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Structure of 10133-30-9
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5-Formylbenzothiophene serves as a versatile building block in medicinal chemistry and materials science, enabling direct functionalization at the benzothiophene core. The aldehyde group facilitates nucleophilic additions, reductive amination, and condensation reactions, while the thiophene ring provides electronic stability and π-conjugation. Its bench-stable nature and compatibility with common protecting group strategies make it ideal for multi-step synthesis of heterocyclic scaffolds and API intermediates.
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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-H315-H319-H332-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: