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Structure of 167833-10-5
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Methyl (1r,4r)-4-(bromomethyl)cyclohexane-1-carboxylate is a stereochemically defined cyclohexane derivative featuring a bromomethyl group at the 4-position and a methyl ester at the 1-position. This configuration enables selective functionalization in asymmetric synthesis, with the benzylic bromide serving as a reactive handle for nucleophilic substitution. The compound exhibits excellent stability under standard handling conditions and integrates readily into complex molecular architectures.
Methyl (1r,4r)-4-(bromomethyl)cyclohexane-1-carboxylate serves as a versatile chiral building block for cyclohexane-based scaffolds, enabling efficient functionalization via nucleophilic substitution at the bromomethyl position. The stereodefined trans-1,4-cyclohexane framework provides predictable conformational control, while the ester group offers compatibility with standard transformations. Bench-stable and readily purified, it facilitates streamlined synthesis of complex intermediates in medicinal chemistry and natural product derivatization.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: