The product is Factory Supply 1-bromo-3,5-difluorobenzene with the CAS number 461-96-1. It is offered at a low price, which makes it an attractive option for various applications. The chemical formula of 1-bromo-3,5-difluorobenzene is C₆H₃BrF₂. It has a molecular weight that can be calculated based on the atomic masses of carbon, hydrogen, bromine, and fluorine. This compound is a type of aromatic organic compound, which has a characteristic benzene ring structure with bromine and fluorine substituents.
Physically, it may appear as a liquid or solid with specific melting and boiling points depending on its purity and other factors. The purity of the product from the factory supply is an important parameter. High - purity 1-bromo-3,5-difluorobenzene is often preferred in many chemical reactions to ensure accurate and reproducible results.
1-bromo-3,5-difluorobenzene has a wide range of uses in the chemical industry. It is commonly used as a building block in organic synthesis. In the pharmaceutical field, it can be used as an intermediate for the synthesis of various drugs. The unique combination of bromine and fluorine atoms on the benzene ring gives it special reactivity, which can be utilized to introduce specific functional groups into drug molecules.
In the field of materials science, it can be used in the synthesis of advanced polymers. These polymers may have special properties such as high chemical resistance, good thermal stability, or unique optical properties. The fluorine atoms in the molecule can enhance the hydrophobicity and chemical stability of the polymers, while the bromine atom can be used as a reactive site for further modification or cross - linking.
When using 1-bromo-3,5-difluorobenzene, proper safety precautions should be taken. It is recommended to handle it in a well - ventilated laboratory or industrial environment. Personal protective equipment such as gloves, safety glasses, and a lab coat should be worn. Before use, the product should be carefully inspected for any signs of contamination or degradation.
In chemical reactions, the amount of 1-bromo-3,5-difluorobenzene used should be accurately measured according to the reaction requirements. It can be added to the reaction system in various ways, such as by using a syringe or a pipette in small - scale laboratory reactions, or through automated feeding systems in large - scale industrial processes. The reaction conditions, including temperature, pressure, and reaction time, should be carefully controlled to optimize the reaction outcome.
Caso 1: Síntese farmacêutica
In a pharmaceutical research project, scientists aimed to synthesize a new anti - cancer drug. They used 1-bromo-3,5-difluorobenzene as an intermediate. First, they reacted it with a specific amine compound in the presence of a suitable catalyst. The reaction was carried out at a moderate temperature of around 80°C for several hours under an inert gas atmosphere. After purification through column chromatography, they obtained an intermediate product with the desired structure. This intermediate was then further reacted with other reagents to form the final anti - cancer drug. The use of 1-bromo-3,5-difluorobenzene provided a key step in introducing the necessary fluorine and bromine - containing groups into the drug molecule, which was crucial for its biological activity.
Caso 2: Síntese de polímeros
In a materials science laboratory, researchers were working on developing a new type of high - performance polymer for use in electronic devices. They used 1-bromo-3,5-difluorobenzene as a monomer in a polymerization reaction. The polymerization was carried out in a solution of an organic solvent at a relatively low temperature. The bromine atoms on the 1-bromo-3,5-difluorobenzene molecule were able to react with other monomers to form a polymer chain. The resulting polymer had excellent chemical resistance and thermal stability, which made it suitable for use in protecting electronic components from harsh environments.
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Este é o William, Diretor Executivo da Zhishang Chemical Co., Ltd.
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