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Structure of 1394003-86-1
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This heterocyclic scaffold integrates a pyrazolo[1,5-a]pyrimidine core with complementary amine and carboxylic acid functionalities, enabling direct conjugation in medicinal chemistry. The electron-deficient ring system facilitates selective interactions in target binding studies, while the carboxylic acid group supports derivatization via amidation or esterification under standard conditions.
2-Aminopyrazolo[1,5-a]pyrimidine-3-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its fused pyrazolo-pyrimidine core provides robust scaffold stability and enables efficient functionalization at both the amino and carboxylic acid positions. The molecule facilitates direct coupling reactions, supports diverse derivatization via amide and ester formation, and exhibits favorable solubility and purification characteristics in standard synthetic workflows.
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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: