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Structure of 6850-65-3
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4-Aminocyclohexan-1-ol features a cyclohexane ring bearing both amino and hydroxyl substituents at opposing positions, enabling dual functionalization. This bifunctional scaffold supports conjugation strategies in medicinal chemistry and polymer synthesis. The molecule exhibits enhanced solubility in polar solvents and stability under standard bench conditions, facilitating handling in process development workflows.
4-Aminocyclohexan-1-ol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles and cyclic amine scaffolds. Its bifunctional nature—combining a primary amine and a secondary alcohol—facilitates orthogonal functionalization, protecting group strategies, and macrocyclization. The compound exhibits excellent bench stability and is compatible with standard coupling, reductive amination, and cyclization protocols, making it well-suited for lead optimization and process-scale synthesis.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H314-H410
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Precautionary Statements : P264-P270-P273-P280-P304+P340-P330-P391-P501
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Lot numbers can be found on the outside label of a product: