CAS 79082-64-7
:(6S)-6-[(1R)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl]furo[3,4-e][1,3]benzodioxol-8(6H)-one
Description:
The chemical substance with the name "(6S)-6-[(1R)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl]furo[3,4-e][1,3]benzodioxol-8(6H)-one" and CAS number "79082-64-7" is a complex organic compound characterized by its unique structural features, including a furobenzodioxole core and a tetrahydroisoquinoline moiety. This compound exhibits a chiral center, which contributes to its stereochemistry, specifically the (6S) and (1R) configurations. It is likely to possess biological activity due to its structural similarity to various natural products and pharmaceuticals, potentially influencing neurotransmitter systems or exhibiting other pharmacological effects. The presence of methoxy groups suggests possible interactions with biological targets, enhancing lipophilicity and bioavailability. Additionally, the compound may exhibit solubility in organic solvents, with limited solubility in water, typical of many complex organic molecules. Its synthesis and characterization would involve advanced organic chemistry techniques, and it may be of interest in medicinal chemistry research for its potential therapeutic applications.
Formula:C21H21NO6
InChI:InChI=1/C21H21NO6/c1-22-7-6-11-8-15(24-2)16(25-3)9-13(11)18(22)19-12-4-5-14-20(27-10-26-14)17(12)21(23)28-19/h4-5,8-9,18-19H,6-7,10H2,1-3H3/t18-,19+/m1/s1
Synonyms:- Furo(3,4-e)-1,3-benzodioxol-8(6H)-one, 6-((1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-isoquinolinyl)-, (6S)-
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Found 4 products.
(-)-Corlumine
CAS:Corlumine exhibits spasmolytic and GABA antagonist activity.Formula:C21H21NO6Purity:98%Color and Shape:SolidMolecular weight:383.4(-)-Corlumine
CAS:<p>(-)-Crolumine is a synthetic chiral compound, which is derived from natural alkaloids. Its structure is sourced from specific stereochemical modifications of naturally occurring molecules. It operates by interacting with biological targets in a stereospecific manner, exhibiting enantioselective binding properties. This precise mode of action makes it a valuable tool in chiroptical studies, where it aids in analyzing and understanding the stereochemical nature of various compounds.</p>Formula:C21H21NO6Purity:Min. 95%Molecular weight:383.4 g/mol




