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Structure of 159730-72-0
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2-Bromo-4-methyl-5-nitrobenzaldehyde features a bromine atom at the ortho position relative to the aldehyde, combined with a methyl group and a nitro substituent in electron-deficient positions. This configuration enhances reactivity in cross-coupling processes and enables direct incorporation into complex molecular architectures. The aldehyde functionality provides a handle for nucleophilic additions or condensation reactions.
2-Bromo-4-methyl-5-nitrobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of substituted heterocycles via Ullmann or Suzuki coupling reactions. The aldehyde functionality facilitates facile derivatization, while the bromo and nitro groups provide orthogonal handles for cross-coupling and reduction sequences. Its bench-stable crystalline form and compatibility with standard reaction conditions make it well-suited for multi-step synthetic workflows.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: