Ethyl 1-hydroxy-1,3-dimethyl-1H-indene-2-carboxylate

95%

Reagent Code: #180556
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CAS Number 117583-11-6

science Other reagents with same CAS 117583-11-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.28 g/mol
Formula C₁₄H₁₆O₃
thermostat Physical Properties
Boiling Point 364.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.177±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of indomethacin and its analogs. Its structure allows for efficient functionalization at multiple sites, making it valuable in medicinal chemistry for developing compounds with enhanced analgesic and antipyretic properties. It is also employed in research settings to explore new indene-based bioactive molecules, including potential anticancer and antimicrobial agents. The ester group facilitates coupling reactions, while the hydroxyl group can be modified to improve pharmacokinetic profiles in drug design.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿10,490.00
inventory 100mg
10-20 days ฿30,250.00

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Ethyl 1-hydroxy-1,3-dimethyl-1H-indene-2-carboxylate
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Used primarily as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of indomethacin and its analogs. Its structure allows for efficient functionalization at multiple sites, making it valuable in medicinal chemistry for developing compounds with enhanced analgesic and antipyretic properties. It is also employed in research settings to explore new indene-based bioactive molecules, including potential anticancer and antimicrobial agents. Th

Used primarily as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of indomethacin and its analogs. Its structure allows for efficient functionalization at multiple sites, making it valuable in medicinal chemistry for developing compounds with enhanced analgesic and antipyretic properties. It is also employed in research settings to explore new indene-based bioactive molecules, including potential anticancer and antimicrobial agents. The ester group facilitates coupling reactions, while the hydroxyl group can be modified to improve pharmacokinetic profiles in drug design.

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