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Structure of 10133-25-2
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Benzo[b]thiophene-4-carbaldehyde features a fused heterocyclic core with a reactive aldehyde handle at the 4-position. This electron-deficient scaffold integrates readily into synthetic routes requiring planar, π-rich architectures. The aldehyde group enables efficient coupling reactions and functionalization under mild conditions, making it valuable for constructing advanced organic materials and pharmaceutical intermediates.
Benzo[b]thiophene-4-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and coupling reactions with minimal side reactivity. The molecule exhibits excellent bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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: