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*For research and further manufacturing use only, not for direct human use.
Structure of 85977-52-2
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This chiral carboxylic acid features a rigid, fused-ring structure with defined stereochemistry at the 1,2,3,4-tetrahydronaphthalene core. The (S)-configuration imparts distinct spatial orientation essential for asymmetric synthesis. Anchored by a polar carboxyl group, it integrates readily into complex molecular frameworks requiring high enantioselectivity. Bench-stable and moisture-tolerant, this compound enables efficient access to bioactive analogs in medicinal chemistry and natural product synthesis.
(S)-1,2,3,4-Tetrahydronaphthoic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through established functional group transformations. Its rigid, aromatic-fused scaffold provides structural constraint for drug design, while the carboxylic acid functionality facilitates derivatization via amide coupling, esterification, or metal-catalyzed cross-coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in standard synthetic workflows requiring stereochemical control.
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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-H319
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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: