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Structure of 24078-12-4
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4-Bromo-2-methylbenzaldehyde features a bromine substituent at the para position relative to the aldehyde, combined with a methyl group ortho to the aldehyde. This electron-deficient aromatic scaffold enables direct coupling in cross-coupling reactions and serves as a key intermediate in pharmaceutical synthesis. The aldehyde functionality offers high reactivity for nucleophilic additions and condensation processes.
4-Bromo-2-methylbenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the aldehyde and bromo positions. Its ortho-methyl group provides steric and electronic modulation, enhancing regioselectivity in electrophilic aromatic substitution and cross-coupling reactions. The molecule exhibits good bench stability and facilitates efficient transformations via Suzuki-Miyaura, Negishi, or Stille coupling protocols, making it a practical choice for constructing complex heterocycles and pharmaceutical intermediates.
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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: