ethyl 2-(2-benzoyl-4-methylphenoxy)acetate

95%

Reagent Code: #181014
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CAS Number 72942-62-2

science Other reagents with same CAS 72942-62-2

blur_circular Chemical Specifications

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Weight 298.3 g/mol
Formula C₁₈H₁₈O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of fenbufen and related analogs. It serves as a key building block in pharmaceutical chemistry due to its ability to undergo hydrolysis and cyclization reactions, enabling the formation of biologically active benzoxepine derivatives. Its structure allows for selective modification, making it valuable in developing compounds with improved anti-inflammatory and analgesic properties. Also employed in research settings for structure-activity relationship (SAR) studies of arylpropionic acid-type NSAIDs.

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inventory 1g
10-20 days ฿35,000.00

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ethyl 2-(2-benzoyl-4-methylphenoxy)acetate
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Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of fenbufen and related analogs. It serves as a key building block in pharmaceutical chemistry due to its ability to undergo hydrolysis and cyclization reactions, enabling the formation of biologically active benzoxepine derivatives. Its structure allows for selective modification, making it valuable in developing compounds with improved anti-inflammatory and analgesic properties. Al

Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of fenbufen and related analogs. It serves as a key building block in pharmaceutical chemistry due to its ability to undergo hydrolysis and cyclization reactions, enabling the formation of biologically active benzoxepine derivatives. Its structure allows for selective modification, making it valuable in developing compounds with improved anti-inflammatory and analgesic properties. Also employed in research settings for structure-activity relationship (SAR) studies of arylpropionic acid-type NSAIDs.

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