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Structure of 946426-89-7
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This cyclopropyl-substituted isoxazole methanol features a sterically hindered, electron-deficient core paired with a reactive hydroxymethyl group. The para-dichlorophenyl moiety enhances lipophilicity and metabolic stability, while the cyclopropyl ring contributes conformational rigidity. This structure enables direct incorporation into bioactive scaffolds via coupling reactions under standard conditions.
(5-Cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds. The isoxazole core exhibits robust bench stability and tolerates a range of functional groups, facilitating downstream transformations such as derivatization at the alcohol moiety. Its structural motif is well-documented in medicinal chemistry applications, particularly in the development of kinase inhibitors and CNS-targeted compounds.
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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: