3-(Adamantan-1-yl)-6-bromonaphthalen-2-ol

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Reagent Code: #117575
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CAS Number 128272-29-7

science Other reagents with same CAS 128272-29-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.28 g/mol
Formula C₂₀H₂₁BrO
badge Registry Numbers
MDL Number MFCD13182367
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

Used in organic synthesis, particularly in the development of advanced materials and pharmaceuticals. It serves as a key intermediate in the creation of compounds with potential biological activity, such as anti-inflammatory and antiviral agents. Its unique structure, combining adamantane and naphthalene moieties, makes it valuable for designing molecules with specific properties, including enhanced stability and binding affinity. Additionally, it is employed in research focused on fluorescence and photophysical studies due to its aromatic characteristics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,608.00
inventory 1g
10-20 days ฿12,420.00
inventory 100mg
10-20 days ฿2,718.00

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3-(Adamantan-1-yl)-6-bromonaphthalen-2-ol
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Used in organic synthesis, particularly in the development of advanced materials and pharmaceuticals. It serves as a key intermediate in the creation of compounds with potential biological activity, such as anti-inflammatory and antiviral agents. Its unique structure, combining adamantane and naphthalene moieties, makes it valuable for designing molecules with specific properties, including enhanced stability and binding affinity. Additionally, it is employed in research focused on fluorescence and photo

Used in organic synthesis, particularly in the development of advanced materials and pharmaceuticals. It serves as a key intermediate in the creation of compounds with potential biological activity, such as anti-inflammatory and antiviral agents. Its unique structure, combining adamantane and naphthalene moieties, makes it valuable for designing molecules with specific properties, including enhanced stability and binding affinity. Additionally, it is employed in research focused on fluorescence and photophysical studies due to its aromatic characteristics.

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