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Structure of 6089-17-4
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4-Bromobutan-2-ol features a bromine atom at the terminal carbon and a hydroxyl group at the C2 position, creating a bifunctional scaffold ideal for nucleophilic substitution and elimination reactions. This chiral molecule integrates readily into synthetic sequences requiring stereocontrolled functionalization.
4-Bromobutan-2-ol serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized aliphatic chains. Its pendant bromide and secondary alcohol groups exhibit orthogonal reactivity, facilitating sequential transformations such as nucleophilic substitution, cyclization, or protection strategies. The compound demonstrates good bench stability and is readily purified by distillation or chromatography, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 1987
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H315-H319-H335
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Precautionary Statements : P210-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: