N-(5-Bromo-2-methoxybenzyl)adamantan-1-amine

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Reagent Code: #214884
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CAS Number 332108-65-3

science Other reagents with same CAS 332108-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.29 g/mol
Formula C₁₈H₂₄BrNO
badge Registry Numbers
MDL Number MFCD01826606
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily in organic synthesis as an intermediate for pharmaceutical development, this compound serves as a building block in the creation of bioactive molecules. Its structural features, including the bromo and methoxy groups, allow for further functionalization through cross-coupling reactions, making it valuable in the design of novel therapeutic agents. The adamantane moiety enhances lipophilicity and metabolic stability, which can improve blood-brain barrier penetration—useful in central nervous system-targeted drugs. It has also been explored in medicinal chemistry research for structure-activity relationship (SAR) studies, particularly in the development of receptor ligands and enzyme inhibitors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿11,200.00
inventory 25mg
10-20 days ฿21,200.00
inventory 50mg
10-20 days ฿36,040.00
inventory 100mg
10-20 days ฿61,250.00

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N-(5-Bromo-2-methoxybenzyl)adamantan-1-amine
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Used primarily in organic synthesis as an intermediate for pharmaceutical development, this compound serves as a building block in the creation of bioactive molecules. Its structural features, including the bromo and methoxy groups, allow for further functionalization through cross-coupling reactions, making it valuable in the design of novel therapeutic agents. The adamantane moiety enhances lipophilicity and metabolic stability, which can improve blood-brain barrier penetration—useful in central nervou

Used primarily in organic synthesis as an intermediate for pharmaceutical development, this compound serves as a building block in the creation of bioactive molecules. Its structural features, including the bromo and methoxy groups, allow for further functionalization through cross-coupling reactions, making it valuable in the design of novel therapeutic agents. The adamantane moiety enhances lipophilicity and metabolic stability, which can improve blood-brain barrier penetration—useful in central nervous system-targeted drugs. It has also been explored in medicinal chemistry research for structure-activity relationship (SAR) studies, particularly in the development of receptor ligands and enzyme inhibitors.

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