Chemical Formula | C7H5BrClF |
Molar Mass | 225.47 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | Approximately 245 - 247 °C |
Solubility | Soluble in organic solvents like dichloromethane, chloroform |
Purity | Typically sold in high purity grades, e.g., 95%+ |
Odor | Pungent, characteristic of halogenated organic compounds |
Name | 2-Bromo-5-fluorobenzyl chloride |
Molecular Formula | C7H5BrClF |
Molar Mass | 223.47 g/mol |
Appearance | Colorless to light yellow liquid |
Density | 1.667 g/cm³ |
Boiling Point | 214 - 216 °C |
Melting Point | N/A |
Solubility | Insoluble in water, soluble in organic solvents like ethanol, ether |
Flash Point | 93.4 °C |
Refractive Index | 1.565 |
Cas Number | 364-34-1 |
What are the physical properties of 2-Bromo-5-fluorobenzylchloride?
2-Bromo-5-fluorobenzyl chloride is an important compound in the field of organic chemistry. It has unique physical properties and is described in detail as follows:
Looking at its properties, 2-bromo-5-fluorobenzyl chloride is usually colorless to pale yellow liquid at room temperature and pressure. This form gives it a certain degree of fluidity, making it relatively convenient for many chemical operations, such as dumping and transfer. However, it should be noted that because it is a liquid, when storing and using, it requires quite high sealing of the container to prevent it from evaporating and escaping.
The boiling point of this compound is about a specific temperature range. The physical property of boiling point is of great significance in the process of separation and purification of compounds. By precisely controlling the temperature and taking advantage of the difference in boiling points, 2-bromo-5-fluorobenzyl chloride can be effectively separated from the mixed system to achieve the purpose of purification.
Its melting point also has a specific value. The melting point characterizes the critical temperature at which a substance transitions from solid to liquid. Knowing the melting point helps to determine the purity of the compound. If the purity of the compound is high, its melting point is usually more acute and the melting range is narrow; conversely, if it contains impurities, the melting point may be reduced and the melting range will also be wider.
The density of 2-bromo-5-fluorobenzyl chloride is also an important physical parameter. Compared with water, its density shows a specific relationship. This property is crucial in experimental operations involving liquid-liquid separation. Depending on the density difference, a suitable method can be selected to effectively separate 2-bromo-5-fluorobenzyl chloride from other liquids.
Furthermore, the solubility of this compound cannot be ignored. It exhibits a certain solubility in common organic solvents such as ethanol, ether, dichloromethane, etc. This property provides a basis for the choice of solvents in organic synthesis reactions. Suitable solvents not only promote the dissolution of reactants, increase the chance of intermolecular collisions, speed up the reaction rate, but also may affect the reaction selectivity. The physical properties of 2-bromo-5-fluorobenzyl chloride are of great significance in many fields such as organic synthesis and chemical analysis. Only by deeply understanding and making good use of these properties can we carry out related chemical work more efficiently.
What are the chemical properties of 2-Bromo-5-fluorobenzylchloride?
2-Bromo-5-fluorobenzyl chloride is also an organic compound. It has the characteristics of halogenated aromatics, is active, and can be used as a key raw material in many organic reactions.
In this compound, both bromine and fluorine atoms are electronegative, causing the electron cloud density of the benzene ring to be modulated, and the activity is different from that of the ordinary benzene ring. The chlorine atom of the benzyl chloride part has the activity of nucleophilic substitution reaction. In the case of nucleophilic reagents, the chlorine atom is easily replaced to form a new carbon-heteroatom bond. For example, when catalyzed by bases with alcohols, ether compounds can be generated; when reacted with amines, it forms an amine substitution product < Br >
And bromine atoms are not idle. They can be combined with other organoborides or organostannides through metal-catalyzed cross-coupling reactions, such as Suzuki reaction, Stein reaction, etc., to build more complex molecular structures. It is widely used in the fields of drug synthesis and materials chemistry.
The introduction of fluorine atoms can affect the physical, chemical and biological activities of molecules due to the unique electronic properties of fluorine. It can often improve the lipid solubility of compounds and enhance their ability to penetrate biofilms. It may improve the absorption and distribution of drugs in drug development. < Br >
2-Bromo-5-fluorobenzyl chloride contains a variety of active halogen atoms and has diverse reactivity. It plays an important role in the field of organic synthetic chemistry and is a powerful tool for creating novel organic molecular structures.
What are the common synthetic methods of 2-Bromo-5-fluorobenzylchloride?
2-Bromo-5-fluorobenzyl chloride is also an important intermediate in organic synthesis. Its common synthesis methods cover several ends.
First, 2-bromo-5-fluorotoluene is used as the starting material. First, 2-bromo-5-fluorotoluene reacts with N-bromosuccinimide (NBS) in the presence of an initiator. This initiator is often benzoyl peroxide or the like. During the reaction, light or heat is used to promote the reaction of its free radicals. NBS provides bromine radical, which captures the hydrogen atom at the 2-bromo-5-fluorotolubenzyl position, and then generates benzyl radical. This radical reacts with the bromine generated by NBS to obtain 2-bromo-5-fluorobenzyl bromide. Then, 2-bromo-5-fluorobenzyl bromide is treated with a chlorination agent such as sulfinyl chloride (SOCl ³). Sulfuryl chloride undergoes nucleophilic substitution with the bromine atom in benzyl bromide, and the chlorine atom replaces the bromine atom to obtain 2-bromo-5-fluorobenzyl chloride.
