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CAS 898776-86-8

:

ethyl 6-(3-bromo-4-methyl-phenyl)-6-oxo-hexanoate

Description:
Ethyl 6-(3-bromo-4-methyl-phenyl)-6-oxo-hexanoate is an organic compound characterized by its ester functional group, which is typical of ethyl esters. The presence of a bromo substituent on the aromatic ring indicates that it has halogenated properties, which can influence its reactivity and interaction with other chemical species. The compound features a hexanoate chain, suggesting it has a relatively moderate molecular size, which can affect its solubility and boiling point. The ketone functionality (indicated by the "6-oxo" part of the name) contributes to its potential reactivity, particularly in nucleophilic addition reactions. This compound may exhibit biological activity due to its structural features, making it of interest in medicinal chemistry and synthetic applications. Its specific properties, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the presence of functional groups. Overall, ethyl 6-(3-bromo-4-methyl-phenyl)-6-oxo-hexanoate is a complex molecule with potential applications in various fields of chemistry.
Formula:C15H19BrO3
InChI:InChI=1/C15H19BrO3/c1-3-19-15(18)7-5-4-6-14(17)12-9-8-11(2)13(16)10-12/h8-10H,3-7H2,1-2H3
SMILES:CCOC(=O)CCCCC(=O)c1ccc(C)c(c1)Br
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