| Chemical Name: | 4-[(2R)-2-carboxy-1-(2,4-diaminopteridin-6-yl)pent-4-yn-2-yl]benzoic acid |
| CAS Number: | 146464-92-8 |
| Product Number: | AG001E2J(AGN-PC-05IZ1U) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C19H16N6O4 |
| Molecular Weight: | 392.3681 |
4-(2-Carboxy-1-(2,4-diaminopteridin-6-yl)pent-4-yn-2-yl)benzoic acid is a versatile compound commonly employed in chemical synthesis as a key building block for the creation of novel pharmaceuticals, agrochemicals, and materials. This unique molecule plays a crucial role in the field of organic chemistry, particularly in the development of complex structures with specific biological activities.In chemical synthesis, this compound is utilized for its strategic position of functional groups that facilitate the formation of various chemical bonds and enable the introduction of specific stereochemistry in target molecules. Its carboxylic acid functionality serves as a synthetic handle for further derivatization, allowing chemists to modify its structure for the generation of diverse analogs with potential enhanced properties.Furthermore, the structural features of 4-(2-Carboxy-1-(2,4-diaminopteridin-6-yl)pent-4-yn-2-yl)benzoic acid make it a valuable precursor for the construction of biologically active compounds, as it contains moieties known to exhibit interactions with biologically relevant targets. Through strategic modifications and functional group manipulations, this compound can be leveraged to access a wide range of chemical entities with tailored properties for various applications in drug discovery and material science.
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