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Structure of 1523606-23-6
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cis-3-Amino-1-methylcyclobutan-1-ol hydrochloride features a rigid, stereochemically defined cyclobutane core bearing a primary amine and a methyl group in close spatial proximity. This configuration enables precise molecular recognition in medicinal chemistry applications. The hydrochloride salt enhances solubility and stability under standard handling conditions, facilitating integration into synthetic sequences requiring charged nitrogen functionality.
cis-3-Amino-1-methylcyclobutan-1-ol hydrochloride serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of constrained cyclobutane scaffolds found in bioactive molecules. Its cis-configured amino-alcohol functionality offers predictable stereochemistry and facilitates downstream derivatization via amine alkylation or acylation. The hydrochloride salt enhances crystallinity and shelf stability, simplifying handling and purification. Functions reliably in standard coupling and protection protocols, supporting efficient access to diverse heterocyclic and peptidomimetic architectures.
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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: