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Structure of 1279090-24-2
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tert-Butyl (3-(4-bromophenyl)oxetan-3-yl)carbamate features a brominated phenyl group attached to an oxetane ring, enabling efficient coupling in Suzuki and other cross-coupling reactions. The tert-butyl carbamate protecting group ensures stability during synthesis and facilitates straightforward deprotection under mild acidic conditions. This compound serves as a key building block for biologically active molecules, particularly in medicinal chemistry applications requiring precise functionalization at the oxetane site.
tert-Butyl (3-(4-bromophenyl)oxetan-3-yl)carbamate serves as a versatile building block in medicinal chemistry, enabling efficient construction of oxetane-containing pharmacophores. The brominated aryl group facilitates palladium-catalyzed cross-coupling reactions, while the oxetane ring provides enhanced metabolic stability and improved solubility. The tert-butyl carbamate protecting group offers excellent bench stability and simplifies purification, making this intermediate ideal for multi-step synthesis workflows requiring functional group tolerance and predictable reactivity.
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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: