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Structure of 90221-55-9
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2-Bromo-5-methylbenzaldehyde features a bromine atom at the ortho position relative to the aldehyde group and a methyl substituent at the meta position, creating a sterically accessible, electron-deficient aromatic ring. This configuration enables efficient coupling in cross-coupling reactions and facilitates downstream functionalization in synthetic sequences. The aldehyde functionality provides a reactive handle for nucleophilic additions and condensation chemistry.
2-Bromo-5-methylbenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its compatible bromo and aldehyde functionalities. The methyl group enhances electronic stability and directs ortho-selective functionalization. Its bench-stable nature and compatibility with common protecting groups facilitate efficient synthesis of complex aromatic scaffolds, including those found in pharmaceutical intermediates and agrochemicals.
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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: