6-bromo-1-oxo-2,3-dihydro-1H-indene-4-carboxylic acid

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Reagent Code: #196850
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CAS Number 866848-85-3

science Other reagents with same CAS 866848-85-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.06 g/mol
Formula C₁₀H₇BrO₃
badge Registry Numbers
MDL Number MFCD18647965
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex indene-based scaffolds. Commonly employed in coupling reactions to form bioactive molecules with analgesic and anti-inflammatory properties. Also utilized in research settings for the preparation of enzyme inhibitors and receptor modulators.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿19,630.00

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6-bromo-1-oxo-2,3-dihydro-1H-indene-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex indene-based scaffolds. Commonly employed in coupling reactions to form bioactive molecules with analgesic and anti-inflammatory properties. Also utilized in research settings for the preparation of enzyme

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex indene-based scaffolds. Commonly employed in coupling reactions to form bioactive molecules with analgesic and anti-inflammatory properties. Also utilized in research settings for the preparation of enzyme inhibitors and receptor modulators.

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