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Structure of 5170-68-3
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2,1,3-Benzothiadiazole-4-carbaldehyde features a rigid heteroaromatic core with an electron-deficient carbonyl group at the 4-position, enabling strong π-conjugation and enhanced charge-transfer properties. This structure supports applications in organic semiconductors and fluorescent probes. The aldehyde moiety facilitates direct functionalization via condensation reactions, streamlining synthesis of advanced materials for optoelectronics and sensing platforms.
2,1,3-Benzothiadiazole-4-carbaldehyde serves as a versatile building block in the synthesis of heterocyclic scaffolds and functionalized dyes. Its aldehyde functionality enables facile imine formation, reductive amination, and coupling reactions under standard conditions. The electron-deficient benzothiadiazole core enhances stability and facilitates π-extended system construction, making it valuable for materials chemistry and medicinal chemistry applications requiring planar, conjugated architectures.
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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: