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Structure of 2749963-99-1
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This chiral tetrahydrobenzo[b]thiophene scaffold features a strategically positioned amino group, cyano functionality, and methyl-substituted ring system, enabling direct integration into bioactive molecule design. The carboxylic acid moiety provides a handle for conjugation or salt formation. Bench-stable under standard conditions, this compound serves as a high-purity building block for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
(S)-2-Amino-3-cyano-4-methyl-4,5,6,7-tetrahydrobenzo[b]thiophene-4-carboxylic acid serves as a versatile chiral building block for the synthesis of biologically active heterocycles. Its well-defined stereochemistry and complementary functional groups—amino, cyano, carboxylic acid, and methyl—enable diverse transformations including amidation, cyclization, and metal-catalyzed coupling reactions. The molecule exhibits good bench stability and facilitates efficient purification, making it suitable for medicinal chemistry campaigns and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: