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Structure of 37493-14-4
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(R)-2-Chloropropan-1-ol is a chiral synthon featuring a stereodefined hydroxyl group and a chlorine atom on adjacent carbons. This configuration enables selective functionalization in asymmetric synthesis, particularly in the construction of enantiopure intermediates for pharmaceuticals and agrochemicals. The molecule exhibits enhanced stability under standard handling conditions and integrates readily into multi-step sequences requiring stereocontrol.
(R)-2-Chloropropan-1-ol serves as a valuable chiral building block in synthetic organic chemistry, enabling stereoselective transformations through its reactive primary alcohol and adjacent chiral center. Its bench-stable nature and compatibility with common functional groups facilitate straightforward incorporation into complex molecules, including pharmaceutical intermediates and agrochemical scaffolds. The compound functions effectively in nucleophilic substitution reactions and as a precursor for enantioselective synthesis.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅱ
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Hazard Statements : H226-H302+H312+H332-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: