CAS 113694-83-0
:disodium (2S)-2-[(pyridin-3-ylcarbonyl)amino]pentanedioate
Description:
Disodium (2S)-2-[(pyridin-3-ylcarbonyl)amino]pentanedioate, with CAS number 113694-83-0, is a chemical compound characterized by its dual sodium salt form, which enhances its solubility in aqueous solutions. This compound features a pentanedioate backbone, indicating the presence of two carboxylate groups, which contribute to its acidic properties. The pyridin-3-ylcarbonyl group attached to the amino functional group suggests that it has potential applications in medicinal chemistry, particularly in drug design, due to the aromatic nature of the pyridine ring that can facilitate interactions with biological targets. The specific stereochemistry indicated by the (2S) configuration implies that the compound has a defined spatial arrangement, which can influence its biological activity and reactivity. Overall, this compound's characteristics, including its solubility, functional groups, and stereochemistry, make it a subject of interest in various fields, including pharmaceuticals and biochemistry.
Formula:C11H10N2Na2O5
InChI:InChI=1/C11H12N2O5.2Na/c14-9(15)4-3-8(11(17)18)13-10(16)7-2-1-5-12-6-7;;/h1-2,5-6,8H,3-4H2,(H,13,16)(H,14,15)(H,17,18);;/q;2*+1/p-2/t8-;;/m0../s1
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L-Glutamic acid, N-nicotinoyl-, disodium salt
CAS:<p>L-Glutamic acid, N-(3-pyridinylcarbonyl)-, disodium salt is a bioactive chemical.</p>Formula:C11H10N2Na2O5Color and Shape:SolidMolecular weight:296.19
