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Structure of 956010-59-6
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5,6-Dihydro-4H-cyclopenta[b]thiophene-2-carbaldehyde features a fused bicyclic core with a reactive aldehyde group, enabling direct functionalization in synthetic routes. The electron-rich thiophene moiety enhances conjugation and reactivity in transition-metal-catalyzed transformations. This bench-stable scaffold integrates readily into complex heterocyclic systems for medicinal chemistry applications.
5,6-Dihydro-4H-cyclopenta[b]thiophene-2-carbaldehyde serves as a versatile heterocyclic building block for medicinal chemistry and materials science. The aldehyde functionality enables direct incorporation into diverse scaffolds via reductive amination, Wittig reactions, or Grignard additions. Its fused thiophene core provides structural rigidity and π-conjugation, while the dihydrocyclopenta ring offers synthetic handle for further functionalization. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to bioactive analogs and conjugated systems in high yield.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P501
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Lot numbers can be found on the outside label of a product: