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Structure of 5170-67-2
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Benzo[c][1,2,5]thiadiazole-4,7-dicarbaldehyde features two aldehyde groups flanking a rigid, electron-deficient heterocyclic core. This configuration enables direct conjugation in donor-acceptor architectures, enhancing charge transfer properties for use in organic semiconductors and fluorescent probes. The molecule exhibits high stability under standard handling conditions.
Benzo[c][1,2,5]thiadiazole-4,7-dicarbaldehyde serves as a versatile bifunctional building block for constructing conjugated heterocycles and functional materials. The aldehyde groups enable efficient coupling reactions via imine formation, reductive amination, or Staudinger ligation, while the electron-deficient thiadiazole core enhances π-conjugation and facilitates charge transport. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for modular synthesis of advanced organic semiconductors and bioactive scaffolds.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: