, etc. The solubility of the phase in water is low, and the ratio of the hydrophobic part is even higher. However, compared with the completely hydrophobic phase, it is slightly higher due to the presence of atoms.
Its density is also closely related to the molecular phase. The atomic weight of the atom is large, and the introduction into the molecule increases the overall density; the density of alkanthio groups also has an impact, and the density of 5-%-2-alkanthiofurans is usually higher than that of water. In the system where the atomic weight of the atom and the aqueous phase coexist, it is often lower.
What are the main uses of 5-chloro-2-fluorobenzyl alcohol?
5-Ammonia-2-hydroxybenzoic acid, also known as anthosalicylic acid, has a wide range of main uses.
In the field of medicine, this is an important pharmaceutical intermediate. It is often used as the starting material for the synthesis of many antibacterial and anti-inflammatory drugs. For example, some therapeutic drugs for intestinal inflammatory diseases use the special chemical structure of 5-ammonia-2-hydroxybenzoic acid to construct drug active ingredients through a series of chemical reactions, so as to play a role in alleviating and treating intestinal inflammation.
In the dye industry, 5-ammonia-2-hydroxybenzoic acid also plays a key role. Due to the presence of reactive groups such as amino and hydroxyl groups in its structure, it can participate in many dye synthesis reactions. Through specific processes, dyes with bright color and good stability can be prepared, which are widely used in textile printing and dyeing and other industries to give fabrics rich and colorful colors.
In the field of chemical research, 5-ammonia-2-hydroxybenzoic acid is often used as a key reagent in organic synthesis due to its unique chemical properties. Researchers use it as a basis to explore and study various organic reactions, to help the synthesis of new compounds and the in-depth exploration of reaction mechanisms, and to provide support for the development of organic chemistry.
To sum up, 5-ammonia-2-hydroxybenzoic acid is indispensable in the fields of medicine, dyes and chemical research, and is of great significance to the development of related industries.
What are the synthesis methods of 5-chloro-2-fluorobenzyl alcohol?
To prepare 5-bromo-2-pentanone, the following methods can be used:
First, use 2-pentanone as the starting material. In 2-pentanone, the hydrogen on the α-carbon connected to the carbonyl group has a certain activity due to the influence of the carbonyl group. It can be substituted with bromine under the action of a suitable catalyst such as an acid or base. If an acid is used as a catalyst, the acid first protonates the carbonyl oxide, enhances the electron-absorbing effect of the carbonyl group on α-carbon, and makes α-hydrogen more likely to leave. In this environment, the bromine molecule cracks into positive bromide ions and negative bromide ions, and the positive bromide ions attack α-carbon to form 5-bromo-2-pentanone. The reaction conditions are relatively mild and the reaction is easy to control, but there may be polybromination by-products, and the amount of bromine and the reaction time need to be strictly controlled.
Second, it is prepared by the reaction of 1,4-pentadiene with hydrogen bromide and carbon monoxide. 1,4-pentadiene has a conjugated double bond, which can undergo electrophilic addition reaction with hydrogen bromide. During this process, due to the existence of the conjugated system, different addition products will be produced. At the same time, carbon monoxide can participate in the reaction under suitable catalyst and reaction conditions, and finally generate 5-bromo-2-pentanone through a series of complex transformations. The raw materials of this method are relatively common, but the reaction involves a variety of reactants and complex reaction mechanisms, which require high reaction equipment and conditions.
Third, γ-pentanolactone is used as the raw material. Gamma-pentanolactone first opens the ring under appropriate conditions, and the lactone ring can be opened to form a compound with suitable functional groups by reacting with specific reagents. After that, bromine atoms are introduced through halogenation reaction, and then other groups are gradually converted into carbonyl groups through functional group conversion, thereby obtaining 5-bromo-2-pentanone. This route has relatively many steps, but the selectivity of each step is well controlled, and the yield of the target product can be improved by fine regulation of the reaction conditions.
What are the precautions for storing and transporting 5-chloro-2-fluorobenzyl alcohol?
In the process of storage, 5-%-2-alkylthiofuran needs to pay attention to the general situation.
Its performance is not good, and it is the first thing to survive. If the environment is wet, the action of water vapor is easy to cause the reaction of hydrolysis, etc., which will destroy its own damage and affect the product. Therefore, it is appropriate to use the environment where the atmosphere is dry to prevent the damage of moisture.
The temperature is also low. This material is sensitive to multiple degrees. Under high temperatures, it may cause decomposition, polymerization and other reactions. Therefore, it is usually best to keep the temperature below 20 ° C. It must not be exposed to the hot sun or high temperatures.
Furthermore, it has certain properties, and some substances may be harmful. Therefore, the storage container must be well sealed to prevent leakage, not only to ensure that the content of the material itself is not low, but also to avoid the harm caused by the surrounding environment of the material.
In addition, the packaging is very important. It is necessary to use a combination of packaging materials, which can withstand a certain external force and prevent the container from breaking. And the packaging is resistant to corrosion, because 5-% -2-alkylthiofuran or some materials have a corrosive effect.
The packaging also needs to be kept clean and dry to avoid mixing with other chemicals. Due to its special properties, if incompatible materials are not connected, it is easy to cause dangerous reactions, such as burning, explosion, etc.
In addition, people are familiar with its dangerous characteristics and emergency treatment methods. In the event of an accident such as leakage, measures can be taken quickly and positively to reduce the harm.
In other words, whether it exists or is 5-%-2-alkylthiofuran, it is necessary to follow the phase and pay attention to each product to ensure its safety.