5-(4-Isobutoxyphenyl)-1H-pyrrole-2-carboxylic acid

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Reagent Code: #200290
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CAS Number 1542950-01-5

science Other reagents with same CAS 1542950-01-5

blur_circular Chemical Specifications

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Weight 259.30 g/mol
Formula C₁₅H₁₇NO₃
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the design of molecules targeting cyclooxygenase (COX) enzymes, making it valuable in creating non-steroidal anti-inflammatory drugs (NSAIDs). The compound's carboxylic acid and aromatic ether functionalities allow for derivatization to enhance bioavailability and selectivity. It is also employed in medicinal chemistry research for structure-activity relationship (SAR) studies aimed at optimizing therapeutic efficacy and reducing side effects in pain management and inflammatory disease treatments.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,670.00
inventory 250mg
10-20 days ฿9,320.00

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5-(4-Isobutoxyphenyl)-1H-pyrrole-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the design of molecules targeting cyclooxygenase (COX) enzymes, making it valuable in creating non-steroidal anti-inflammatory drugs (NSAIDs). The compound's carboxylic acid and aromatic ether functionalities allow for derivatization to enhance bioavailability and selectivity. It is also employed in medicinal chemistry research for stru

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic compounds. Its structure supports the design of molecules targeting cyclooxygenase (COX) enzymes, making it valuable in creating non-steroidal anti-inflammatory drugs (NSAIDs). The compound's carboxylic acid and aromatic ether functionalities allow for derivatization to enhance bioavailability and selectivity. It is also employed in medicinal chemistry research for structure-activity relationship (SAR) studies aimed at optimizing therapeutic efficacy and reducing side effects in pain management and inflammatory disease treatments.

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