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Structure of 364793-86-2
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4-(3-Bromophenethyl)morpholine features a morpholine ring tethered to a brominated phenethyl linker, delivering a versatile scaffold for medicinal chemistry. The para-bromo substitution enhances electrophilic reactivity in cross-coupling processes, while the morpholine moiety provides solubility and hydrogen-bonding capacity. This compound serves as a key intermediate in the synthesis of bioactive molecules, particularly in CNS-targeted drug discovery and kinase inhibitor development.
4-(3-Bromophenethyl)morpholine serves as a versatile building block for medicinal chemistry and materials synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable aryl bromide functionality. The morpholine ring provides polarity and hydrogen-bonding capacity, enhancing solubility and modulating pharmacokinetic properties. Bench-stable and readily purified by column chromatography, it functions efficiently in standard coupling protocols and facilitates the construction of complex heterocyclic scaffolds.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: