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Structure of 2641451-76-3
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This chiral pyridine derivative features a strategically positioned bromo and iodo substituent, enabling selective cross-coupling reactions. The 1-methoxyethyl group enhances solubility and stability under standard conditions, while the (S)-configuration ensures stereochemical fidelity in asymmetric synthesis workflows.
(S)-3-Bromo-5-iodo-2-(1-methoxyethyl)pyridine serves as a versatile building block for the synthesis of functionalized pyridine derivatives. Its orthogonal halogenation pattern enables sequential cross-coupling reactions, while the methoxyethyl group provides steric and electronic modulation. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for iterative late-stage functionalization in medicinal chemistry 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
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Precautionary Statements : P264-P270-P280-P302+P352-P305+P351+P338-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: