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Structure of 190381-50-1
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This imidazopyrazine derivative features a sterically hindered core with dual methyl groups at the 2- and 6-positions, enhancing metabolic stability. The carboxylic acid moiety enables direct conjugation in peptide coupling workflows, while the electron-deficient heterocycle supports efficient incorporation into bioactive scaffolds under standard conditions.
2,6-Dimethylimidazo[1,2-a]pyrazine-3-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its fused imidazo[1,2-a]pyrazine core provides structural rigidity and enhanced metabolic stability, while the carboxylic acid functionality enables facile derivatization via amide, ester, or amidation reactions. The methyl substituents enhance solubility and facilitate downstream functionalization. This compound exhibits good bench stability and is well-suited for parallel synthesis campaigns targeting kinase inhibitors and other bioactive scaffolds.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: