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3-BROMOCHLOROBENZENE CAS:108-37-2

3-Bromochlorobenzene is a halogenated aromatic compound with the molecular formula C6H4BrCl. It consists of a benzene ring with both bromine and chlorine substituents located at the meta positions relative to each other. This compound typically appears as a colorless to yellow liquid and is known for its moderate solubility in organic solvents while being less soluble in water. 3-Bromochlorobenzene plays a significant role as an intermediate in organic synthesis and is utilized in the production of pharmaceuticals, agrochemicals, and specialty chemicals due to its reactivity in electrophilic substitution reactions and nucleophilic transformations.


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Application and Effect:

3-Bromochlorobenzene (C6H4BrCl) is characterized by its unique structure comprising a benzene ring substituted with both a bromine atom and a chlorine atom at the meta positions. The presence of these halogens influences the chemical properties and reactivity of the molecule, making it valuable in various synthetic applications. As a halogenated aromatic compound, it exhibits moderate volatility and can range from a colorless liquid to a yellowish hue, depending on purity and environmental factors. The synthesis of 3-bromochlorobenzene can be achieved through several methods, including the bromination of chlorobenzene or the chlorination of bromobenzene under controlled conditions. Typically, these reactions are performed using electrophilic aromatic substitution techniques, where either bromine or chlorine acts as an electrophile, facilitated by Lewis acids like aluminum chloride (AlCl3). The regioselectivity of these reactions is crucial, as it determines the position of the substituents on the aromatic ring. In organic synthesis, 3-bromochlorobenzene serves as a versatile building block for further transformations. Its bromine and chlorine atoms provide reactive sites for nucleophilic substitution reactions, allowing for the introduction of various functional groups. For example, nucleophiles such as amines or alcohols can displace the bromine atom, leading to the formation of amines or ether derivatives, which are important in pharmaceutical development and materials science. Additionally, 3-bromochlorobenzene finds application in the production of specialized compounds used in agrochemicals and polymer chemistry. Its ability to participate in cross-coupling reactions, such as Suzuki or Heck reactions, enables the formation of complex molecular architectures valuable for drug discovery and the manufacturing of fine chemicals. Safety considerations are essential when handling 3-bromochlorobenzene, as it may pose health risks, including skin and eye irritation and potential harm if inhaled. Using appropriate protective equipment and following safety guidelines will minimize exposure risks. In conclusion, 3-bromochlorobenzene is an important compound in organic chemistry due to its reactivity and utility as a precursor in various synthetic pathways. Its role in producing pharmaceuticals, agrochemicals, and specialty chemicals underscores its significance in advancing research and industrial applications, emphasizing the importance of understanding halogenated aromatic compounds in modern chemistry.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C6H4BrCl
Assay 99%
Appearance white powder
CAS No.  108-37-2
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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