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Structure of 770-31-0
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4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde features a bifunctional scaffold integrating an electron-rich amino group and a reactive aldehyde moiety. This arrangement enables direct coupling in multistep syntheses, particularly useful for constructing heterocyclic frameworks in medicinal chemistry. The methylthio substituent enhances solubility and metabolic stability, while the aldehyde facilitates conjugation under mild conditions.
4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. Its amino and aldehyde functionalities support sequential functionalization, while the methylthio group offers orthogonal reactivity for further derivatization. The compound exhibits good bench stability and facilitates purification via standard chromatographic methods, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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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: