CAS 4602-83-9
:6,7-Dihydroxy-3,4-Dihydroisoquinoline
Description:
6,7-Dihydroxy-3,4-dihydroisoquinoline is an organic compound characterized by its isoquinoline structure, which features a bicyclic arrangement of carbon atoms. This compound contains two hydroxyl (-OH) groups at the 6 and 7 positions, contributing to its potential reactivity and solubility in polar solvents. The presence of these hydroxyl groups can enhance its ability to participate in hydrogen bonding, influencing its biological activity and interaction with other molecules. Typically, compounds like 6,7-dihydroxy-3,4-dihydroisoquinoline are of interest in medicinal chemistry due to their potential pharmacological properties, including neuroprotective and antioxidant effects. The compound's molecular structure allows it to interact with various biological targets, making it a subject of research in the fields of drug development and biochemical studies. Additionally, its CAS number, 4602-83-9, serves as a unique identifier for regulatory and safety information. Overall, this compound exemplifies the complexity and diversity of organic molecules with potential applications in health sciences.
Formula:C9H9NO2
InChI:InChI=1/C9H9NO2/c11-8-3-6-1-2-10-5-7(6)4-9(8)12/h3-5,10,12H,1-2H2
SMILES:C1CNC=C2C=C(C(=O)C=C12)O
Synonyms:- 6,7-Isoquinolinediol,3,4-dihydro-
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Found 4 products.
6,7-Dihydroxy-3,4-dihydroisoquinoline
CAS:Formula:C9H9NO2Purity:98%Color and Shape:SolidMolecular weight:163.17333,4-dihydroisoquinoline-6,7-diol
CAS:<p>3,4-dihydroisoquinoline-6,7-diol</p>Purity:≥95%Molecular weight:163.17g/mol3,4-Dihydroisoquinoline-6,7-diol Hydrobromide
CAS:Controlled Product<p>Applications 3,4-Dihydroisoquinoline-6,7-diol acts as a reagent for the synthesis of 6,7-dihydroxy-3,4-dihydroisoquinline, a novel inhibitor factore-kB in invitro invasion in murine mammary cells.<br>References Alvarez, F. N., et al.: Chemotherapy, 55, 175 (2009)<br></p>Formula:C9H9NO2·xHBrColor and Shape:NeatMolecular weight:163.17



