CAS 213971-34-7
:1-Naphthalenecarboxylic acid,2,3-dihydroxy-6-methyl-7-(phenylmethyl)-4-propyl-
Description:
1-Naphthalenecarboxylic acid, 2,3-dihydroxy-6-methyl-7-(phenylmethyl)-4-propyl-, identified by CAS number 213971-34-7, is an organic compound characterized by its complex structure, which includes a naphthalene ring system substituted with various functional groups. This compound features a carboxylic acid group, which imparts acidic properties, and multiple hydroxyl groups that contribute to its potential as a hydrogen bond donor and acceptor, enhancing its solubility in polar solvents. The presence of methyl and propyl groups indicates hydrophobic characteristics, while the phenylmethyl substituent adds to its aromatic nature, potentially influencing its reactivity and interactions with other molecules. Such structural features suggest that this compound may exhibit interesting biological activities, making it a candidate for further research in medicinal chemistry or materials science. Its synthesis and applications could be explored in various fields, including pharmaceuticals and organic synthesis, due to the presence of multiple functional groups that allow for diverse chemical reactivity.
Formula:C22H22O4
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Found 4 products.
2,3-Dihydroxy-6-methyl-7-(phenylmethyl)-4-propyl-1-naphthalenecarboxylic Acid
CAS:Controlled Product<p>Applications This compound is used in the synthesis of novel lactate dehydrogenase A inhibitors.This compound is suitable for lactate dehydrogenase (LDH) related research.<br>References Ward, R.A. et al.: J. Med. Chem., 55, 3258 (2012);<br></p>Formula:C22H22O4Color and Shape:NeatMolecular weight:350.41FX-11
CAS:<p>FX-11: potent LDHA inhibitor (Ki 8 μM), activates PKM2, reduces ATP, induces oxidative stress/ROS, cell death, shows antitumor effects.</p>Formula:C22H22O4Purity:98.95%Color and Shape:SolidMolecular weight:350.41
