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Structure of 31486-86-9
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Thieno[3,2-b]thiophene-2-carbaldehyde features a fused heterocyclic core with a reactive aldehyde group at the 2-position. This electron-deficient scaffold integrates readily into conjugated systems, enabling efficient coupling in synthetic routes for organic semiconductors and functional materials. The aldehyde moiety offers direct access to imine derivatives and facilitates further functionalization under mild conditions.
Thieno[3,2-b]thiophene-2-carbaldehyde serves as a versatile building block in the synthesis of conjugated materials and heterocyclic scaffolds. Its aldehyde functionality enables efficient coupling reactions, including Wittig, Horner–Wadman, and reductive amination, facilitating access to functionalized derivatives. The fused thiophene core provides enhanced planarity and electron-rich character, supporting applications in organic semiconductors and photovoltaic materials. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step synthetic sequences.
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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: