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ETHYL 5-BROMO-2-CHLOROBENZOATE CAS:76008-73-6

Ethyl 5-bromo-2-chlorobenzoate is an aromatic compound characterized by the presence of both bromine and chlorine substituents on a benzoate structure. With the molecular formula C9H8BrClO2, it features an ethyl ester group that enhances its solubility and reactivity. This compound is of significant interest in organic synthesis due to its potential applications in medicinal chemistry and agrochemical development. Its halogenated structure allows for various substitution reactions, making it a valuable intermediate for synthesizing more complex molecules with diverse biological activities. Consequently, ethyl 5-bromo-2-chlorobenzoate serves as a useful tool in both academic research and industrial applications.


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Application and Effect:

Ethyl 5-bromo-2-chlorobenzoate is an important compound within the realm of organic chemistry, particularly noted for its halogenated aromatic structure. Featuring the molecular formula C9H8BrClO2, this compound consists of a benzoate core substituted with ethyl, bromine, and chlorine groups. The specific positions of these substituents—bromine at the 5-position and chlorine at the 2-position—contribute to the compound's unique chemical properties and reactivity. One of the primary applications of ethyl 5-bromo-2-chlorobenzoate is in organic synthesis, where it serves as a versatile building block for generating more complex organic compounds. The presence of both bromine and chlorine makes it particularly reactive, allowing it to undergo nucleophilic substitution reactions. These reactions can lead to the formation of various derivatives, which may possess desirable pharmacological properties or serve as intermediates in the synthesis of agrochemicals. In medicinal chemistry, halogenated benzoates like ethyl 5-bromo-2-chlorobenzoate are often investigated for their biological activities. Halogens can influence the electronic properties of the molecule, potentially enhancing binding affinities for biological targets. Research has shown that such compounds can exhibit antimicrobial, anti-inflammatory, and anticancer effects, making them relevant for drug discovery efforts. Moreover, the ethyl ester functionality improves the compound's solubility in organic solvents, facilitating its use in reactions and formulations. This characteristic is particularly beneficial when considering the scalability of synthesis processes in industrial settings. Ethyl 5-bromo-2-chlorobenzoate can also be employed in the production of polymeric materials, where its reactive sites can participate in cross-linking or provide functional groups for further modification. This versatility extends its application beyond small-molecule synthesis into material science and polymer chemistry. In conclusion, ethyl 5-bromo-2-chlorobenzoate is a valuable compound in the toolkit of chemists engaged in organic synthesis and pharmaceutical research. Its reactive halogenated structure offers numerous possibilities for creating bioactive molecules and advanced materials, highlighting its importance in both academic and industrial contexts. As research progresses, further understanding of the compound’s properties may lead to innovative applications and derivatives, enriching the landscape of synthetic chemistry.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C9H8BrClO2
Assay 99%
Appearance white powder
CAS No.  76008-73-6
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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