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Structure of 40133-07-1
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This tetrahydrobenzo[b]thiophene derivative features a fused bicyclic core with a carboxylic acid handle, offering enhanced solubility and metabolic stability. The saturated thiophene ring imparts conformational rigidity, while the acidic functionality enables direct derivatization for medicinal chemistry applications.
4,5,6,7-Tetrahydrobenzo[b]thiophene-2-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its carboxylic acid functionality enables direct derivatization via amide, ester, or acyl chloride formation, while the saturated thiophene core provides enhanced metabolic stability and tunable lipophilicity. The scaffold exhibits good bench stability and facilitates efficient functional group manipulation in standard coupling protocols.
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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: