(Z)-isoquinolin-5(4aH)-one oxime

(Z)-isoquinolin-5(4aH)-one oxime

tert-butyl5-nitro-3,4-dihydroisoquinoline-2(1H)-carboxylate

tert-butyl5-nitro-3,4-dihydroisoquinoline-2(1H)-carboxylate

1-(4-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline

$300.00
CAS No.: 51072-36-7
Catalog No.: WLZ1272
Purity: 95%
MF: C17H23NO
MW: 257.377
Storage: 2-8 degree Celsius
SMILES: COC1=CC=C(C=C1)CC1NCCC=2CCCCC12
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CAS NO.: 51072-36-7; 1-(4-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline. PROPERTIES: This protected amine features a methoxylated benzyl group attached to a fully hydrogenated isoquinoline framework, creating a molecule with potential applications in organic synthesis and medicinal chemistry. The 1-(4-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes a benzyl protecting group that can be selectively removed under acidic or hydrogenolytic conditions to release the amine functionality. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, chemists should wear appropriate personal protective equipment including nitrile gloves and safety goggles. This compound is sensitive to moisture and may form salts upon exposure to atmospheric moisture. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 1-(4-methoxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly those targeting the central nervous system. The octahydroisoquinoline scaffold provides a platform for developing receptor modulators with specific binding profiles. In medicinal chemistry, this compound functions as a building block for creating antidepressant and anxiolytic agents where the protected amine functionality contributes to target engagement. Additionally, the molecule finds utility in chemical biology studies where its defined structure can be used to probe enzyme inhibition mechanisms and cellular signaling pathways. Researchers utilizing this compound benefit from its functional group compatibility, enabling the development of therapeutic agents targeting various disease pathways including neuropsychiatric conditions.

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