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Structure of 1257850-86-4
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tert-Butyl (R)-3-formylmorpholine-4-carboxylate features a chiral morpholine core with a formyl group at the 3-position and a tert-butyl ester at the 4-position. This configuration enables selective functionalization in asymmetric synthesis, where the formyl moiety serves as a reactive handle for C–C bond formation. The molecule exhibits excellent stability under standard bench conditions and compatibility with diverse reaction environments.
tert-Butyl (R)-3-formylmorpholine-4-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling the construction of morpholine-based scaffolds through selective transformations. The formyl group facilitates nucleophilic additions and reductive aminations, while the tert-butyl ester offers stability and ease of removal under mild acidic conditions. Its defined stereochemistry supports asymmetric synthesis, and the molecule exhibits excellent functional group tolerance, making it well-suited for iterative coupling strategies in API development.
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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: