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Structure of 62456-15-9
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trans-Methyl-4-aminocyclohexanecarboxylate features a rigid, conformationally stable cyclohexane scaffold with a trans-configured amino and ester group. This spatial arrangement enhances its utility in asymmetric synthesis and medicinal chemistry, where defined stereochemistry is critical. The molecule exhibits favorable solubility and stability under standard conditions, enabling reliable use in peptide coupling and catalyst design workflows.
trans-Methyl-4-aminocyclohexanecarboxylate serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and peptide-like scaffolds. Its trans-configured cyclohexane ring provides defined stereochemistry, while the amino and ester functionalities offer orthogonal handles for selective derivatization. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for multi-step synthetic sequences 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: