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Structure of 1381927-79-2
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Methyl (R)-4-(pyrrolidin-2-yl)benzoate hydrochloride features a chiral benzoate core with a pyrrolidin-2-yl substituent, delivering enhanced solubility and stability under standard conditions. This bench-stable derivative serves as a key building block in asymmetric synthesis, enabling efficient access to bioactive scaffolds through straightforward functionalization.
Methyl (R)-4-(pyrrolidin-2-yl)benzoate hydrochloride serves as a chiral building block for the synthesis of bioactive compounds, enabling efficient access to substituted benzoyl motifs. The pyrrolidinyl group provides enhanced solubility and metabolic stability, while the methyl ester offers straightforward derivatization via hydrolysis or nucleophilic substitution. Bench-stable and compatible with standard synthetic protocols, it functions effectively in coupling reactions and heterocycle formation, supporting scalable medicinal chemistry campaigns.
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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: