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Structure of 437982-59-7
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Tert-butyl 5-amino-3-cyclopropyl-1H-pyrazole-1-carboxylate features a cyclopropyl group enhancing ring rigidity and lipophilicity, while the tert-butyl ester ensures stability and ease of deprotection. The amino substituent at C5 enables direct functionalization in late-stage diversification. This scaffold integrates readily into bioactive molecule design, particularly for kinase inhibitors and GPCR-targeted therapeutics.
Tert-butyl 5-amino-3-cyclopropyl-1H-pyrazole-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyrazole scaffolds. The tert-butyl carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The primary amine supports diverse transformations, including acylation, alkylation, and coupling reactions, while the cyclopropyl substituent enhances metabolic stability and modulates physicochemical properties. This compound functions effectively in standard synthetic workflows for constructing bioactive heterocycles.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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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 : H319-H410
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Precautionary Statements : P264-P273-P280-P391-P501
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Lot numbers can be found on the outside label of a product: