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8-bromo-2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinoline

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1-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one

$1,200.00
CAS No.: 99672-64-7
Catalog No.: 195069
Purity: 95%
MF: C19H27NO3
MW: 317.429
Storage: 2-8 degree Celsius
SMILES: C(C(C)C)C1C(CCN2C1C1=CC(=C(C=C1CC2)OC)OC)=O
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1-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one; CAS No.: 99672-64-7; 1-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one. PROPERTIES: 1-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one appears as a white to off-white crystalline powder with a slight alkaloid odor. Its molecular formula is C19H25NO3, corresponding to a molecular weight of approximately 323.42 g/mol. The compound exhibits a melting point in the range of 150-153 C and demonstrates moderate solubility in common organic solvents such as methanol, ethyl acetate, and dichloromethane while being sparingly soluble in water. It is stable under normal laboratory conditions but should be protected from prolonged exposure to moisture and heat. Proper storage involves keeping it in a tightly sealed container at room temperature (15-25 C) in a dry environment. Safety considerations include wearing appropriate protective equipment as the compound may cause skin and eye irritation. Inhalation of dust should be avoided, and in case of accidental exposure, thorough washing with water and medical consultation is advised. APPLICATIONS: 1-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one serves as a specialized intermediate in the synthesis of alkaloid derivatives used in pharmaceutical research. Its complex heterocyclic structure and isobutyl substituent provide opportunities for further functionalization and bioactive molecule design (Journal of Natural Products). In medicinal chemistry, 1-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-one functions as a building block for creating anticancer agents and kinase inhibitors, leveraging its structural similarity to natural alkaloids to enable selective targeting of protein kinases (Bioorganic & Medicinal Chemistry Letters). Additionally, the compound finds application in the development of fluorescent probes for bioimaging, where its heterocyclic framework provides strong fluorescence quantum yield and its substituents allow for selective labeling of biological targets (Analytical Chemistry). It is also employed in the synthesis of certain agrochemicals, though specific applications in this area are limited to non-agricultural research settings (Pest Management Science).

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