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Structure of 2243590-42-1
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Benzo[1,2-b:3,4-b':5,6-b'']trithiophene-2,5,8-tricarbaldehyde features three aldehyde groups positioned at the 2, 5, and 8 ring junctions of a rigid, electron-deficient fused thiophene core. This configuration enables efficient π-conjugation extension and facilitates directional coupling in organic semiconductor architectures. The aldehyde functionalities serve as reactive handles for imine formation or reductive amination, supporting modular assembly of functionalized donor–acceptor systems.
Benzo[1,2-b:3,4-b':5,6-b'']trithiophene-2,5,8-tricarbaldehyde serves as a versatile tri-functionalized building block for conjugated materials, enabling efficient construction of π-extended architectures via Wittig, Grignard, or reductive amination reactions. Its three aldehyde groups exhibit excellent bench stability and compatibility with diverse functional groups, facilitating modular synthesis of donor-acceptor systems for organic semiconductors and photovoltaic applications.
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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: