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Structure of 57203-01-7
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(S)-(Tetrahydrofuran-2-yl)methanol is a chiral building block featuring a hydroxymethyl group attached to the tetrahydrofuran ring. This configuration enables stereoselective transformations in asymmetric synthesis, particularly in the development of complex oxygenated heterocycles. The molecule exhibits favorable solubility in polar organic solvents and maintains stability under standard bench conditions.
(S)-(Tetrahydrofuran-2-yl)methanol serves as a chiral building block for synthesizing bioactive molecules and natural product analogs, leveraging its tetrahydrofuran ring and primary alcohol functionality. The stereogenic center at C-2 enables enantioselective transformations, while the hydroxymethyl group facilitates derivatization via oxidation, protection, or coupling reactions. Its bench-stable nature and compatibility with standard synthetic protocols make it a practical choice for 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-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: