CAS 4852-91-9
:2-amino-5-(octyloxy)-5-oxopentanoic acid (non-preferred name)
Description:
2-amino-5-(octyloxy)-5-oxopentanoic acid, also known by its CAS number 4852-91-9, is an organic compound characterized by the presence of an amino group, a ketone functional group, and an octyloxy substituent. This compound features a pentanoic acid backbone, which contributes to its acidic properties. The octyloxy group enhances its hydrophobic characteristics, potentially influencing its solubility and interaction with biological membranes. The amino group can participate in hydrogen bonding and may play a role in biological activity, making this compound of interest in various chemical and pharmaceutical applications. Its structure suggests potential uses in drug design or as a biochemical probe, particularly in studies involving amino acid derivatives. The presence of both hydrophilic and hydrophobic regions in its molecular structure may allow it to interact with a variety of biological systems, making it a candidate for further research in medicinal chemistry and biochemistry.
Formula:C13H25NO4
InChI:InChI=1/C13H25NO4/c1-2-3-4-5-6-7-10-18-12(15)9-8-11(14)13(16)17/h11H,2-10,14H2,1H3,(H,16,17)
SMILES:CCCCCCCCOC(=O)CCC(C(=O)O)N
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Found 1 products.
5-Octyl L-Glutamate
CAS:Controlled Product<p>Applications 5-Octyl L-Glutamate is a stable cell-permeable molecule which generates free glutamic acid upon hydrolysis of the ester bond by cytoplasmic esterase.<br>References Chin, R.M., et al.: Nature, 509, 397 (2014)<br></p>Formula:C13H25NO4Color and Shape:NeatMolecular weight:259.34
