CAS 161891-31-2
:(E)-3-(4-bromophenyl)-3-chloro-prop-2-enal
Description:
(E)-3-(4-bromophenyl)-3-chloro-prop-2-enal, with the CAS number 161891-31-2, is an organic compound characterized by its unsaturated aldehyde structure. It features a prop-2-enal backbone, which includes a double bond between the second and third carbon atoms, contributing to its reactivity. The presence of a 4-bromophenyl group indicates that a bromine atom is substituted on the phenyl ring at the para position, which can influence the compound's electronic properties and reactivity. Additionally, the chlorine atom attached to the third carbon enhances its electrophilic character, making it a potential candidate for various chemical reactions, including nucleophilic additions. This compound may exhibit significant biological activity due to its structural features, making it of interest in medicinal chemistry and material science. Its physical properties, such as solubility and boiling point, would depend on the specific molecular interactions and the presence of functional groups. Overall, this compound's unique structure positions it as a valuable entity for further research and application in synthetic chemistry.
Formula:C9H6BrClO
InChI:InChI=1/C9H6BrClO/c10-8-3-1-7(2-4-8)9(11)5-6-12/h1-6H/b9-5+
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