Second, 2-bromo-5-fluorobenzoic acid can also be used as the starting material. First reduce 2-bromo-5-fluorobenzoic acid to 2-bromo-5-fluorobenzyl alcohol. This reduction method can be used as a strong reducing agent such as lithium aluminum hydride (LiAlH) in anhydrous ether or tetrahydrofuran and other solvents. 2-bromo-5-fluorobenzyl alcohol is then reacted with a chlorinating agent. The commonly used chlorinating agent, in addition to thionyl chloride, can also use trichloride (PCl) and the like. Taking phosphorus trichloride as an example, it reacts with 2-bromo-5-fluorobenzyl alcohol, and the hydroxyl group is replaced by chlorine atoms to obtain 2-bromo-5-fluorobenzyl chloride.
Or, take 2-bromo-5-fluoroaniline as the starting material. After diazotization, 2-bromo-5-fluoroaniline is treated with sodium nitrite and hydrochloric acid to obtain diazonium salt. The diazonium salt is then reacted with cuprous chloride (CuCl) to undergo a Sandmeyer reaction. The diazonium group is replaced by a chlorine atom to obtain 2-chloro-1-bromo-4-fluorobenzene. After that, through the Fu-gram alkylation reaction, chloromethylation reagents, such as a mixture of formaldehyde and hydrogen chloride, are introduced under the catalysis of anhydrous zinc chloride, and finally 2-bromo-5-fluorobenzyl chloride can be obtained.
Synthesis methods have their own advantages and disadvantages. The selection of starting materials, the control of reaction conditions, and the separation and purification of products must be carefully considered in the synthesis process.
What are the main applications of 2-Bromo-5-fluorobenzylchloride?
2-Bromo-5-fluorobenzyl chloride, an organic compound, has important applications in many fields.
In the field of medicinal chemistry, its role is quite large. Because of its halogen-containing structure and unique chemical activity, it can be used as a key intermediate for the synthesis of various specific drugs. For example, through specific chemical reactions, it is connected to compounds containing heteroatoms such as nitrogen and oxygen to construct complex drug molecular structures, laying the foundation for the development of innovative drugs for the treatment of difficult diseases such as tumors and cardiovascular diseases. In the development of many anti-cancer drugs, 2-bromo-5-fluorobenzyl chloride is used as a starting material to introduce key structural fragments through multi-step reactions, which is of great significance for improving drug activity and selectivity.
In the field of materials science, it is also indispensable. It can be used as a functional monomer to participate in the synthesis of polymer materials. Through polymerization, it is introduced into the main chain or side chain of the polymer to endow the material with unique properties. For example, the preparation of polymer materials with special optical and electrical properties can be used to fabricate optoelectronic devices such as organic Light Emitting Diodes (OLEDs) and sensors. Due to its halogen atom properties, it can adjust the electron cloud distribution of the material and improve the charge transport performance and luminous efficiency of the material.
In the field of pesticide chemistry, it is also widely used. It can be used as an important raw material for the synthesis of new pesticides. Using its chemical activity, pesticides with high toxic effect on pests and environmental friendliness can be synthesized. Compared with traditional pesticides, such pesticides based on 2-bromo-5-fluorobenzyl chloride synthesis may have higher selectivity and lower residue, which can not only effectively control crop diseases and pests, but also reduce the negative impact on the ecological environment, which is in line with the current needs of green agriculture development.
To sum up, 2-bromo-5-fluorobenzyl chloride plays a crucial role in many fields such as medicine, materials, and pesticides, and is of great significance to promoting technological innovation and development in various fields.
2-Bromo-5-fluorobenzylchloride What are the precautions during storage and transportation?
2-Bromo-5-fluorobenzyl chloride is also an organic compound. When storing and transporting, it is necessary to pay attention to many matters to ensure its quality and safety.
First storage, this compound should be placed in a cool, dry and well-ventilated place. Because of the cool environment, it can reduce the risk of chemical reactions caused by excessive temperature. If it is exposed to high temperature, it may cause the compound to decompose and deteriorate, which will damage its chemical properties. The dry place is also critical because it is afraid of water, and the product is impure due to reactions such as hydrolysis or hydrolysis. Good ventilation can prevent the accumulation of harmful gases and protect the safety of the storage environment.
Furthermore, it should be stored away from fire, heat sources and oxidants. 2-Bromo-5-fluorobenzyl chloride is flammable, and the flame and heat source are close, or it may cause combustion or even explosion, which endangers the safety of the surrounding area. When the oxidant comes into contact with it, it is easy to cause violent oxidation reaction and increase danger. When storing, it should be placed separately from the oxidant, with obvious intervals and signs.
As for transportation, the packaging must be tight and stable. Wrap the compound in a suitable packaging material, such as a corrosion-resistant container, to prevent it from leaking during transportation. Leakage not only causes the loss of the compound, but also is toxic and harmful, or pollutes the environment and endangers the safety of humans and animals.
During transportation, also ensure that the temperature and humidity are stable. As mentioned earlier, abnormal temperature and humidity can cause qualitative changes of the compound. It should be equipped with corresponding temperature control and humidity control equipment to maintain suitable environmental conditions according to its characteristics.
And transportation personnel must undergo professional training, familiar with the properties of 2-bromo-5-fluorobenzyl chloride and emergency treatment methods. In case of leakage, fire and other accidents on the way, it can respond quickly and properly to minimize harm.