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Structure of 1333493-13-2
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(R)-4-((7-Ethyl-8-isopropyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)amino)-3-methoxybenzoic acid features a chiral tetrahydropteridine core with tailored alkyl and methoxy substituents that enhance solubility and metabolic stability. This scaffold integrates readily into bioactive molecule synthesis, offering precise stereochemical control for medicinal chemistry applications.
(R)-4-((7-Ethyl-8-isopropyl-5-methyl-6-oxo-5,6,7,8-tetrahydropteridin-2-yl)amino)-3-methoxybenzoic acid serves as a key heterocyclic building block for pteridine-based medicinal chemistry campaigns. Its functionalized tetrahydropyrimidine core enables straightforward derivatization in standard coupling reactions, while the carboxylic acid and methoxy groups offer orthogonal handles for conjugation. The molecule exhibits bench stability and facilitates purification via standard chromatographic methods, supporting scalable synthesis of targeted 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: