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Structure of 1438241-25-8
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cis-3-(Aminomethyl)-1-methylcyclobutanol features a rigid cyclobutane scaffold with complementary stereochemistry, enabling precise spatial positioning of the aminomethyl and methyl groups. This configuration enhances binding affinity in target-directed synthesis. The primary amine facilitates conjugation and derivatization, while the bench-stable structure supports reliable handling under standard conditions.
cis-3-(Aminomethyl)-1-methylcyclobutanol serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of cyclobutane-containing scaffolds with defined stereochemistry. Its pendant primary amine and hydroxyl groups offer orthogonal functionalization potential, facilitating conjugation or derivatization in multi-step syntheses. The compound exhibits good bench stability and is compatible with standard coupling and protection protocols, making it well-suited for use in API development and target-oriented synthesis.
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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: